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Publikationer

2023

1. Pulmonary radioaerosol mucociliary clearance assessment: searching for genotype-specific differences and potential as an outcome measure in primary ciliary dyskinesia.
Marthin JK, Holgersen MG, Nielsen KG, Mortensen J.
ERJ Open Res. 2023 Dec 4;9(6):00685-2023. doi: 10.1183/23120541.00685-2023. eCollection 2023 Nov.
PMID: 38076675 Free PMC article.

2. Nationwide lung function monitoring from infancy in newborn-screened children with cystic fibrosis.
Sandvik RM, Schmidt MN, Voldby CM, Buchvald FF, Olesen HV, Olsen J, Kragh MV, Rubak SLM, Pressler T, Robinson PD, Gustafsson PM, Skov M, Nielsen KG.
ERJ Open Res. 2023 Oct 30;9(5):00317-2023. doi: 10.1183/23120541.00317-2023. eCollection 2023 Sep.
PMID: 37908398 Free PMC article.

3. Automatic analysis of bronchus-artery dimensions to diagnose and monitor airways disease in cystic fibrosis.
Lv Q, Gallardo-Estrella L, Andrinopoulou ER, Chen Y, Charbonnier JP, Sandvik RM, Caudri D, Nielsen KG, de Bruijne M, Ciet P, Tiddens H.
Thorax. 2023 Dec 15;79(1):13-22. doi: 10.1136/thorax-2023-220021.
PMID: 37734952

4. Quantitative 99mTc-albumin colloid nasal mucociliary clearance as an outcome in primary ciliary dyskinesia.
Marthin JK, Nielsen KG, Mortensen J.
ERJ Open Res. 2023 Sep 11;9(5):00345-2023. doi: 10.1183/23120541.00345-2023. eCollection 2023 Sep.
PMID: 37701364 Free PMC article.

5. Safety and efficacy of the epithelial sodium channel blocker idrevloride in people with primary ciliary dyskinesia (CLEAN-PCD): a multinational, phase 2, randomised, double-blind, placebo-controlled crossover trial.
Ringshausen FC, Shapiro AJ, Nielsen KG, Mazurek H, Pifferi M, Donn KH, van der Eerden MM, Loebinger MR, Zariwala MA, Leigh MW, Knowles MR, Ferkol TW; CLEAN-PCD investigators and study team.
Lancet Respir Med. 2024 Jan;12(1):21-33. doi: 10.1016/S2213-2600(23)00226-6. Epub 2023 Aug 31.
PMID: 37660715 Clinical Trial.

6. Incidence and aetiology of Danish children with community-acquired pneumonia treated with chest tube drainage in 2022-2023 versus the previous three decades.
Nygaard U, Bloch J, Dungu KHS, Vollmond C, Buchvald FF, Nielsen KG, Kristensen K, Poulsen A, Vissing NH.
Arch Dis Child. 2023 Nov;108(11):945-946. doi: 10.1136/archdischild-2023-326024. Epub 2023 Aug 17.
PMID: 37591515 Free PMC article. No abstract available.

7. Multiple breath washout and oscillometry after allogenic HSCT: a scoping review.
Sonneveld N, Rayment JH, Usemann J, Nielsen KG, Robinson PD.
Eur Respir Rev. 2023 Jul 26;32(169):220251. doi: 10.1183/16000617.0251-2022. Print 2023 Sep 30.
PMID: 37495248 Free PMC article. Review.

8. Exercise capacity in the Danish Fontan population remains stable after ten years of follow-up - is physical activity the key to success?
Ravndal M, Idorn L, Nielsen AKM, Kelly B, Nielsen KG, Nielsen DG, Hjortdal V.
Int J Cardiol. 2023 Sep 15;387:131137. doi: 10.1016/j.ijcard.2023.131137. Epub 2023 Jun 22.
PMID: 37355241

9. Towards the international interoperability of clinical research networks for rare diseases: recommendations from the IRDiRC Task Force.
Nabbout R, Zanello G, Baker D, Black L, Brambilla I, Buske OJ, Conklin LS, Davies EH, Julkowska D, Kim Y, Klopstock T, Nakamura H, Nielsen KG, Pariser AR, Pastor JC, Scarpa M, Smith M, Taruscio D, Groft S.
Orphanet J Rare Dis. 2023 May 9;18(1):109. doi: 10.1186/s13023-023-02650-4.
PMID: 37161573 Free PMC article.

10. Diffuse alveolar haemorrhage in children: an international multicentre study.
Ring AM, Schwerk N, Kiper N, Aslan AT, Aurora P, Ayats R, Azevedo I, Bandeira T, Carlens J, Castillo-Corullon S, Cobanoglu N, Elnazir B, Emiralioğlu N, Eyuboglu TS, Fayon M, Gursoy TR, Hogg C, Kötz K, Karadag B, Látalová V, Krenke K, Lange J, Manali ED, Osona B, Papiris S, Proesmann M, Reix P, Roditis L, Rubak S, Rumman N, Snijders D, Stehling F, Weiss L, Yalcın E, Zirek F, Bush A, Clement A, Griese M, Buchvald FF, Nathan N, Nielsen KG.
ERJ Open Res. 2023 Apr 24;9(2):00733-2022. doi: 10.1183/23120541.00733-2022. eCollection 2023 Mar.
PMID: 37101741 Free PMC article.

11. Nasal nitric oxide measurement in children for the diagnosis of primary ciliary dyskinesia: European Respiratory Society technical standard.
Beydon N, Kouis P, Marthin JK, Latzin P, Colas M, Davis SD, Haarman E, Harris AL, Hogg C, Kilbride E, Kuehni CE, Marangu D, Nielsen KG, Pendergrast C, Robinson P, Rumman N, Rutter M, Walker WT, Ferkol T, Lucas JS.
Eur Respir J. 2023 Apr 20;61(4):2202031. doi: 10.1183/13993003.02031-2022. Print 2023 Apr.
PMID: 36822632

12. High levels of antibodies 6 months after COVID-19 vaccination in children with severe chronic diseases: A prospective longitudinal case series.
Nygaard U, Kirkby NS, Dungu KHS, Nielsen KG, Masmas T, Juul K, Born P, Buus S, Stensballe LG.
Acta Paediatr. 2023 Apr;112(4):802-804. doi: 10.1111/apa.16680. Epub 2023 Feb 2.
PMID: 36695639 No abstract available.

13. Turning lung clearance index on its head. Reference data for SF6 multiple-breath washout derived ventilation distribution efficiency.
Sandvik RM, Lindblad A, Robinson PD, Nielsen KG, Gustafsson P.
J Appl Physiol (1985). 2023 Feb 1;134(2):316-327. doi: 10.1152/japplphysiol.00541.2022. Epub 2022 Dec 22.
PMID: 36548514

14. Parapneumonic effusion in children: Rapid pathogen detection in pleural fluid using multiplex bacterial PCR.
Nygaard U, Kirkby NS, Bloch J, Sethi NJ, Nielsen ACY, Poulsen A, Buchvald F, von Linstow ML, Vissing NH.Acta Paediatr. 2023 Jul;112(7):1555-1557. doi: 10.1111/apa.16768. Epub 2023 Mar 31.PMID: 36946411 No abstract available.

15. Diffuse alveolar hemorrhage in children with interstitial lung disease: Determine etiologies!
Knoflach K, Rapp CK, Schwerk N, Carlens J, Wetzke M, Emiralioğlu N, Kiper N, Ring AM, Buchvald F, Manali E, Papiris S, Reu-Hofer S, Kappler M, Schieber A, Seidl E, Gothe F, Robinson PN, Griese M; ChILD EU Collaborators. Pediatr Pulmonol. 2023 Apr;58(4):1106-1121. doi: 10.1002/ppul.26301. Epub 2023 Jan 13.PMID: 36588100 Free PMC article.

16. Decline in HbA1c during the first year of elexacaftor/tezacaftor/ivacaftor treatment in the Danish cystic fibrosis cohort: Short title: Decline in HbA1c after elexacaftor/tezacaftor/ivacaftor treatment.
Nielsen BU, Olsen MF, Mabuza Mathiesen IH, Pressler T, Ritz C, Katzenstein TL, Olesen HV, Skov M, Jensen-Fangel S, Almdal TP, Faurholt-Jepsen D.J Cyst Fibros. 2023 Nov 20:S1569-1993(23)01676-4. doi: 10.1016/j.jcf.2023.11.005. Online ahead of print.PMID: 37989700 Free article. 
 
17. ALPINE2: Efficacy and safety of 14-day vs 28-day inhaled aztreonam for Pa eradication in children with cystic fibrosis.
Gilchrist FJ, Bui S, Gartner S, McColley SA, Tiddens H, Ruiz G, Stehling F, Alani M, Gurtovaya O, Bresnik M, Watkins TR, Frankovic B, Skov M; ALPINE2 study investigators.J Cyst Fibros. 2023 Jul 14:S1569-1993(23)00821-4. doi: 10.1016/j.jcf.2023.06.008. Online ahead of print.PMID: 37455237 Free article.
 
18. European survey of newborn bloodspot screening for CF: opportunity to address challenges and improve performance.
Munck A, Berger DO, Southern KW, Carducci C, de Winter-de Groot KM, Gartner S, Kashirskaya N, Linnane B, Proesmans M, Sands D, Sommerburg O, Castellani C, Barben J; European CF Society Neonatal Screening Working Group (ECFS NSWG).J Cyst Fibros. 2023 May;22(3):484-495. doi: 10.1016/j.jcf.2022.09.012. Epub 2022 Nov 10.PMID: 36372700

19. Standards for the care of people with cystic fibrosis; establishing and maintaining health.
Southern K, Addy C, Bell S, Bevan A, Borawska U, Brown C, Burgel PR, Button B, Castellani C, Chansard A, Chilvers M, Davies G, Davies J, De Boeck K, Declercq D, Doumit M, Drevinek P, Fajac I, Gartner S, Georgiopoulos A, Gursli S, Gramegna A, Hansen CM, Hug M, Lammertyn E, Landau EEC, Langley R, Mayer-Hamblett N, Middleton A, Middleton P, Mielus M, Morrison L, Munck A, Plant B, Ploeger M, Bertrand DP, Pressler T, Quon BS, Radtke T, Saynor ZL, Shufer I, Smyth AR, Smith C, West NE, van Koningsbruggen-Rietschel S.
J Cyst Fibros. 2023 Dec 20:S1569-1993(23)01727-7. doi: 10.1016/j.jcf.2023.12.002. Online ahead of print.
PMID: 38129255

20. Decline in HbA1c during the first year of elexacaftor/tezacaftor/ivacaftor treatment in the Danish cystic fibrosis cohort: Short title: Decline in HbA1c after elexacaftor/tezacaftor/ivacaftor treatment.
Nielsen BU, Olsen MF, Mabuza Mathiesen IH, Pressler T, Ritz C, Katzenstein TL, Olesen HV, Skov M, Jensen-Fangel S, Almdal TP, Faurholt-Jepsen D.
J Cyst Fibros. 2023 Nov 20:S1569-1993(23)01676-4. doi: 10.1016/j.jcf.2023.11.005. Online ahead of print.
PMID: 37989700

21. Changes in glucose tolerance in people with cystic fibrosis after initiation of first-generation CFTR modulator treatment.
Ekblond RS, Nielsen BU, Højte C, Almdal TP, Shaw J, Pressler T, Faurholt-Jepsen D, Mathiesen IHM.
Pediatr Pulmonol. 2023 Sep;58(9):2600-2609. doi: 10.1002/ppul.26562. Epub 2023 Jun 21.
PMID: 37341613

22. Characterization of impaired beta and alpha cell function in response to an oral glucose challenge in cystic fibrosis: a cross-sectional study.
Nielsen BU, Mathiesen IHM, Møller R, Krogh-Madsen R, Katzenstein TL, Pressler T, Shaw JAM, Ritz C, Rickels MR, Stefanovski D, Almdal TP, Faurholt-Jepsen D.
Front Endocrinol (Lausanne). 2023 Aug 31;14:1249876. doi: 10.3389/fendo.2023.1249876. eCollection 2023.
PMID: 37720541 Free PMC article.

23. Antimicrobial resistance of Pseudomonas aeruginosa in a cystic fibrosis population after introduction of a novel cephalosporin/β-lactamase inhibitor combination.
Katzenstein TL, Faurholt-Jepsen D, Qvist T, Jensen PØ, Pressler T, Johansen HK, Kolpen M.
APMIS. 2023 Aug;131(8):419-425. doi: 10.1111/apm.13331. Epub 2023 Jun 9.
PMID: 37294911

24. The impact of caring on caregivers of patients with life-threatening organ failure.
Kurita GP, Eidemak I, Larsen S, Jeppesen PB, Antonsen LB, Molsted S, Liem YS, Pressler T, Sjøgren P.
Palliat Support Care. 2023 Apr 27:1-7. doi: 10.1017/S1478951523000469. Online ahead of print.
PMID: 37185060

25. Antimicrobial Strategies for Cystic Fibrosis.
Møller R, Pressler T, Qvist T.
Semin Respir Crit Care Med. 2023 Apr;44(2):297-306. doi: 10.1055/s-0042-1758733. Epub 2022 Dec 19.
PMID: 36535665

26. Outcome of elexacaftor/tezacaftor/ivacaftor therapy in patients with cystic fibrosis and solid organ transplantation.
Ørum MB, Rönsholt FF, Jeppesen M, Bendstrup E, Katzenstein TL, Ott P, Perch M, Pressler T, Qvist T, Jensen-Fangel S.
Pediatr Pulmonol. 2023 Feb;58(2):602-605. doi: 10.1002/ppul.26217. Epub 2022 Nov 11.
PMID: 36314653

2022

1. Turning Lung Clearance Index on its Head. Reference Data for SF6 Multiple Breath Washout derived Ventilation Distribution Efficiency (VDE).
Sandvik RM, Lindblad A, Robinson PD, Nielsen KG, Gustafsson PM.
J Appl Physiol (1985). 2022 Dec 22. doi: 10.1152/japplphysiol.00541.2022. Online ahead of print.
PMID: 36548514

2. The disease-specific clinical trial network for primary ciliary dyskinesia: PCD-CTN.
Raidt J, Maitre B, Pennekamp P, Altenburg J, Anagnostopoulou P, Armengot M, Bloemsma LD, Boon M, Borrelli M, Brinkmann F, Carr SB, Carroll MP, Castillo-Corullón S, Coste A, Cutrera R, Dehlink E, Destouches DMS, Di Cicco ME, Dixon L, Emiralioglu N, Erdem Eralp E, Haarman EG, Hogg C, Karadag B, Kobbernagel HE, Lorent N, Mall MA, Marthin JK, Martinu V, Narayanan M, Ozcelik U, Peckham D, Pifferi M, Pohunek P, Polverino E, Range S, Ringshausen FC, Robson E, Roehmel J, Rovira-Amigo S, Santamaria F, Schlegtendal A, Szépfalusi Z, Tempels P, Thouvenin G, Ullmann N, Walker WT, Wetzke M, Yiallouros P, Omran H, Nielsen KG.
ERJ Open Res. 2022 Aug 15;8(3):00139-2022. doi: 10.1183/23120541.00139-2022. eCollection 2022 Jul.
PMID: 35983540 Free PMC article.

3. European survey of newborn bloodspot screening for CF: opportunity to address challenges and improve performance.
Munck A, Berger DO, Southern KW, Carducci C, de Winter-de Groot KM, Gartner S, Kashirskaya N, Linnane B, Proesmans M, Sands D, Sommerburg O, Castellani C, Barben J; 
European CF Society Neonatal Screening Working Group (ECFS NSWG).J Cyst Fibros. 2022 Nov 10:S1569-1993(22)00689-0. doi: 10.1016/j.jcf.2022.09.012. Online ahead of print.

4. Chronic airway disease in primary ciliary dyskinesia-spiced with geno-phenotype associations.
Nielsen KG, Holgersen MG, Crowley S, Marthin JK.
Am J Med Genet C Semin Med Genet. 2022 Mar;190(1):20-35. doi: 10.1002/ajmg.c.31967. Epub 2022 Mar 29.
PMID: 35352480 Free PMC article. Review.

5. Antimicrobial Strategies for Cystic Fibrosis. 
Møller R, Pressler T, Qvist T.
Semin Respir Crit Care Med. 2022 Dec 19. doi: 10.1055/s-0042-1758733. Epub ahead of print. PMID: 36535665.

6. Efficacy and Safety of Elexacaftor/Tezacaftor/Ivacaftor in Children 6 Through 11 Years of Age with Cystic Fibrosis Heterozygous for <i>F508del</i> and a Minimal Function Mutation: A Phase 3b, Randomized, Placebo-controlled Study. 
Mall MA, Brugha R, Gartner S, Legg J, Moeller A, Mondejar-Lopez P, Prais D, Pressler T, Ratjen F, Reix P, Robinson PD, Selvadurai H, Stehling F, Ahluwalia N, Arteaga-Solis E, Bruinsma BG, Jennings M, Moskowitz SM, Noel S, Tian S,Weinstock TG, Wu P, Wainwright CE, Davies JC. 
Am J Respir Crit Care Med. 2022 Dec 1;206(11):1361-1369. doi: 10.1164/rccm.202202-0392OC. PMID: 35816621; PMCID: PMC9746869.

7. Outcome of elexacaftor/tezacaftor/ivacaftor therapy in patients with cystic fibrosis and solid organ transplantation.Ørum MB, Rönsholt FF, Jeppesen M, Bendstrup E, Katzenstein TL, Ott P, Perch M, Pressler T, Qvist T, Jensen-Fangel S. 
Pediatr Pulmonol. 2022 Oct 31. doi:
10.1002/ppul.26217. Epub ahead of print. PMID: 36314653.

8. An international survey on nasal nitric oxide measurement practices for the diagnosis of primary ciliary dyskinesia.
Beydon N, Ferkol T, Harris AL, Colas M, Davis SD, Haarman E, Hogg C, Kilbride E, Kouis P, Kuehni CE, Latzin P, Marangu D, Marthin J, Nielsen KG, Robinson P, Rumman N, Rutter M, Walker W, Lucas JS.
ERJ Open Res. 2022 Apr 4;8(2):00708-2021. doi: 10.1183/23120541.00708-2021. eCollection 2022 Apr.
PMID: 35386825 Free PMC article.

9. Acute exacerbations in children's interstitial lung disease.
Seidl E, Schwerk N, Carlens J, Wetzke M, Emiralioğlu N, Kiper N, Lange J, Krenke K, Szepfalusi Z, Stehling F, Baden W, Hämmerling S, Jerkic SP, Proesmans M, Ullmann N, Buchvald F, Knoflach K, Kappler M; chILD EU collaborators, Griese M. 
Thorax. 2022 Aug;77(8):799-804. doi: 10.1136/thoraxjnl-2021-217941. Epub 2022 Feb 11. PMID:35149584.

10. Lung function from school age to adulthood in primary ciliary dyskinesia.
Halbeisen FS, Pedersen ESL, Goutaki M, Spycher BD, Amirav I, Boon M, Cohen-Cymberknoh M, Crowley S, Emiralioglu N, Haarman EG, Karadag B, Koerner-Rettberg C, Latzin P, Loebinger MR, Lucas JS, Mazurek H, Morgan L, Marthin J, Pohunek P, Santamaria F, Schwerk N, Thouvenin G, Yiallouros P, Nielsen KG, Kuehni CE.
Eur Respir J. 2022 Oct 20;60(4):2101918. doi: 10.1183/13993003.01918-2021. Print 2022 Oct.
PMID: 35301251 Free PMC article.

11. The effect of inhaled hypertonic saline on lung structure in children aged 3-6 years with cystic fibrosis (SHIP-CT): a multicentre, randomised, double-blind, controlled trial.
Tiddens HAWM, Chen Y, Andrinopoulou ER, Davis SD, Rosenfeld M, Ratjen F, Kronmal RA, Hinckley Stukovsky KD, Dasiewicz A, Stick SM; SHIP-CT Study Group.
Lancet Respir Med. 2022 Jul;10(7):669-678. doi: 10.1016/S2213-2600(21)00546-4. Epub 2022 Mar 11.
PMID: 35286860 Clinical Trial.

12. National multi-centre study found a low prevalence of severely impaired lung function in children and adolescents.
Lukić A, Buchvald F, Agertoft L, Rubak S, Skov M, Perch M, Nielsen KG.
Acta Paediatr. 2022 May;111(5):1044-1051. doi: 10.1111/apa.16262. Epub 2022 Jan 31.
PMID: 35051297

13. Increased sputum lactate during oral glucose tolerance test in cystic
fibrosis.
Jensen PØ, Nielsen BU, Kolpen M, Pressler T, Faurholt-Jepsen D, Mathiesen
IHM. 
APMIS. 2022 Aug;130(8):535-539. doi: 10.1111/apm.13233. Epub 2022 May
30. PMID: 35635299; PMCID: PMC9545947.

14. Use of inhaled antibiotics among Danish patients with cystic fibrosis.
Møller R, Nielsen BU, Faurholt-Jepsen D, Katzenstein TL, Skov M, Philipsen
LKD, Pressler T, Johansen HK, Qvist T. 
Pediatr Pulmonol. 2022 Jul;57(7):1726-1734. doi:
10.1002/ppul.25942. Epub 2022 May 14. PMID: 35478387; PMCID: PMC9324817.

15. Adaptive Immune Response to <i>Mycobacterium abscessus</i> Complex
(MABSC) in Cystic Fibrosis and the Implications of Cross-Reactivity.
Mauch RM, Jensen PØ, Qvist T, Kolpen M, Moser C, Pressler T, Nolasco da Silva MT, Høiby N; Copenhagen Study Group on Mycobacterial Infections in Cystic Fibrosis. 
Front Cell
Infect Microbiol. 2022 Apr 20;12:858398. doi: 10.3389/fcimb.2022.858398. PMID:
35548464; PMCID: PMC9084186.

16. Correlates of Pancreatic Enzyme Replacement Therapy Intake in Adults with Cystic Fibrosis: Results of a Cross-Sectional Study. 
Olsen MF, Kjøller-Svarre MS, Møller G, Katzenstein TL, Nielsen BU, Pressler
T, Lewis JI, Mathiesen IH, Mølgaard C, Faurholt-Jepsen D. 
Nutrients. 2022 Mar 22;14(7):1330. doi: 10.3390/nu14071330. PMID: 35405943; PMCID: PMC9003007.

17. Impact of timing of PERT on gastrointestinal symptoms in Danish children and
adolescents with CF. Raun AMT, Brekke G, Mølgaard C, Jaudszus A, Mainz JG, Pressler T, Skov M.
Acta Paediatr. 2022 Feb;111(2):432-439. doi:
10.1111/apa.16143. Epub 2021 Oct 28. PMID: 34626004.

18. Contemporary N2 and SF6 multiple breath washout in infants and toddlers with cystic fibrosis.
Sandvik RM, Gustafsson PM, Lindblad A, Buchvald F, Olesen HV, Olsen JH, Skov M, Schmidt MN, Thellefsen MR, Robinson PD, Rubak S, Pressler T, Nielsen KG.
Pediatr Pulmonol. 2022 Apr;57(4):945-955. doi: 10.1002/ppul.25830. Epub 2022 Jan 25.
PMID: 35029068​

2021

19. A retrospective review of Achromobacter species and antibiotic treatments in patients with primary ciliary dyskinesia.
Holgersen MG, Marthin JK, Johansen HK, Nielsen KG.
Chron Respir Dis. 2021 Jan-Dec;18:14799731211061600. doi: 10.1177/14799731211061600.
PMID: 34854775 Free PMC article.

20. International BEAT-PCD consensus statement for infection prevention and control for primary ciliary dyskinesia in collaboration with ERN-LUNG PCD Core Network and patient representatives.
Marthin JK, Lucas JS, Boon M, Casaulta C, Crowley S, Destouches DMS, Eber E, Escribano A, Haarman E, Hogg C, Maitre B, Marsh G, Martinu V, Moreno-Galdó A, Mussaffi H, Omran H, Pohunek P, Rindlisbacher B, Robinson P, Snijders D, Walker WT, Yiallouros P, Johansen HK, Nielsen KG.
ERJ Open Res. 2021 Aug 2;7(3):00301-2021. doi: 10.1183/23120541.00301-2021. eCollection 2021 Jul.
PMID: 34350277 Free PMC article.

21. Improved agreement between N2 and SF6 multiple-breath washout in healthy infants and toddlers with improved EXHALYZER D sensor performance.
M Sandvik R, Gustafsson PM, Lindblad A, Robinson PD, G Nielsen K.
J Appl Physiol (1985). 2021 Jul 1;131(1):107-118. doi: 10.1152/japplphysiol.00129.2021. Epub 2021 May 27.
PMID: 34043468

22. Current and Future Treatments in Primary Ciliary Dyskinesia.
Paff T, Omran H, Nielsen KG, Haarman EG.
Int J Mol Sci. 2021 Sep 11;22(18):9834. doi: 10.3390/ijms22189834.
PMID: 34575997 Free PMC article. Review.

23. Characteristics and impact of exercise-induced laryngeal obstruction: an international perspective.
Walsted ES, Famokunwa B, Andersen L, Rubak SL, Buchvald F, Pedersen L, Dodd J, Backer V, Nielsen KG, Getzin A, Hull JH.
ERJ Open Res. 2021 Jun 28;7(2):00195-2021. doi: 10.1183/23120541.00195-2021. eCollection 2021 Apr.
PMID: 34195253 Free PMC article.

24. Withdrawal of dornase alfa increases ventilation inhomogeneity in children with cystic fibrosis.
Voldby C, Green K, Philipsen L, Sandvik RM, Skov M, Buchvald F, Pressler T, Nielsen KG.
J Cyst Fibros. 2021 Nov;20(6):949-956. doi: 10.1016/j.jcf.2021.02.004. Epub 2021 Feb 19.
PMID: 33619014 Clinical Trial.

25. National, clinical cohort study of late effects among survivors of acute lymphoblastic leukaemia: the ALL-STAR study protocol.
Andrés-Jensen L, Skipper MT, Mielke Christensen K, Hedegaard Johnsen P, Aagaard Myhr K, Kaj Fridh M, Grell K, Pedersen AML, Leisgaard Mørck Rubak S, Ballegaard M, Hørlyck A, Beck Jensen R, Lambine TL, Gjerum Nielsen K, Tuckuviene R, Skov Wehner P, Klug Albertsen B, Schmiegelow K, Frandsen TL.
BMJ Open. 2021 Feb 9;11(2):e045543. doi: 10.1136/bmjopen-2020-045543.
PMID: 33563628 Free PMC article.
26. Long-term amikacin liposome inhalation suspension in cystic
fibrosis patients with chronic P. aeruginosa infection. Bilton D, Fajac I, Pressler T, Clancy JP, Sands D, Minic P, Cipolli M, Galeva I, Solé A, Quittner AL, Jumadilova Z, Ciesielska M, Konstan MW; CLEAR-110 Study Group. 
J Cyst Fibros. 2021 Nov;20(6):1010-1017. doi: 10.1016/j.jcf.2021.05.013. Epub 2021 Jun 16. PMID:34144923; PMCID: PMC9076322.

27. Maintaining normal lung function in children with cystic fibrosis is possible with aggressive treatment regardless of Pseudomonas aeruginosa infections. 
Hansen CR, Gilljam M, Olesen HV, Høiby N, Karpati F, Johansson E, Krantz C,
Skov M, Pressler T, Lindblad A. 
Acta Paediatr. 2021 Sep;110(9):2607-2609.
doi: 10.1111/apa.15880. Epub 2021 May 5. PMID: 33866605.

28. Triple Therapy for Cystic Fibrosis <i>Phe508del</i>-Gating and -Residual Function Genotypes. Barry PJ, Mall MA, Álvarez A, Colombo C, de Winter-de Groot KM, Fajac I, McBennett KA, McKone EF, Ramsey BW, Sutharsan S, Taylor-Cousar JL, Tullis E, Ahluwalia N, Jun LS, Moskowitz SM, Prieto-Centurion V, Tian S, Waltz D, Xuan F, Zhang Y, Rowe SM, Polineni D; VX18-445-104 Study Group. 
N Engl J Med. 2021 Aug 26;385(9):815-825. doi: 10.1056/NEJMoa2100665. PMID: 34437784;
PMCID: PMC8982185.

29. Associations Between Glucose Tolerance, Insulin Secretion, Muscle and Fat Mass in Cystic Fibrosis. Nielsen BU, Faurholt-Jepsen D, Oturai PS, Qvist T, Krogh-Madsen R, Katzenstein TL, Shaw J, Ritz C, Pressler T, Almdal TP, Mathiesen IHM.
Clin Med Insights Endocrinol Diabetes. 2021 Aug
13;14:11795514211038259. doi: 10.1177/11795514211038259. PMID: 34413690; PMCID:PMC8369959.

30. The BEAT-PCD (Better Experimental Approaches to Treat Primary Ciliary Dyskinesia) Clinical Research Collaboration.
Goutaki M, Crowley S, Dehlink E, Gaupmann R, Horton KL, Kouis P, Lam YT, Loges NT, Lucas JS, Roehmel JF, Shoemark A; BEAT-PCD Clinical Research Collaboration.
Eur Respir J. 2021 Feb 4;57(2):2004601. doi: 10.1183/13993003.04601-2020. Print 2021 Feb.
PMID: 33541936

31. Long-term safety and efficacy of tezacaftor-ivacaftor in individuals with
cystic fibrosis aged 12 years or older who are homozygous or heterozygous for Phe508del CFTR (EXTEND): an open-label extension study. 
Flume PA, Biner RF, Downey DG, Brown C, Jain M, Fischer R, De Boeck K,
Sawicki GS, Chang P, Paz-Diaz H, Rubin JL, Yang Y, Hu X, Pasta DJ, Millar SJ, Campbell D, Wang X, Ahluwalia N, Owen CA, Wainwright CE; VX14-661-110 study group. 
Lancet Respir Med. 2021 Jul;9(7):733-746. doi: 10.1016/S2213-2600(20)30510-5. Epub 2021 Feb 10. Erratum in: Lancet Respir Med. 2021 Apr;9(4):e38. PMID: 33581080.

32. First patient with ILNEB syndrome due to pathogenic variants in ITGA3 surviving to adulthood.
Alstrup M, Marks SD, Ek J, Buchvald F, Lund TK, Perch M, Waters AM, Mogensen
M, Jelsig AM.. Eur J Med Genet. 2021 Nov;64(11):104335. doi: 10.1016/j.ejmg.2021.104335. Epub 2021 Sep 4. PMID: 34492382.

33. Diagnosis and treatment of a multisystemic disorder in children called congenital portosystemic shunts.
Tinning FB, Petersen OBB, Steensberg JN, Buchvald FF, Fallentin E, Rasmussen A, Frevert S, Jørgensen MH. 
Ugeskr Laeger. 2021 Aug 2;183(31):V01210041. Danish. PMID: 34378520.

34. Oliver McFarlane syndrome: two new cases and a review of the literature.
Lisbjerg K, Andersen MKG, Bertelsen M, Brost AG, Buchvald FF, Jensen RB, Bisgaard AM, Rosenberg T, Tümer Z, Kessel L. 
Ophthalmic Genet. 2021 Aug;42(4):464-473. doi: 10.1080/13816810.2021.1904419. Epub 2021 Apr 5. PMID: 33818269.

35. The increased susceptibility to airway infections after preterm birth does not persist into adolescence.
Garioud ALB, Skoven FH, Gregersen R, Lange T, Buchvald F, Greisen G. 
PLoS One. 2020 Sep 3;15(9):e0238382. doi: 10.1371/journal.pone.0238382. Erratum in: PLoS One. 2020 Dec 31;15(12):e0244952. PMID: 32881953; PMCID: PMC7470365.

36. Omics-based tracking of <i>Pseudomonas aeruginosa</i> persistence in
"eradicated" cystic fibrosis patients.
Bartell JA, Sommer LM, Marvig RL, Skov M, Pressler T, Molin S, Johansen HK.
Eur Respir J. 2021 Apr 8;57(4):2000512. doi: 10.1183/13993003.00512-2020. PMID: 33093121; PMCID: PMC8029213.

37. Bacterial Re-Colonization Occurs Early after Lung Transplantation in Cystic
Fibrosis Patients.
Holm AE, Schultz HHL, Johansen HK, Pressler T, Lund TK, Iversen M, Perch M.
J Clin Med. 2021 Mar 19;10(6):1275. doi: 10.3390/jcm10061275.
PMID: 33808547; PMCID: PMC8003282.

38. Transmission and Antibiotic Resistance of <i>Achromobacter</i> in Cystic Fibrosis. 
Gabrielaite M, Bartell JA, Nørskov-Lauritsen N, Pressler T, Nielsen FC,
Johansen HK, Marvig RL. 
J Clin Microbiol. 2021 Mar
19;59(4):e02911-20. doi: 10.1128/JCM.02911-20. PMID: 33472899; PMCID:
PMC8092725.

39. Autologous fibrin sealant co-delivered with antibiotics is a robust method for topical antibiotic treatment after sinus surgery.
Aanaes K, Nielsen KG, Arndal E, von Buchwald C, Pressler T, Høiby N.
Acta Otolaryngol. 2021 Feb;141(2):181-186. doi: 10.1080/00016489.2020.1841909. Epub 2020 Nov 6.
PMID: 33155505

40. Prospective longitudinal association between repeated multiple breath washout measurements and computed tomography scores in children with cystic fibrosis.
Sandvik RM, Kongstad T, Green K, Voldby C, Buchvald F, Skov M, Pressler T, Nielsen KG.
J Cyst Fibros. 2021 Jul;20(4):632-640. doi: 10.1016/j.jcf.2020.09.010. Epub 2020 Oct 4.
PMID: 33028501

2020

41. Extended Screening for Cystic Fibrosis-related Liver Disease Including Elastography in Children and Adolescents.
Højte C, Jørgensen MH, Jensen F, Katzenstein TL, Skov M.
J Pediatr Gastroenterol Nutr. 2020 Nov;71(5):663-668.​

42. Access to medicines for rare diseases: beating the drum for primary ciliary dyskinesia.
Crowley S, Azevedo I, Boon M, Bush A, Eber E, Haarman E, Karadag B, Kötz K, Leigh M, Moreno-Galdó A, Mussaffi H, Nielsen KG, Omran H, Papon JF, Pohunek P, Priftis K, Rindlisbacher B, Santamaria F, Valiulis A, Witt M, Yiallouros P, Zivkovic Z, Kuehni CE, Lucas JS.
ERJ Open Res. 2020 Sep 14;6(3):00377-2020. doi: 10.1183/23120541.00377-2020. eCollection 2020 Jul.
PMID: 32964005 Free PMC article.

43. Proceedings of the 4th BEAT-PCD Conference and 5th PCD Training School.
Gardner LE, Horton KL, Shoemark A, Lucas JS, Nielsen KG, Kobbernagel H, Rubbo B, Hirst RA, Kouis P, Ullmann N, Reula A, Rumman N, Mitchison HM, Pinto A, Richardson C, Schmidt A, Thompson J, Gaupmann R, Dabrowski M, Mill P, Carr SB, Norris DP, Kuehni CE, Goutaki M, Hogg C.
BMC Proc. 2020 Jun 19;14(Suppl 8):7. doi: 10.1186/s12919-020-00191-3. eCollection 2020.
PMID: 32577127 Free PMC article.

44. Lung clearance index-triggered intervention in children with cystic fibrosis - A randomised pilot study.
Voldby C, Green K, Kongstad T, Ring AM, Sandvik RM, Skov M, Buchvald F, Pressler T, Nielsen KG.
J Cyst Fibros. 2020 Nov;19(6):934-941. doi: 10.1016/j.jcf.2020.06.010. Epub 2020 Jun 21.
PMID: 32576447 Clinical Trial.

45. Efficacy and safety of azithromycin maintenance therapy in primary ciliary dyskinesia (BESTCILIA): a multicentre, double-blind, randomised, placebo-controlled phase 3 trial.
Kobbernagel HE, Buchvald FF, Haarman EG, Casaulta C, Collins SA, Hogg C, Kuehni CE, Lucas JS, Moser CE, Quittner AL, Raidt J, Rosthøj S, Sørensen AL, Thomsen K, Werner C, Omran H, Nielsen KG.
Lancet Respir Med. 2020 May;8(5):493-505. doi: 10.1016/S2213-2600(20)30058-8.
PMID: 32380069 Clinical Trial.

46. What it takes to implement regular longitudinal multiple breath washout tests in infants with cystic fibrosis.
Schmidt MN, Sandvik RM, Voldby C, Buchvald FF, Jørgensen MN, Gustafsson P, Skov M, Nielsen KG.
J Cyst Fibros. 2020 Nov;19(6):1027-1028. doi: 10.1016/j.jcf.2020.04.002. Epub 2020 Apr 30.
PMID: 32362559 

47. Lung compartment analysis assessed from N2 multiple-breath washout in children with cystic fibrosis.
Skov L, Green K, Stanojevic S, Jensen R, Buchvald F, Ratjen F, Nielsen KG.
Pediatr Pulmonol. 2020 Jul;55(7):1671-1680. doi: 10.1002/ppul.24773. Epub 2020 Apr 16.
PMID: 32297698

48. Standardised clinical data from patients with primary ciliary dyskinesia: FOLLOW-PCD.
Goutaki M, Papon JF, Boon M, Casaulta C, Eber E, Escudier E, Halbeisen FS, Harris A, Hogg C, Honore I, Jung A, Karadag B, Koerner-Rettberg C, Legendre M, Maitre B, Nielsen KG, Rubbo B, Rumman N, Schofield L, Shoemark A, Thouvenin G, Willkins H, Lucas JS, Kuehni CE.
ERJ Open Res. 2020 Feb 10;6(1):00237-2019. doi: 10.1183/23120541.00237-2019. eCollection 2020 Jan.
PMID: 32055632 Free PMC article.

49. Primary ciliary dyskinesia patients have the same P. aeruginosa clone in sinuses and lungs.
Arndal E, Johansen HK, Haagensen JAJ, Bartell JA, Marvig RL, Alanin M, Aanæs K, Høiby N, Nielsen KG, Backer V, von Buchwald C.
Eur Respir J. 2020 Jan 16;55(1):1901472. doi: 10.1183/13993003.01472-2019. Print 2020 Jan.
PMID: 31558658.

50. SPEF2- and HYDIN-Mutant Cilia Lack the Central Pair-associated Protein SPEF2, Aiding Primary Ciliary Dyskinesia Diagnostics.
Cindrić S, Dougherty GW, Olbrich H, Hjeij R, Loges NT, Amirav I, Philipsen MC, Marthin JK, Nielsen KG, Sutharsan S, Raidt J, Werner C, Pennekamp P, Dworniczak B, Omran H.
Am J Respir Cell Mol Biol. 2020 Mar;62(3):382-396. doi: 10.1165/rcmb.2019-0086OC.
PMID: 31545650

51. The Controversies and Difficulties of Diagnosing Primary Ciliary Dyskinesia.
Shoemark A, Rubbo B, Haarman E, Hirst RA, Hogg C, Jackson CL, Nielsen KG, Papon JF, Robinson P, Walker WT, Lucas JS.
Am J Respir Crit Care Med. 2020 Jan 1;201(1):120-122. doi: 10.1164/rccm.201907-1334LE.
PMID: 31433951 Free PMC article.  

52. Pseudomonas aeruginosa antibody response in cystic fibrosis decreases rapidly following lung transplantation. 
Schwensen HF, Moser C, Perch M, Pressler T, Høiby N. 
J Cyst Fibros. 2020 Jul;19(4):587-594. doi: 10.1016/j.jcf.2020.01.012. Epub 2020 Feb 8. PMID: 32044245.

53. The impact of chest computed tomography and chest radiography on clinical management of cystic fibrosis lung disease.
Bortoluzzi CF, Pontello E, Pintani E, de Winter-de Groot KM, D'Orazio C,
Assael BM, Hunink MGM, Tiddens HAWM, Caudri D; CF Clinics Study Group. 
J Cyst Fibros. 2020 Jul;19(4):641-646. doi: 10.1016/j.jcf.2019.08.005. Epub 2019 Sep 5. PMID: 31494047.

54. Amikacin liposome inhalation suspension for chronic Pseudomonas aeruginosa infection in cystic fibrosis. Bilton D, Pressler T, Fajac I, Clancy JP, Sands D, Minic P, Cipolli M, Galeva I, Solé A, Quittner AL, Liu K, McGinnis JP 2nd, Eagle G, Gupta R, Konstan MW; CLEAR-108 Study Group. 
J Cyst Fibros. 2020
Mar;19(2):284-291. doi: 10.1016/j.jcf.2019.08.001. Epub 2019 Aug 23. PMID:
31451351; PMCID: PMC9078215.

55. Cystic fibrosis newborn screening in Denmark: Experience from
the first 2 years.
Skov M, Baekvad-Hansen M, Hougaard DM, Skogstrand K, Lund AM, Pressler T,
Olesen HV, Duno M.
Pediatr Pulmonol. 2020 Feb;55(2):549-555. doi:10.1002/ppul.24564. Epub 2019 Nov 4. PMID: 31682332.

56. Motile ciliopathies.
Wallmeier J, Nielsen KG, Kuehni CE, Lucas JS, Leigh MW, Zariwala MA, Omran H.
Nat Rev Dis Primers. 2020 Sep 17;6(1):77. doi: 10.1038/s41572-020-0209-6.
PMID: 32943623 Review.

57. Pulmonary function testing in children's interstitial lung disease.
Ring AM, Carlens J, Bush A, Castillo-Corullón S, Fasola S, Gaboli MP, Griese M, Koucky V, La Grutta S, Lombardi E, Proesmans M, Schwerk N, Snijders D, Nielsen KG, Buchvald F.
Eur Respir Rev. 2020 Jul 21;29(157):200019. doi: 10.1183/16000617.0019-2020. Print 2020 Sep 30.
PMID: 32699025 Free PMC article. Review.

58. First case of cystic fibrosis in Greenland - diagnosed by neonatal screening.
Skov M, Koch A, Duno M.
J Cyst Fibros. 2020 May;19(3):e14-e15. doi: 10.1016/j.jcf.2020.02.008

59. Registries and collaborative studies for primary ciliary dyskinesia in Europe.
Ardura-Garcia C, Goutaki M, Carr SB, Crowley S, Halbeisen FS, Nielsen KG, Pennekamp P, Raidt J, Thouvenin G, Yiallouros PK, Omran H, Kuehni CE.
ERJ Open Res. 2020 May 26;6(2):00005-2020. doi: 10.1183/23120541.00005-2020. eCollection 2020 Apr.
PMID: 32494577 Free PMC article. Review.

60. A critical review of definitions used to describe Pseudomonas aeruginosa microbiological status in patients with cystic fibrosis for application in clinical trials. Taccetti G, Denton M, Hayes K; ECFS-CTN Microbiology Group, Drevinek P, Sermet-Gaudelus I. 
J Cyst Fibros. 2020 Jan;19(1):52-67. doi: 10.1016/j.jcf.2019.08.014. Epub 2019 Sep 13. PMID: 31526710.

61. Antisense oligonucleotide eluforsen is safe and improves respiratory symptoms in F508DEL cystic fibrosis. 
Drevinek P, Pressler T, Cipolli M, De Boeck K, Schwarz C, Bouisset F, Boff
M, Henig N, Paquette-Lamontagne N, Montgomery S, Perquin J, Tomkinson N, den
Hollander W, Elborn JS. 
J Cyst Fibros. 2020 Jan;19(1):99-107. doi: 10.1016/j.jcf.2019.05.014. Epub 2019 Jun 7. PMID: 31182369.

62. Bacterial persisters in long-term infection: Emergence and fitness in a complex host environment. 
Bartell JA, Cameron DR, Mojsoska B, Haagensen JAJ, Pressler T, Sommer LM,
Lewis K, Molin S, Johansen HK. 
PLoS Pathog. 2020 Dec 14;16(12):e1009112. doi: 10.1371/journal.ppat.1009112. PMID: 33315938; PMCID:PMC7769609.

63. Patients with cystic fibrosis and advanced lung disease benefit from lumacaftor/ivacaftor treatment. Ejiofor LCK, Mathiesen IHM, Jensen-Fangel S, Olesen HV, Skov M, Philipsen LKD, Pedersen CL, Pressler T. 
Pediatr Pulmonol. 2020 Dec;55(12):3364-3370. doi: 10.1002/ppul.25059. Epub 2020 Sep 19. PMID: 32897653.

64. Inhaled dry powder alginate oligosaccharide in cystic
fibrosis: a randomised, double-blind, placebo-controlled, crossover phase 2b
study. 
van Koningsbruggen-Rietschel S, Davies JC, Pressler T, Fischer R, MacGregor G, Donaldson SH, Smerud K, Meland N, Mortensen J, Fosbøl MØ, Downey DG, Myrset AH, Flaten H, Rye PD. 
ERJ Open Res. 2020 Oct 19;6(4):00132-2020. doi:
10.1183/23120541.00132-2020. PMID: 33123558; PMCID: PMC7569163.

65. Neutrophil count in sputum is associated with increased sputum glucose and sputum L-lactate in cystic fibrosis. 
Nielsen BU, Kolpen M, Jensen PØ, Katzenstein T, Pressler T, Ritz C, Mathiesen IHM, Faurholt-Jepsen D. 
PLoS One. 2020 
Sep 11;15(9):e0238524. doi: 10.1371/journal.pone.0238524. PMID: 32915806; PMCID: PMC7485830.

66. Azole-Resistant Aspergillus fumigatus Among Danish Cystic Fibrosis Patients: Increasing Prevalence and Dominance of TR34/L98H.
Risum M, Hare RK, Gertsen JB, Kristensen L, Johansen HK, Helweg-Larsen J,
Abou-Chakra N, Pressler T, Skov M, Jensen-Fangel S, Arendrup MC. 
Front Microbiol. 2020 Aug
13;11:1850. doi: 10.3389/fmicb.2020.01850. PMID: 32903400; PMCID: PMC7438406.

67. One-year outcomes in a multicentre cohort study of incident rare diffuse parenchymal lung disease in children (ChILD). 
Cunningham S, Graham C, MacLean M, Aurora P, Ashworth M, Barbato A, Calder A, Carlens J, Clement A, Hengst M, Kammer B, Kiper N, Krenke K, Kronfeld K, Lange J, Ley-Zaporozhan J, Nicholson AG, Reu S, Wesselak T, Wetzke M, Bush A, Schwerk N, Griese M; ChILDEU study group. 
Thorax. 2020 Feb;75(2):172-175. doi: 10.1136/thoraxjnl-2019-213217. Epub 2019 Nov 20. PMID: 31748256.

68. European Respiratory Society guideline on long-term management of children with bronchopulmonary dysplasia.
Duijts L, van Meel ER, Moschino L, Baraldi E, Barnhoorn M, Bramer WM, Bolton CE, Boyd J, Buchvald F, Del Cerro MJ, Colin AA, Ersu R, Greenough A, Gremmen C, Halvorsen T, Kamphuis J, Kotecha S, Rooney-Otero K, Schulzke S, Wilson A, Rigau D, Morgan RL, Tonia T, Roehr CC, Pijnenburg MW. 
Eur Respir J. 2020 Jan 2;55(1):1900788. doi: 10.1183/13993003.00788-2019. 
PMID: 31558663

2019

199. Cunningham S, Graham C, MacLean M, Aurora P, Ashworth M, Barbato A, Calder A, Carlens J, Clement A, Hengst M, Kammer B, Kiper N, Krenke K, Kronfeld K, Lange J, Ley-Zaporozhan J, Nicholson AG, Reu S, Wesselak T, Wetzke M, Bush A, Schwerk N, Griese M; ChILDEU study group. One-year outcomes in a multicentre cohort study of incident rare diffuse parenchymal lung disease in children (ChILD). Thorax. 2019 Nov 20. pii: thoraxjnl-2019-213217. doi: 10.1136/thoraxjnl-2019-213217. [Epub ahead of print] PubMed PMID: 31748256.

200. Duijts L, van Meel ER, Moschino L, Baraldi E, Barnhoorn M, Bramer WM, Bolton CE, Boyd J, Buchvald F, Del Cerro MJ, Colin AA, Ersu R, Greenough A, Gremmen C, Halvorsen T, Kamphuis J, Kotecha S, Rooney-Otero K, Schulzke S, Wilson A, Rigau D, Morgan RL, Tonia T, Roehr CC, Pijnenburg MW. European Respiratory Society guideline on long-term management of children with bronchopulmonary dysplasia. Eur Respir J. 2020 Jan 2;55(1). pii: 1900788. doi: 10.1183/13993003.00788-2019. Print 2020 Jan. PubMed PMID: 31558663.

201. Sisman Y, Buchvald FF, Ring AM, Wassilew K, Nielsen KG. Long-Term Lung Function and Exercise Capacity in Postinfectious chILD. Pediatr Allergy Immunol Pulmonol. 2019 Mar 1;32(1):4-11. doi: 10.1089/ped.2018.0973. Epub 2019 Mar 28. PubMed PMID: 31032143; PubMed Central PMCID: PMC6484343.

202. Videbaek K, Buchvald F, Holgersen MG, Henriksen A, Eriksson F, Garred P, Nielsen KG. The impact of mannose-binding lectin polymorphisms on lung function in primary ciliary dyskinesia. Pediatr Pulmonol. 2019 Aug;54(8):1182-1189. doi: 10.1002/ppul.24346. Epub 2019 Apr 22. PubMed PMID: 31012247.

203. Uhlving HH, Skov L, Buchvald F, Heilmann C, Grell K, Ifversen M, Green K, Müller K, Nielsen KG. Lung clearance index for early detection of pulmonary complications after allo-HSCT in children. Pediatr Pulmonol. 2019 Jul;54(7):1029-1038. doi: 10.1002/ppul.24340. Epub 2019 Apr 19. PubMed PMID: 31004401.

204. Kobbernagel HE, Green K, Ring AM, Buchvald FF, Rosthøj S, Gustafsson PM, Nielsen KG. One-year evolution and variability in multiple-breath washout indices in children and young adults with primary ciliary dyskinesia. Eur Clin Respir J. 2019 Mar 26;6(1):1591841. doi: 10.1080/20018525.2019.1591841. eCollection 2019. PubMed PMID: 30949311; PubMed Central PMCID: PMC6442098.

205. Skov M, Baekvad-Hansen M, Hougaard DM, Skogstrand K, Lund AM, Pressler T, Olesen HV, Duno M. Cystic fibrosis newborn screening in Denmark: Experience from the first 2 years. Pediatr Pulmonol. 2019 Nov 4. doi: 10.1002/ppul.24564. [Epub ahead of print]

206. Pedersen MG, Højte C, Olesen HV, Pressler T, Skov M. Late diagnosis and poor nutrition in cystic fibrosis diagnosed before implementation of newborn screening. Acta Paediatr. 2019 Dec;108(12):2241-2245. doi: 10.1111/apa.14908. Epub 2019 Jul 12.

207. Mathiesen IH, Hitz MF, Katzenstein TL, Oturai P, Skov M, Jørgensen NR, Jensen PO, Mikkelsen CR, Krogh-Madsen R, Pressler T, Faurholt-Jepsen D. Markers of bone turnover are reduced in patients with CF related diabetes; the role of glucose. J Cyst Fibros. 2019 May;18(3):436-441. doi: 10.1016/j.jcf.2019.01.004. Epub 2019 Mar 28.

208. Hengzhuang W, Green K, Pressler T, Skov M, Katzenstein TL, Wu X, Høiby N. Optimization of colistin dosing regimen for cystic fibrosis patients with chronic Pseudomonas aeruginosa biofilm lung infections. Pediatr Pulmonol. 2019 May;54(5):575-580. doi: 10.1002/ppul.24269. Epub 2019 Feb 25.

209. Skov M, Hansen CR, Pressler T. Cystic fibrosis - an example of personalized and precision medicine. APMIS. 2019 May;127(5):352-360. doi: 10.1111/apm.12915. Epub 2019 Feb 14. Review.

210. Ravnholt C, Qvist T, Kolpen M, Pressler T, Skov M, Høiby N. Antibody response against Mycobacterium avium complex in cystic fibrosis patients measured by a novel IgG ELISA test. J Cyst Fibros. 2019 Jul;18(4):516-521. doi: 10.1016/j.jcf.2018.11.011. Epub 2018 Nov 29.

211. Taccetti G, Denton M, Hayes K; ECFS-CTN Microbiology Group, Drevinek P, Sermet-Gaudelus I. A critical review of definitions used to describe Pseudomonas aeruginosa microbiological status in patients with cystic fibrosis for application in clinical trials. J Cyst Fibros. 2019 Sep 13. pii: S1569-1993(19)30867-7. doi: 10.1016/j.jcf.2019.08.014. [Epub ahead of print] PubMed PMID: 31526710.

212. Bortoluzzi CF, Pontello E, Pintani E, de Winter-de Groot KM, D'Orazio C, Assael BM, Hunink MGM, Tiddens HAWM, Caudri D; CF Clinics Study Group. The impact of chest computed tomography and chest radiography on clinical management of cystic fibrosis lung disease. J Cyst Fibros. 2019 Sep 4. pii: S1569-1993(19)30837-9. doi: 10.1016/j.jcf.2019.08.005. [Epub ahead of print] PubMed PMID: 31494047.

213. Bilton D, Pressler T, Fajac I, Clancy JP, Sands D, Minic P, Cipolli M, Galeva I, Solé A, Quittner AL, Liu K, McGinnis JP 2nd, Eagle G, Gupta R, Konstan MW; CLEAR-108 Study Group. Amikacin liposome inhalation suspension for chronic Pseudomonas aeruginosa infection in cystic fibrosis. J Cyst Fibros. 2019 Aug 23. pii: S1569-1993(19)30833-1. doi: 10.1016/j.jcf.2019.08.001. [Epub ahead of print] PubMed PMID: 31451351.

214. Drevinek P, Pressler T, Cipolli M, De Boeck K, Schwarz C, Bouisset F, Boff M, Henig N, Paquette-Lamontagne N, Montgomery S, Perquin J, Tomkinson N, den Hollander W, Elborn JS. Antisense oligonucleotide eluforsen is safe and improves respiratory symptoms in F508DEL cystic fibrosis. J Cyst Fibros. 2019 Jun 7. pii: S1569-1993(19)30766-0. doi: 10.1016/j.jcf.2019.05.014. [Epub ahead of print] PubMed PMID: 31182369.

215. Hengzhuang W, Green K, Pressler T, Skov M, Katzenstein TL, Wu X, Høiby N. Optimization of colistin dosing regimen for cystic fibrosis patients with chronic Pseudomonas aeruginosa biofilm lung infections. Pediatr Pulmonol. 2019 May;54(5):575-580. doi: 10.1002/ppul.24269. Epub 2019 Feb 25. PubMed PMID: 30803159.

216. Qvist T, Schlüter DK, Rajabzadeh V, Diggle PJ, Pressler T, Carr SB,´Taylor-Robinson D. Seasonal fluctuation of lung function in cystic fibrosis: A national register-based study in two northern European populations. J Cyst Fibros. 2019 May;18(3):390-395. doi: 10.1016/j.jcf.2018.10.006. Epub 2018 Oct 19. PubMed PMID: 30343891; PubMed Central PMCID: PMC6559396.

217. Schlüter DK, Griffiths R, Adam A, Akbari A, Heaven ML, Paranjothy S, Nybo Andersen AM, Carr SB, Pressler T, Diggle PJ, Taylor-Robinson D. Impact of cystic fibrosis on birthweight: a population based study of children in Denmark and Wales. Thorax. 2019 May;74(5):447-454. doi: 10.1136/thoraxjnl-2018-211706. Epub 2018 Jul 19. PubMed PMID: 30026297; PubMed Central PMCID: PMC6484694.

218. Cindrić S, Dougherty GW, Olbrich H, Hjeij R, Loges NT, Amirav I, Philipsen MC, Marthin JK, Nielsen KG, Sutharsan S, Raidt J, Werner C, Pennekamp P, Dworniczak B, Omran H. SPEF2- and HYDIN-mutant Cilia Lack the Central Pair Associated Protein SPEF2 Aiding PCD Diagnostics. Am J Respir Cell Mol Biol. 2019 Sep 23. doi: 10.1165/rcmb.2019-0086OC. [Epub ahead of print] PMID: 31545650 [PubMed - as supplied by publisher]

219. Kouis P, Goutaki M, Halbeisen FS, Gioti I, Middleton N, Amirav I; Israeli PCD Consortium, Barbato A; Italian PCD Consortium, Behan L, Boon M, Emiralioglu N, Haarman EG, Karadag B, Koerner-Rettberg C, Lazor R; Swiss PCD Group, Loebinger MR, Maitre B; French Reference Centre for Rare Lung Diseases, Mazurek H, Morgan L, Nielsen KG, Omran H, Özçelik U, Price M, Pogorzelski A, Snijders D; PCD Italian Consortium, Thouvenin G; French Reference Centre for Rare Lung Diseases, Werner C, Zivkovic Z, Kuehni CE, Yiallouros PK. Prevalence and course of disease after lung resection in primary ciliary dyskinesia: a cohort & nested case-control study. Respir Res. 2019 Sep 18;20(1):212. doi: 10.1186/s12931-019-1183-y. PMID: 31533829 [PubMed - in process] Free PMC Article

220. Shoemark A, Rubbo B, Haarman E, Hirst RA, Hogg C, Jackson CL, Nielsen KG, Papon JF, Robinson P, Walker WT, Lucas JS. The Controversies and Difficulties of Diagnosing Primary Ciliary Dyskinesia. Am J Respir Crit Care Med. 2020 Jan 1;201(1):120-122. doi: 10.1164/rccm.201907-1334LE. No abstract available. PMID: 31433951 [PubMed - in process] Free PMC Article

221. Holgersen MG, Marthin JK, Nielsen KG. Proof of Concept: Very Rapid Tidal Breathing Nasal Nitric Oxide Sampling Discriminates Primary Ciliary Dyskinesia from Healthy Subjects. Lung. 2019 Apr;197(2):209-216. doi: 10.1007/s00408-019-00202-x. Epub 2019 Feb 14. PMID: 30762092 [PubMed - in process]

222. Lucas JS, Gahleitner F, Amorim A, Boon M, Brown P, Constant C, Cook S, Crowley S, Destouches DMS, Eber E, Mussaffi H, Haarman E, Harris A, Koerner-Rettberg C, Kuehni CE, Latzin P, Loebinger MR, Lorent N, Maitre B, Moreno-Galdó A, Nielsen KG, Özçelik U, Philipsen LKD, Pohunek P, Polverino E, Rademacher J, Robinson P, Snijders D, Yiallouros P, Carr SB. Pulmonary exacerbations in patients with primary ciliary dyskinesia: an expert consensus definition for use in clinical trials. ERJ Open Res. 2019 Feb 1;5(1). pii: 00147-2018. doi: 10.1183/23120541.00147-2018. eCollection 2019 Feb. PMID: 30723730 [PubMed] Free PMC Article

223. Crowley S, Holgersen MG, Nielsen KG. Variation in treatment strategies for the eradication of Pseudomonas aeruginosa in primary ciliary dyskinesia across European centers. Chron Respir Dis. 2019 Jan-Dec;16:1479972318787919. doi: 10.1177/1479972318787919. Epub 2018 Jul 18. PMID: 30021461 [PubMed - in process] Free PMC Article

224. Nothe-Menchen, Tabea; Wallmeier, Julia MD; Pennekamp, Petra PhD; Hoben, Inga M. PhD; Olbrich, Heike PhD; Loges, Niki T. PhD; Raidt, Johanna MD; Dougherty, Gerard W. PhD; Hjeij, Rim PhD; Dworniczak, Bernd PhD; Omran, Heymut MD; the PCD study group*; Amirav, Israel MD; Biebach, Luisa MD; Fabricius, Dorit MD; Griese, Matthias MD; Gro[latin sharp s]e-Onnebrink, Jorg MD; Haffner, Karsten MD; Hector, Andreas MD; Jung, Andreas MD; Kaiser-Labusch, Petra MD; Kaiser, Thomas MD; Ke[latin sharp s]ler, Christina MD; Kitz, Richard MD; Knowles, Michael R. MD; Koerner-Rettberg, Cordula MD; Kristoffersson, Ulf MD, PhD; Leigh, Margaret W. MD; Mertsch, Pontus MD; Mischo, Bernhard MD; Nielsen, Kim G.; Poeta, Marco MD; Rietschel, Ernst MD; Roth, Samra MD; Santamaria, Francesca MD; Schmalstieg, Christian MD; Schmidts, Miriam MD; Schwarz, Carsten MD; Schwerk, Nicolaus MD; Seithe, Horst MD; Tebbe, Johannes MD; Werner, Claudius MD; Zariwala, Maimoona A. Randomization of Left-Right Asymmetry and Congenital Heart Defects: The Role of DNAH5 in Humans and Mice Circulation: Genomic and Precision Medicine Issue: Volume 12(11), November 2019, p e002686 DOI: 10.1161/CIRCGEN.119.002686

2018

176. Lung function in patients with primary ciliary dyskinesia: an iPCD Cohort study.

Halbeisen FS, Goutaki M, Spycher BD, Amirav I, Behan L, Boon M, Hogg C, Casaulta C, Crowley S, Haarman EG, Karadag B, Koerner-Rettberg C, Loebinger MR, Mazurek H, Morgan L, Nielsen KG, Omran H, Santamaria F, Schwerk N, Thouvenin G, Yiallouros P, Lucas JS, Latzin P, Kuehni CE.
Eur Respir J. 2018 Aug 23;52(2). pii: 1801040. doi: 10.1183/13993003.01040-2018. Print 2018 Aug.
PMID: 30049738 [PubMed - in process]

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177. Variability of monthly nitrogen multiple-breath washout during one year in children with cystic fibrosis.
Green K, Kongstad T, Skov M, Buchvald F, Rosthøj S, Marott JL, Gustafsson P, Pressler T, Nielsen KG.
J Cyst Fibros. 2018 Mar;17(2):242-248. doi: 10.1016/j.jcf.2017.11.007. Epub 2017 Dec 19.
PMID: 29273421 [PubMed - in process]

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178. The effect of time-of-day and chest physiotherapy on multiple breath washout measures in children with clinically stable cystic fibrosis.
Voldby C, Green K, Rosthøj S, Kongstad T, Philipsen L, Buchvald F, Skov M, Pressler T, Gustafsson P, Nielsen KG.
PLoS One. 2018 Jan 10;13(1):e0190894. doi: 10.1371/journal.pone.0190894. eCollection 2018.
PMID: 29320566 [PubMed - indexed for MEDLINE] Free PMC Article

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179. Preschool Multiple-Breath Washout Testing. An Official American Thoracic Society Technical Statement.
Robinson PD, Latzin P, Ramsey KA, Stanojevic S, Aurora P, Davis SD, Gappa M, Hall GL, Horsley A, Jensen R, Lum S, Milla C, Nielsen KG, Pittman JE, Rosenfeld M, Singer F, Subbarao P, Gustafsson PM, Ratjen F; ATS Assembly on Pediatrics.
Am J Respir Crit Care Med. 2018 Mar 1;197(5):e1-e19. doi: 10.1164/rccm.201801-0074ST.
PMID: 29493315 [PubMed - in process]

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180. The accessibility of topical treatment in the paranasal sinuses on operated cystic fibrosis patients assessed by scintigraphy.
Aanaes K, Alanin MC, Nielsen KG, Moller Jorgensen M, von Buchwald C, Hoiby N, Johansen HK, Johannesen HH, Mortensen J.
Rhinology. 2018 Sep 1;56(3):268-273. doi: 10.4193/Rhin17.243.
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181. Mutations in C11orf70 Cause Primary Ciliary Dyskinesia with Randomization of Left/Right Body Asymmetry Due to Defects of Outer and Inner Dynein Arms.
Höben IM, Hjeij R, Olbrich H, Dougherty GW, Nöthe-Menchen T, Aprea I, Frank D, Pennekamp P, Dworniczak B, Wallmeier J, Raidt J, Nielsen KG, Philipsen MC, Santamaria F, Venditto L, Amirav I, Mussaffi H, Prenzel F, Wu K, Bakey Z, Schmidts M, Loges NT, Omran H.
Am J Hum Genet. 2018 May 3;102(5):973-984. doi: 10.1016/j.ajhg.2018.03.025.
PMID: 29727693 [PubMed - indexed for MEDLINE] Free PMC Article 

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182. Initiating transitional care for adolescents with cystic fibrosis at the age of 12 is both feasible and promising.
Skov M, Teilmann G, Damgaard IN, Nielsen KG, Hertz PG, Holgersen MG, Presfeldt M, Dalager AMS, Brask M, Boisen KA.
Acta Paediatr. 2018 Nov;107(11):1977-1982. doi: 10.1111/apa.14388. Epub 2018 May 29.
PMID: 29729195 [PubMed - in process]

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183. Associations of physical activity with childhood asthma, a population study based on the WHO - health behaviour in school-aged children survey.
Lochte L, Petersen PE, Nielsen KG, Andersen A, Platts-Mills TAE.
Asthma Res Pract. 2018 Apr 30;4:6. doi: 10.1186/s40733-018-0042-9. eCollection 2018.
PMID: 29736253 [PubMed] Free PMC Article

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184. Infant nasal nitric oxide over time: natural evolution and impact of respiratory tract infection.
Marthin JK, Philipsen MC, Rosthoj S, Nielsen KG.
Eur Respir J. 2018 Jun 21;51(6). pii: 1702503. doi: 10.1183/13993003.02503-2017. Print 2018 Jun.
PMID: 29748307 [PubMed - in process]

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185. Fitness and lung function in children with primary ciliary dyskinesia and cystic fibrosis.
Ring AM, Buchvald FF, Holgersen MG, Green K, Nielsen KG.
Respir Med. 2018 Jun;139:79-85. doi: 10.1016/j.rmed.2018.05.001. Epub 2018 May 3.
PMID: 29858006 [PubMed - indexed for MEDLINE]

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186. Ventilation inhomogeneity and NO and CO diffusing capacity in ex-premature school children.
Sørensen JK, Buchvald F, Berg AK, Robinson PD, Nielsen KG.
Respir Med. 2018 Jul;140:94-100. doi: 10.1016/j.rmed.2018.06.006. Epub 2018 Jun 6.
PMID: 29957288 [PubMed - indexed for MEDLINE]

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187. Variation in treatment strategies for the eradication of Pseudomonas aeruginosa in primary ciliary dyskinesia across European centers.
Crowley S, Holgersen MG, Nielsen KG.
Chron Respir Dis. 2019 Jan-Dec;16:1479972318787919. doi: 10.1177/1479972318787919. Epub 2018 Jul 18.
PMID: 30021461 [PubMed - in process]

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188. The increased purchase of asthma medication for individuals born preterm seems to wane with age: A register-based longitudinal national cohort study.
Damgaard ALB, Gregersen R, Lange T, Buchvald F, Hansen BM, Greisen G.
PLoS One. 2018 Jul 5;13(7):e0199884. doi: 10.1371/journal.pone.0199884. eCollection 2018.
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189. Antibody response against Mycobacterium avium complex in cystic fibrosis patients measured by a novel IgG ELISA test.
Ravnholt C, Qvist T, Kolpen M, Pressler T, Skov M, Høiby N.
J Cyst Fibros. 2018 Nov 29. pii: S1569-1993(18)30938-X. doi: 10.1016/j.jcf.2018.11.011. [Epub ahead of print]
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190. The importance of early diagnosis of Mycobacterium abscessus complex in patients with cystic fibrosis.
Ravnholt C, Kolpen M, Skov M, Moser C, Katzenstein TL, Pressler T, Høiby N, Qvist T.
APMIS. 2018 Dec;126(12):885-891. doi: 10.1111/apm.12903. Review.
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16. 191. Osteoporosis Is Associated with Deteriorating Clinical Status in Adults with Cystic Fibrosis.
Mathiesen IH, Pressler T, Oturai P, Katzenstein TL, Skov M, Frikke-Schmidt R, Hitz MF.
Int J Endocrinol. 2018 Mar 26;2018:4803974. doi: 10.1155/2018/4803974. eCollection 2018.
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192. Living with cystic fibrosis - a qualitative study of a life coaching intervention.
Knudsen KB, Boisen KA, Katzenstein TL, Mortensen LH, Pressler T, Skov M, Jarden M.
Patient Prefer Adherence. 2018 Apr 19;12:585-594. doi: 10.2147/PPA.S159306. eCollection 2018.
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193. Seasonal fluctuation of lung function in cystic fibrosis: A national register-based study in two northern European populations.
Qvist T, Schlüter DK, Rajabzadeh V, Diggle PJ, Pressler T, Carr SB, Taylor-Robinson D.
J Cyst Fibros. 2018 Oct 18. pii: S1569-1993(18)30858-0. doi: 10.1016/j.jcf.2018.10.006. [Epub ahead of print]
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19. 194. Impact of cystic fibrosis on birthweight: a population based study of children in Denmark and Wales.
Schlüter DK, Griffiths R, Adam A, Akbari A, Heaven ML, Paranjothy S, Nybo Andersen AM, Carr SB, Pressler T, Diggle PJ, Taylor-Robinson D.
Thorax. 2018 Jul 19. pii: thoraxjnl-2018-211706. doi: 10.1136/thoraxjnl-2018-211706. [Epub ahead of print]
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20. 195. The choice of lung function reference equation affects clinical trial eligibility: Results from a cystic fibrosis cohort.
Mathiesen IH, Ronit A, Pressler T.
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21. 196. Aquagenic wrinkling of the palms in patients with cystic fibrosis.
Kaiser H, Brustad N, Pressler T, Bygum A.
Br J Dermatol. 2018 Aug;179(2):494-495. doi: 10.1111/bjd.16448. Epub 2018 May 6. No abstract available.
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197. Prevalence and characteristics of chronic kidney disease among Danish adults with cystic fibrosis.
Berg KH, Ryom L, Faurholt-Jepsen D, Pressler T, Katzenstein TL.
J Cyst Fibros. 2018 Jul;17(4):478-483. doi: 10.1016/j.jcf.2017.11.001. Epub 2017 Dec 1.
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198. Proceedings of the 3rd BEAT-PCD Conference and 4th PCD Training School
Hannah Farley, Bruna Rubbo, Zuzanna Bukowy-Bieryllo, Mahmoud Fassad, Myrofora Goutaki, Katharine Harman, Claire Hogg, Claudia E. Kuehni, Susana Lopes, Kim G. Nielsen, Dominic P. Norris, Ana Reula, Nisreen Rumman, Amelia Shoemark, Hannah Wilkins, Agatha Wisse, Jane S. Lucas and June K. Marthin.

BMC Proceedings 2018 12 (Suppl 16) :64

2017

160.  Qvist T, Pressler T, Katzenstein TL, Høiby N, Collins MT. Evaluation of a bovine antibody test for diagnosing Mycobacterium avium complex in patients with cystic fibrosis. Pediatr Pulmonol. 2017 Jan;52(1):34-40. doi: 10.1002/ppul.23608.

 

161. Alanin MC, Aanaes K, Høiby N, Pressler T, Skov M, Nielsen KG, Johansen HK, von Buchwald C.

Sinus surgery can improve quality of life, lung infections, and lung function in patients with primary ciliary dyskinesia

Int Forum Allergy Rhinol. 2017 Mar;7(3):240-247. doi: 10.1002/alr.21873. Epub 2016 Nov 23.

 

162. Waldmann, E., D. Taylor-Robinson, N. Klein, T. Kneib, T. Pressler, M. Schmid and A. Mayr (2017). "Boosting joint models for longitudinal and time-to-event data." Biom J.  2017 Mar 21. doi: 10.1002/bimj.201600158. [Epub ahead of print]

           

163. Marthin JK, Stevens EM, Larsen LA, Christensen ST, Nielsen KG.

Patient-specific three-dimensional explant spheroids derived from human nasal airway epithelium: a simple methodological approach for ex vivo studies of primary ciliary dyskinesia.

Cilia. 2017 Mar 23;6:3. doi: 10.1186/s13630-017-0049-5. eCollection 2017.

 

164. Høiby N, Bjarnsholt T, Moser C, Jensen PØ, Kolpen M, Qvist T, Aanaes K, Pressler T, Skov M, Ciofu O.

Diagnosis of biofilm infections in cystic fibrosis patients.

APMIS. 2017 Apr;125(4):339-343. doi: 10.1111/apm.12689. Review.

 

165. Kongstad TGreen KBuchvald FSkov MPressler TNielsen KG. Association between spirometry controlled chest CT scores using computer-animated biofeedback and clinical markers of lung disease in children with cystic fibrosis. Eur Clin Respir J. 2017 May 2;4(1):1318027. doi: 10.1080/20018525.2017.1318027. eCollection 2017.

 

166. Knudsen KB, Pressler T, Mortensen LH, Jarden M, Skov M, Quittner AL, Katzenstein T, Boisen KA.

Erratum to: Associations between adherence, depressive symptoms and health-related quality of life in young adults with cystic fibrosis.

Springerplus. 2017 May 31;5(1):2119. doi: 10.1186/s40064-017-3789-1. eCollection 2016.

 

167. Kongstad T, Green K, Buchvald F, Skov M, Pressler T, Nielsen KG.

Association between spirometry controlled chest CT scores using computer-animated biofeedback and clinical markers of lung disease in children with cystic fibrosis.

Eur Clin Respir J. 2017 May 2;4(1):1318027. doi: 10.1080/20018525.2017.1318027. eCollection 2017.

. doi: 10.1016/j.jhin.2017.04.020. Epub 2017 Apr 27.

 

168. Ratjen, F., C. Hug, G. Marigowda, S. Tian, X. Huang, S. Stanojevic, C. E. Milla, P. D. Robinson, D. Waltz and J. C. Davies (2017). "Efficacy and safety of lumacaftor and ivacaftor in patients aged 6-11 years with cystic fibrosis homozygous for F508del-CFTR: a randomised, placebo-controlled phase 3 trial." Lancet Respir Med. Jun 8. pii: S2213-2600(17)30215-1. doi: 10.1016/S2213-2600(17)30215-1. [Epub ahead of print]

 

169. Knudsen KB, Pressler T, Mortensen LH, Jarden M, Boisen KA, Skov M, Quittner AL, Katzenstein TL.

Coach to cope: feasibility of a life coaching program for young adults with cystic fibrosis.

Patient Prefer Adherence. 2017 Sep 21;11:1613-1623. doi: 10.2147/PPA.S141267. eCollection 2017.

           

170. Fernández-Barat L, Ciofu O, Kragh KN, Pressler T, Johansen U, Motos A, Torres A, Hoiby N. Phenotypic shift in Pseudomonas aeruginosa populations from cystic fibrosis lungs after 2-week antipseudomonal treatment. J Cyst Fibros. 2016 Sep 16. pii: S1569-1993(16)30601-4. doi: 10.1016/j.jcf.2016.08.005. [Epub ahead of print] PubMed PMID: 27651273.

           

171. Bregnballe V, Boisen KA, Schiotz PO, Pressler T, Lomborg K.

Flying the nest: a challenge for young adults with cystic fibrosis and their parents. Patient Prefer Adherence. 2017;11:229-36.

           

172. Ronit A, Mathiesen IH, Gelpi M, Benfield T, Gerstoft J, Pressler T, et al.

Small airway dysfunction in well-treated never-smoking HIV-infected individuals. Eur Respir J. 2017;49(3).

           

173. Schultz AN, Hoiby N, Nielsen XC, Pressler T, Dalhoff K, Duno M, et al.

Individual pharmacokinetic variation leads to underdosing of ciprofloxacin in some cystic fibrosis patients. Pediatr Pulmonol. 2017;52(3):319-23.


174. Hoiby, N., T. Bjarnsholt, C. Moser, P. O. Jensen, M. Kolpen, T. Qvist, K. Aanaes, T. Pressler, M. Skov and O. Ciofu (2017).

"Diagnosis of biofilm infections in cystic fibrosis patients." APMIS 125(4): 339-343.


175. Ronit, A., M. Gelpi, J. Argentiero, I. Mathiesen, S. D. Nielsen, T. Pressler and A. L. Quittner (2017). "Electronic applications for the CFQ-R scoring." Respir Res 18(1): 108.


2016

Buchvald F, Phillipsen LD, Hjuler T, Nielsen KG.
Pediatr Pulmonol. 2016 Nov;51(11):1200-1205. doi: 10.1002/ppul.23530.
PMID: 27717246 [PubMed - in process]
 
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Alanin MC, Aanaes K, Høiby N, Pressler T, Skov M, Nielsen KG, Johansen HK, von Buchwald C.
Int Forum Allergy Rhinol. 2016 Nov 23. doi: 10.1002/alr.21873. [Epub ahead of print]
PMID: 27879058 [PubMed - as supplied by publisher]
 
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Loomba RS, Danduran M, Nielsen KG, Ring AM, Kovach J, Anderson RH.
Pediatr Cardiol. 2016 Nov 23. [Epub ahead of print]
PMID: 27878633 [PubMed - as supplied by publisher]
 
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Ioan I, Demoulin-Alexikova S, Coutier L, Bonabel C, Kirkby J, Nielsen KG, Tomalak W, Thompson B, Schweitzer C, Robinson PD, Marchal F.
Eur Respir J. 2016 Dec;48(6):1804-1807. doi: 10.1183/13993003.01302-2016. No abstract available. 
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Kobbernagel HE, Buchvald FF, Haarman EG, Casaulta C, Collins SA, Hogg C, Kuehni CE, Lucas JS, Omran H, Quittner AL, Werner C, Nielsen KG.
BMC Pulm Med. 2016 Jul 22;16(1):104. doi: 10.1186/s12890-016-0261-x.
PMID: 27450411 [PubMed - in process] Free PMC Article 
 
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Sommer LM, Alanin MC, Marvig RL, Nielsen KG, Høiby N, von Buchwald C, Molin S, Johansen HK.
Sci Rep. 2016 Jun 28;6:28732. doi: 10.1038/srep28732.
PMID: 27349973 [PubMed - in process] Free PMC Article 
 
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Alanin MC, Aanaes K, Høiby N, Pressler T, Skov M, Nielsen KG, Taylor-Robinson D, Waldmann E, Krogh Johansen H, von Buchwald C.
Rhinology. 2016 Sep;54(3):206-13. doi: 10.4193/Rhin15.347.
PMID: 27116399 [PubMed - indexed for MEDLINE]
 
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Lochte L, Nielsen KG, Petersen PE, Platts-Mills TA.
BMC Pediatr. 2016 Apr 18;16:50. doi: 10.1186/s12887-016-0571-4. Review.
PMID: 27091126 [PubMed - indexed for MEDLINE] Free PMC Article 
 
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Sisman Y, Buchvald F, Blyme AK, Mortensen J, Nielsen KG.
Pediatr Pulmonol. 2016 Aug;51(8):830-7. doi: 10.1002/ppul.23360.
PMID: 26678017 [PubMed - in process]
 
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Werner C, Lablans M, Ataian M, Raidt J, Wallmeier J, Große-Onnebrink J, Kuehni CE, Haarman EG, Leigh MW, Quittner AL, Lucas JS, Hogg C, Witt M, Priftis KN, Yiallouros P, Nielsen KG, Santamaria F, Ückert F, Omran H.
Eur Respir J. 2016 Mar;47(3):849-59. doi: 10.1183/13993003.00776-2015.
PMID: 26659107 [PubMed - indexed for MEDLINE]
 
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Green K, Ejlertsen JS, Madsen A, Buchvald FF, Kongstad T, Kobbernagel H, Gustafsson PM, Nielsen KG.
Pediatr Pulmonol. 2016 Jun;51(6):624-32. doi: 10.1002/ppul.23339.
PMID: 26595237 [PubMed - in process]
 
Kristensen KH, Rytter MJ, Sørensen AC, Christensen VB, Namusoke H, Skov M, Andreassen BU, Friis H.
Ugeskr Laeger. 2016 Oct 3;178(40). pii: V03160185. Danish.

Knudsen KB, Pressler T, Mortensen LH, Jarden M, Skov M, Quittner AL, Katzenstein T, Boisen KA.
Springerplus. 2016 Jul 29;5(1):1216. doi: 10.1186/s40064-016-2862-5.

155. Lea M. Sommer, Rasmus L. Marvig, Adela Luján, Anna Koza, Tacjana Pressler, Søren Molin1, and Helle K. Johansen. Is genotyping of single isolates sufficient for population structure analysis of Pseudomonas aeruginosa in cystic fibrosis airways? BMC Genomics201617:589. DOI: 10.1186/s12864-016-2873-1

156. Knudsen KB, Pressler T, Mortensen LH, Jarden M, Skov M, Quittner AL, Katzenstein T, Boisen KA. Associations between adherence, depressive symptoms and health-related quality of life in young adults with cystic fibrosis. Springerplus. 2016 Jul 29;5(1):1216. doi: 10.1186/s40064-016-2862-5. PubMed PMID: 27516954; PubMed Central PMCID: PMC4967055.

157. Qvist T, Pressler T, Katzenstein TL, Høiby N, Collins MT. Evaluation of a bovine antibody test for diagnosing Mycobacterium avium complex in patients with cystic fibrosis. Pediatr Pulmonol. 2016 Sep 20. doi: 10.1002/ppul.23608. [Epub ahead of print] PubMed PMID: 27648735.

158. Fernández-Barat L, Ciofu O, Kragh KN, Pressler T, Johansen U, Motos A, Torres A, Hoiby N. Phenotypic shift in Pseudomonas aeruginosa populations from cystic fibrosis lungs after 2-week antipseudomonal treatment. J Cyst Fibros. 2016 Sep 16. pii: S1569-1993(16)30601-4. doi: 10.1016/j.jcf.2016.08.005. [Epub ahead of print] PubMed PMID: 27651273. 

159. Bryant JM, Grogono DM, Rodriguez-Rincon D, Everall I, Brown KP, Moreno P, Verma D, Hill E, Drijkoningen J, Gilligan P, Esther CR, Noone PG, Giddings O, Bell SC, Thomson R, Wainwright CE, Coulter C, Pandey S, Wood ME, Stockwell RE, Ramsay KA, Sherrard LJ, Kidd TJ, Jabbour N, Johnson GR, Knibbs LD, Morawska L, Sly PD, Jones A, Bilton D, Laurenson I, Ruddy M, Bourke S, Bowler IC, Chapman SJ, Clayton A, Cullen M, Dempsey O, Denton M, Desai M, Drew RJ, Edenborough F, Evans J, Folb J, Daniels T, Humphrey H, Isalska B, Jensen-Fangel S, Jönsson B, Jones AM, Katzenstein TL, Lillebaek T, MacGregor G, Mayell S, Millar M, Modha D, Nash EF, O'Brien C, O'Brien D, Ohri C, Pao CS, Peckham D, Perrin F, Perry A, Pressler T, Prtak L, Qvist T, Robb A, Rodgers H, Schaffer K, Shafi N, van Ingen J, Walshaw M, Watson D, West N, Whitehouse J, Haworth CS, Harris SR, Ordway D, Parkhill J, Floto RA. Emergence and spread of a human-transmissible multidrug-resistant nontuberculous mycobacterium. Science. 2016 Nov 11;354(6313):751-757. PubMed PMID: 27846606; PubMed Central PMCID: PMC5142603.


2015

136. Frommer A, Hjeij R, Loges NT, Edelbusch C, Jahnke C, Raidt J, Werner C, Wallmeier J, Große-Onnebrink J, Olbrich H, Cindrić S, Jaspers M, Boon M, Memari Y, Durbin R, Kolb-Kokocinski A, Sauer S, Marthin JK, Nielsen KG, Amirav I, Elias N, Eitan K, Shoseyov D, Haeffner K, Omran H.

Immunofluorescence Analysis and Diagnosis of Primary Ciliary Dyskinesia with Radial Spoke Defects.

Am J Respir Cell Mol Biol. 2015 Mar 19. [Epub ahead of print]


1
37. Hansen C, Skov M.

Evidence for the efficacy of aztreonam for inhalation solution in the management of Pseudomonas aeruginosa in patients with cystic fibrosis.

Ther Adv Respir Dis. 2015 Feb;9(1):16-21.


138. Mathias Munkholm, Kim Gjerum Nielsen & Jann Mortensen

Clinical value of measurement of pulmonary radioaerosol mucociliary clearance in the work up of primary ciliary dyskinesia

12/2015; 5(1):118. DOI:10.1186/s13550-015-0118-y​​


139. Paul D Robinson · Janet Stocks·Francois Marchal · Kim G Nielsen · Bruce R Thompson · Waldemar Tomalak · Jane Kirkby

Poor standardisation of plethysmographic specific airways resistance measurement despite widespread use.

European Respiratory Journal 08/2015; DOI:10.1183/13993003.00377-2015 · 7.13 Impact Factor ​


140. Heike Olbrich · Carolin Cremers · Niki T Loges · Claudius Werner · Kim G Nielsen · June K Marthin · Maria Philipsen · Julia Wallmeier · Petra Pennekamp · Tabea Menchen · Christine Edelbusch · Gerard W Dougherty · Oliver Schwartz · Holger Thiele · Janine Altmüller · Frank Rommelmann · Heymut Omran

Loss-of-Function GAS8 Mutations Cause Primary Ciliary Dyskinesia and Disrupt the Nexin-Dynein Regulatory Complex.

The American Journal of Human Genetics 09/2015; DOI:10.1016/j.ajhg.2015.08.012 · 10.93 Impact Factor
​​

141. Damgaard AL, Hansen BM, Mathiasen R, Buchvald F, Lange T, Greisen G.

Prematurity and prescription asthma medication from childhood to young adulthood: a Danish national cohort study.

PLoS One. 2015 Feb 4;10(2):e0117253. doi: 10.1371/journal.pone.0117253. eCollection 2015.


2014​

120. Skov M, Pressler T, Lykkesfeldt J, Poulsen HE, Jensen PØ, Johansen HK, Qvist T, Kræmer D, Høiby N, Ciofu O.

The effect of short-term, high-dose oral N-acetylcysteine treatment on oxidative stress markers in cystic fibrosis patients with chronic P. aeruginosa infection - A pilot study.

J Cyst Fibros. 2015 Mar;14(2):211-8. doi: 10.1016/j.jcf.2014.09.015. Epub 2014 Oct 23.

 

121. Qvist T, Gilljam M, Jönsson B, Taylor-Robinson D, Jensen-Fangel S, Wang M, Svahn A, Kötz K, Hansson L, Hollsing A, Hansen CR, Finstad PL, Pressler T, Høiby N, Katzenstein TL; Scandinavian Cystic Fibrosis Study Consortium (SCFSC).

Epidemiology of nontuberculous mycobacteria among patients with cystic fibrosis in Scandinavia.
J Cyst Fibros. 2015 Jan;14(1):46-52. doi: 10.1016/j.jcf.2014.08.002. Epub 2014 Aug 30.

 

122. Uhlving HH, Andersen CB, Christensen IJ, Gormsen M, Pedersen KD, Buchvald F, Heilmann C, Nielsen KG, Mortensen J, Moser C, Sengeløv H, Müller KG.

Biopsy-verified bronchiolitis obliterans and other noninfectious lung pathologies after allogeneic hematopoietic stem cell transplantation.

Biol Blood Marrow Transplant. 2015 Mar;21(3):531-8. doi: 10.1016/j.bbmt.2014.12.004. Epub 2014 Dec 9.

 

123. Alanin MC, Johansen HK, Aanaes K, Høiby N, Pressler T, Skov M, Nielsen KG, von Buchwald C.

Simultaneous sinus and lung infections in patients with primary ciliary dyskinesia.

Acta Otolaryngol. 2015 Jan;135(1):58-63. doi: 10.3109/00016489.2014.962185. Epub 2014 Nov 5.

 

124. Qvist T, Gilljam M, Jönsson B, Taylor-Robinson D, Jensen-Fangel S, Wang M, Svahn A, Kötz K, Hansson L, Hollsing A, Hansen CR, Finstad PL, Pressler T, Høiby N, Katzenstein TL;

Epidemiology of nontuberculous mycobacteria among patients with cystic fibrosis in Scandinavia.

Scandinavian Cystic Fibrosis Study Consortium (SCFSC).

J Cyst Fibros. 2015 Jan;14(1):46-52. doi: 10.1016/j.jcf.2014.08.002. Epub 2014 Aug 30.

 

125. Knudsen KB, Mathiesen ER, Eriksen V, Skov M, Nielsen KG, Johannesen J, Pressler T The development of diabetes among Danish cystic fibrosis patients over the last two decades.

Pediatr Diabetes. 2015 May;16(3):219-26. doi: 10.1111/pedi.12143. Epub 2014 Jun 1.

 

126. Joensen O, Paff T, Haarman EG, Skovgaard IM, Jensen PØ, Bjarnsholt T, Nielsen KG.

Exhaled breath analysis using electronic nose in cystic fibrosis and primary ciliary dyskinesia patients with chronic pulmonary infections.

PLoS One. 2014 Dec 26;9(12):e115584. doi: 10.1371/journal.pone.0115584. eCollection 2014.

 

127. Uhlving HH, Mathiesen S, Buchvald F, Green K, Heilmann C, Gustafsson P, Müller K, Nielsen KG.

Small airways dysfunction in long-term survivors of pediatric stem cell transplantation.

Pediatr Pulmonol. 2014 May 21. doi: 10.1002/ppul.23058. [Epub ahead of print]

 

128. Thomas A, Hanel B, Marott JL, Buchvald F, Mortensen J, Nielsen KG.

The single-breath diffusing capacity of CO and NO in healthy children of European descent.

PLoS One. 2014 Dec 16;9(12):e113177. doi: 10.1371/journal.pone.0113177. eCollection 2014.

 

129. Buchvald F, Nielsen KG.

 Diffuse lung disease in children.

Ugeskr Laeger. 2014 Aug 18;176(34). pii: V05130316. Danish.

 

130. Hjeij R, Onoufriadis A, Watson CM, Slagle CE, Klena NT, Dougherty GW, Kurkowiak M, Loges NT, Diggle CP, Morante NF, Gabriel GC, Lemke KL, Li Y, Pennekamp P, Menchen T, Konert F, Marthin JK, Mans DA, Letteboer SJ, Werner C, Burgoyne T, Westermann C, Rutman A, Carr IM, O'Callaghan C, Moya E, Chung EM; UK10K Consortium, Sheridan E, Nielsen KG, Roepman R, Bartscherer K, Burdine RD, Lo CW, Omran H, Mitchison HM.

CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formation.

Am J Hum Genet. 2014 Sep 4;95(3):257-74. doi: 10.1016/j.ajhg.2014.08.005.

 

131. Mathiesen S, Uhlving HH, Buchvald F, Hanel B, Nielsen KG, Müller K.

 Aerobic exercise capacity at long-term follow-up after paediatric allogeneic haematopoietic SCT.

Bone Marrow Transplant. 2014 Nov;49(11):1393-9. doi: 10.1038/bmt.2014.172. Epub 2014 Aug 11.

 

132. Maglione M, Bush A, Nielsen KG, Hogg C, Montella S, Marthin JK, Di Giorgio A, Santamaria F.

Multicenter analysis of body mass index, lung function, and sputum microbiology in primary ciliary dyskinesia.

Pediatr Pulmonol. 2014 Dec;49(12):1243-50. doi: 10.1002/ppul.22984. Epub 2014 Jan 13.

133. Mathiesen PR, Buchvald F, Nielsen KG, Herlin T, Friis T, Nielsen S.

Pulmonary function and autoantibodies in a long-term follow-up of juvenile dermatomyositis patients.

Rheumatology (Oxford). 2014 Apr;53 (4):644-9. doi: 10.1093/rheumatology/ket380. Epub 2013 Dec 5.​ 


134. Aanaes K, Eickhardt S, Johansen HK, von Buchwald C, Skov M, Høiby N, Bjarnsholt T.

Sinus biofilms in patients with cystic fibrosis: is adjusted eradication therapy needed?

Eur Arch Otorhinolaryngol. 2014 Oct 9. [Epub ahead of print]


135. Lewis AE, Høi-Hansen CE, Buchvald F, Petersen W.

Idiopathic pulmonary haemosiderosis in a one-year-old girl with Down syndrome.

Ugeskr Laeger. 2014 Sep 22;176(39). pii: V04140253. Danish.


2013​​​


101.Qvist T, Pressler T, Thomsen VO, Skov M, Iversen M, Katzenstein TL.
Nontuberculous Mycobacterial Disease Is Not a Contraindication to Lung Transplantation in Patients With Cystic Fibrosis: A Retrospective Analysis in a Danish Patient Population.
Transplant Proc.2013;45:342-5

102. Aanaes K, Johansen HK, Poulsen SS, Pressler T, Buchwald C, Høiby N.
"Secretory IgA as a diagnostic tool for Pseudomonas aeruginosa respiratory colonization."
J Cyst Fibros. 2013;12:81-87.

103.Christina Schjellerup Dalbøge, Tacjana Pressler, Niels Høiby, Kim Gjerum Nielsen, Helle Krogh Johansen
.A COHORT STUDY of the Copenhagen CF centre Eradication Strategy against Staphylococcus aureus in
 patients with CF.
J Cyst Fibros. 2013;12:42-8

104.Aanaes K, von Buchwald C, Hjuler T, Skov M, Alanin M, Johansen HK.
The effect of sinus surgery with intensive follow-up on pathogenic sinus bacteria in patients with cystic fibrosis.
Am J Rhinol Allergy. 2013 Jan;27(1):e1-4.

105. Yu D, Buchvald F, Brandt B, Nielsen KG.
Seventeen-year study shows rise in parapneumonic infections with higher treatment failure after chest tube drainage.
Acta Paediatr. 2013 Sep 30.

106. Christensen PM, Maltbæk N, Jørgensen IM, Nielsen KG.
Can flow-volume loops be used to diagnose exercise induced laryngeal obstructions? A comparison study examining the accuracy and inter-rater agreement of flow volume loops as a diagnostic tool.
Prim Care Respir J. 2013 Sep;22(3):306-11.

107. Aanaes K, Johansen HK, Skov M, Buchvald FF, Hjuler T, Pressler T, Hoiby N, Nielsen KG,
von Buchwald C.
Clinical effects of sinus surgery and adjuvant therapy in cystic fibrosis patients - can chronic
lung infections be postponed?
Rhinology. 2013 Sep;51(3):222-30.

108. Moore DJ, Onoufriadis A, Shoemark A, Simpson MA, Zur Lage PI, de Castro SC, Bartoloni L,
Gallone G, Petridi S, Woollard WJ, Antony D, Schmidts M, Didonna T, Makrythanasis P, Bevillard J,
Mongan NP, Djakow J, Pals G, Lucas JS, Marthin JK, Nielsen KG, Santoni F, Guipponi M, Hogg C,
Antonarakis SE, Emes RD, Chung EM, Greene ND, Blouin JL, Jarman AP, Mitchison HM
Mutations in ZMYND10, a Gene Essential for Proper Axonemal Assembly of Inner and Outer Dynein Arms in Humans and Flies, Cause Primary Ciliary Dyskinesia.
Am J Hum Genet. 2013 Aug 8;93(2):346-56.

109. Kobbernagel HE, Nielsen KG, Hanel B.
Hypoxic challenge test applied to healthy
children: influence of body positions and exertion
on pulse oximetric saturation.
Arch Dis Child. 2013 Aug;98(8):602-6.

110. Uhlving HH, Bang CL, Christensen IJ, Buchvald F, Nielsen KG, Heilmann CJ, Müller KG.
Lung function after allogeneic hematopoietic stem cell transplantation in children: a longitudinal study in a population-based cohort.
Biol Blood Marrow Transplant. 2013 Sep;19(9):1348-54.

111. Rosenfeld M, Allen J, Arets BH, Aurora P, Beydon N, Calogero C, Castile RG, Davis SD, Fuchs S, Gappa M, Gustaffson PM, Hall GL, Jones MH, Kirkby JC, Kraemer R, Lombardi E, Lum S, Mayer OH, Merkus P, Nielsen KG, Oliver C, Oostveen E, Ranganathan S, Ren CL, Robinson PD, Seddon PC, Sly PD, Sockrider MM, Sonnappa S, Stocks J, Subbarao P, Tepper RS, Vilozni D; American Thoracic Society Assembly on Pediatrics Working Group on Infant and Preschool Lung Function Testing.
An official American Thoracic Society workshop report: optimal lung function tests for monitoring cystic fibrosis, bronchopulmonary dysplasia, and recurrent wheezing in children less than 6 years of age.
Ann Am Thorac Soc. 2013 Apr;10(2):S1-S11.

112. Idorn L, Hanel B, Jensen AS, Juul K, Reimers JI, Nielsen KG, Søndergaard L.
New insights into the aspects of pulmonary diffusing capacity in Fontan patients.
Cardiol Young. 2013 Apr 3:1-9

113. Borgwardt L, Dali CI, Fogh J, Månsson JE, Olsen KJ, Beck HC, Nielsen KG, Nielsen LH, Olsen SO, Riise Stensland HM, Nilssen O, Wibrand F, Thuesen AM, Pearl T, Haugsted U, Saftig P, Blanz J, Jones SA, Tylki-Szymanska A, Guffon-Fouiloux N, Beck M, Lund AM.
Enzyme replacement therapy for alpha-mannosidosis: 12 months follow-up of a single centre, randomised, multiple dose study.
J Inherit Metab Dis. 2013 Nov;36(6):1015-24.

114. Marthin JK, Nielsen KG.
Hand-held tidal breathing nasal nitric oxide measurement--a promising targeted case-finding tool for the diagnosis of primary ciliary dyskinesia.
PLoS One. 2013;8(2):e57262.

115. Idorn L, Juul K, Jensen AS, Hanel B, Nielsen KG, Andersen H, Reimers JI, Sørensen KE, Søndergaard L.
Arrhythmia and exercise intolerance in Fontan patients: current status and future burden.
Int J Cardiol. 2013 Sep 30;168(2):1458-65.
 
116. Yu D, Buchvald F, Brandt B, Nielsen KG.
Seventeen-year study shows rise in parapneumonic infections with higher treatment failure after chest tube drainage.
Acta Paediatr. 2013 Sep 30.

117. Madsen A, Green K, Buchvald F, Hanel B, Nielsen KG.
Aerobic fitness in children and young adults with primary ciliary dyskinesia.
PLoS One. 2013 Aug 19;8(8):e71409.

118. Kongstad T, Buchvald FF, Green K, Lindblad A, Robinson TE, Nielsen KG.
Improved air trapping evaluation in chest computed tomography in children with cystic fibrosis using real-time spirometric monitoring and biofeedback.
J Cyst Fibros. 2013 Dec;12(6):559-66.

119. Pernille M. Christensen, John-Helge Heimdal, Kent L. Christopher, Caterina Bucca, Giovanna Cantarella, Gerhard Friedrich, Thomas Halvorsen, Felix Herth, Harald Jung, Michael J. Morris, Marc Remacle, Niels Rasmussen, and Janet A. Wilson.
ERS/ELS/ACCP 2013 international consensus conference nomenclature on inducible laryngeal obstructions.
Eur Respir Rev 2015; 24: 445–450


2012​

86. Uhlving HH, Buchvald F, Heilmann CJ, Kim Gjerum Nielsen,Gormsen M, Müller KG.
Bronchiolitis obliterans after allo-SCT: clinical criteria and treatment options.
Bone Marrow Transplant. 2012;47: 1020-9

87. Jacob Rasmussen, Kasper Aanæs, Rikke Norling, Kim Gjerum Nielsen, Helle Krogh Johansen, Christian von Buchwald.
CT of the paranasal sinuses is not a valid indicator for sinus surgery in CF patients.
J Cyst Fibros. 2012;11:93-9

88.Kongstad T, Buchvald F, Brenøe J, Petersen BL, Tabor A, Kim Gjerum Nielsen.
Radiology, histology and short-term outcome of asymptomatic congenital thoracic malformations.
Acta Paediatr. 2012;101:155-8.

89.Jacob Rasmussen, Aanæs K, Norling R, Kim Gjerum Nielsen, Johansen HK, von Buchwald C.
CT of the paranasal sinuses is not a valid indicator for sinus surgery in CF patients.
J Cyst Fibros. 2012;11:93-9.

90.Helle Krogh Johansen, Kasper Aanaes,
Tania Pressler, Kim Gjerum Nielsen,
Jacob Fisker,
Marianne Skov, Niels Høiby, Christian von Buchwald.
Colonisation and infection of the paranasal
sinuses in cystic fibrosis patients is
accompanied by a reduced PMN response.
J Cyst Fibros. 2012;11:525-31.

91.Heike Olbrich, Miriam Schmidts, Claudius Werner, Alexandros Onoufriadis, Niki T. Loges, Johanna Raidt,
Nora Fanni Banki, Amelia Shoemark, Tom Burgoyne, Saeed Al Turki, Matthew E. Hurles, UK10K, Gabriele Köhler, Josef Schroeder, Gudrun Nürnberg, Peter Nürnberg, Eddie M. K. Chung, Richard Reinhardt, June K. Marthin, Kim Gjerum Nielsen, Hannah M. Mitchison, and Heymut Omran.
Recessive HYDIN mutations cause Primary Ciliary Dyskinesia without randomization of left/right body asymmetry.
Am J Hum Genet. 2012;91:672-84.

92.Chawes BL, Jensen T, Olsen R, Joensen F, Nielsen KG, Buchvald F.
Plastic bronchitis in a ten year-old boy with Fontan circulation.
Ugeskr Laeger. 2012;174:1674-5.

93.Green K, Buchvald FF, Marthin JK, Hanel B, Gustafsson PM, Nielsen KG.
Ventilation inhomogeneity in children with primary ciliary dyskinesia.
Thorax. 2012;67:49-53.

94.Arendrup MC, Jensen RH, Grif K, Skov M, Pressler T, Johansen HK, Lass-FlörlC.
In vivo emergence of Aspergillus terreus with reduced azole susceptibility and a cyp51a M217I alteration.
J Infect Dis. 2012;206:981-5.

95.Johansen HK, Aanaes K, Pressler T, Nielsen KG, Fisker J, Skov M, Høiby N, von Buchwald C.
Colonisation and infection of the paranasal sinuses in cystic fibrosis patients is accompaniedby a reduced PMN response.
J Cyst Fibros. 2012;11:525-31.

96. Taylor-Robinson D, Whitehead M, Diderichsen F, Olesen HV, Pressler T, Smyth RL, Diggle P.
"Understanding the natural progression in %FEV1 decline in patients with cystic fibrosis:a longitudinal study."
Thorax. 2012 ;67:860-63

97.Assael BM, Pressler T, Bilton D, Fayon M, Fischer R, Chiron R, Larosa M, Knoop C, McElvaney N, Lewis SA, Bresnik M, Montgomery AB, Oermann CM; For the AZLI Active Comparator Study Group.
Inhaled aztreonamlysine vs. inhaled tobramycin in cystic fibrosis: A comparativeefficacy trial.
J Cyst Fibros. 2012 Sep 14.

98.Aanaes K, Rasmussen N, Pressler T, Segelmark M, Johansen HK, Lindberg U, Høiby N, Carlsson M, Wieslander J, von Buchwald C. 
Extensiveendoscopic image-guided sinus surgery decreases BPIANCA in patients with cystic fibrosis.
Scand J Immunol. 2012;76:573-9.

99.Maiken C. Arendrup, Rasmus H. Jensen, Katharina Grif, Marianne Skov, Tacjana Pressler, Helle K. Johansen, and Cornelia Lass-Flörl
In VivoEmergence of Aspergillus terreus with Reduced Azole Susceptibility anda 
Cyp51a M217I Alteration.
J Infect Dis. 2012; 15;206:981-5.

100.Döring G, Flume P, Heijerman H, Elborn JS; Consensus Study Group.
Treatment of lung infection in patients with cystic fibrosis: current and future strategies.
J Cyst Fibros. 2012;11:461-79​



2011


73. T. Pincikova, K. Nilsson, I. E. Moen, G. Fluge, A. Hollsing, P. K. Knudsen, A. Lindblad, L. Mared, T. Pressler, L. Hjelte..
Vitamin D deficiency as a risk factor for cystic fibrosis-related diabetes in the Scandinavian Cystic Fibrosis Nutritional Study.
Diabetologia. 2011.

74.Pincikova T, Nilsson K, Moen IE, Karpati F, Fluge G, Hollsing A, Knudsen PK, Lindblad A, Mared L, Pressler T, Hjelte L; Scandinavian Cystic Fibrosis Study Consortium.
Inverse relation between vitamin D and serum total immunoglobulin G in the Scandinavian Cystic Fibrosis Nutritional Study.
Eur J Clin Nutr. 2011;65:102-9.

75. Marthin JK, Kim Gjerum Nielsen.
Choice of Nasal Nitric Oxide Technique as first Line Test for Primary Ciliary Dyskinesia.
Eur Respir J. 2011 Mar;37(3):559-65.

76. Dalbøge CS, Hansen CR, Pressler T, Høiby N, Johansen HK.
Chronic pulmonary infection with Stenotrophomonas maltophilia and lung function in patients with cystic fibrosis.
J Cyst Fibros. 2011;10:318-25.

77. Pressler T, Bohmova C, Conway S, Dumcius S, Hjelte L, Høiby N, Kollberg H, Tümmler B, Vavrova V.
Chronic Pseudomonas aeruginosa infection definition: EuroCareCF Working Group report.
J Cyst Fibros. 2011;10 Suppl 2:S75-8.

78. Pressler, T.
Targeting Airway Inflammation in Cystic fibrosis in Children: Past, Present, and Future.
Pediatric Drugs:June 2011;13:141-7

79. Inger Elisabeth Moen, Kristina Nilsson, Anna Andersson, Morten Wang Fagerland, Gjermund Fluge, Annika Ericsson Hollsing, Marita Gilljam, Lena Mared, Tacjana Pressler, Henriette Santi, Olav-Trond Storrøsten, Lena Hjelte.
Dietary intake and nutritional status in a Scandinavian adult cystic fibrosis-population compared with recommendations.
Food & Nutrition Research 2011, 55

80. Mortensen KL, Jensen RH, Johansen HK, Skov M, Pressler T, Howard SJ, Leatherbarrow H, Mellado E, Arendrup MC.
Aspergillus species and other molds in respiratory samples from patients with cystic fibrosis: a laboratory-based study with focus on Aspergillus fumigatus azole resistance.
J Clin Microbiol. 2011;49:2243-51.

81. Aanaes K, Rickelt LF, Johansen HK, von Buchwald C, Pressler T, Høiby N, Jensen PØ.
Decreased mucosal oxygen tension in the maxillary sinuses in patients with cystic fibrosis.
J Cyst Fibros, 2011. 10: p. 114-20.

82. Becker-Heck A. Zohn IE, Okabe N, Pollck, Lanhart KB, Sullivan- Brown J, McSheen J, Loges NT, Olbrich H, Haeffner K, Fliegauf M, Horvarth J, Reinhardt B, Nielsen KG, Marthin JK, Baktai G, Anderson KV, Geisler B, Niswander L, Omran H, Burdine RD.
The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation.
Nature Genet. 2011;43:79-84.

83. Merveille AC, Davis EE, Becker-Heck A, Legendre M,Amirav I, Bataille G, Belmont J, beydon N, Billen F, Clement A, Clercx C, Coste A, Crosbie R, de Blic J, Deleuze S, Duquesnoy P, Escalier D, Escudier E, Fliegauf M, Horvath J, Hill K, Jorissen M, Just J, Kispert A, lathrop M, Loges NT, Marthin JK, Momozawa Y, Nielsen KG, Plbrich H, Papon JF, Rayet I,Roger G, Schmidts M, Tenreiro H, Towbin JA, Zelenika D, Zentgraf H, Georges M,
Lequarre AS, Katsanis N, Omran H, mselem S,. 
CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs.
Nature Genet. 2011;43:72-78.

84. Mette Siemsen, Niels E O Andersen, Kim Gjerum Nielsen.
EBUS in a 6 year old boy with enlarged hilar lymph nodes.
Journal of Bronchology and Interventional Pulmonology 2011,18:205.

85. Frederik Buchvald, LA Kristensen, Bodil Laub Petersen, Karen Damgaard, Robin Deterding, MD; Claire Langston, MD, Leland L Fan, MD; Gail H Deutsch, MD; Megan K Dishop, Kim Gjerum Nielsen.
Frequency, Treatment and Functional Outcome in Children with Hypersensitivity Pneumonitis.
Pediatr Pulmonol. 2011;46:1098-107.​



2010


63. Chawes BL, Buchvald F, Bischoff AL, Loland L, Hermansen M, Halkjaer LB, Bønnelykke K, Bisgaard H.
Elevated exhaled nitric oxide in high-risk neonates precedes transient early but not persistent wheeze.
Am J Respir Crit Care Med. 2010;182:138-42.

64. Rafiq S, Meldgaard CW, Buchvald F, Brandt B.
[Congenital aplasia of left-sided pericardium].
Ugeskr Laeger. 2010;172:547-8. Danish.

65. Raaschou-Nielsen O, Hermansen MN, Loland L, Buchvald F, Pipper CB, Sørensen M, Loft S, Bisgaard H.
Long-term exposure to indoor air pollution and wheezing symptoms in infants.
Indoor Air. 2010;20:159-67.

66. Hansen CR, Pressler T, Jensen PO, Bjarnsholt T, Høiby N.
Inflammation in Achromobacter xylosoxidans infected cystic fibrosis patients.
J Cyst Fibrosis. 2010;9:51-58.

67. Marthin JK, Petersen N, Skovgaard LT. Kim Gjerum Nielsen.
Lung Function in Patients with Primary Ciliary Dyskinesia. A Cross Sectional and Three-decade Longitudinal Study.
Am J Respir Crit Care Med.1;181:1262-8.

68. Kirkby J, Stanojevic S, Lum S, Bardier M, Beatdsmore C, Custovic A, Nielsen KG, Paton J, Tomalak W,Stocks J.
Reference equations for specific airway resistance in children: the asthma UK initiative.
Eur Respir J. 2010;36:622-9.

69. Kuehni CE, Frischer T, Strippoli MP, Maurer E, Bush A, Kim Gjerum Nielsen,  Escribano A, Lucas JS, Yiallouros P, Omran H, Eber E, O'Callaghan C, Snijders D, Barbato A;
For the ERS task force on primary ciliary dyskinesia in children. Factors influencing age at diagnosis of primary ciliary dyskinesia in European children.
Eur Respir J. 2010, 36:1248-58.

70. Nørskov-Lauritsen N, Johansen HK, Fenger MG, Nielsen XC, Pressler T, Olesen HV, Høiby N. H.K. Johansen, M.G. Fenger, 
Unusual Distribution of Burkholderia cepacia Complex Species in Danish Cystic Fibrosis Clinics May Stem from Restricted transmission between Patients.
J Clin Microbiol, 2010;48:2981-3.

71. Andersen JB, Mortensen J, Damgaard K, Skov M, Sparup J, Petersen BL, Rechnitzer C, Borgwardt L.
Fourteen-year-old girl with endobronchial carcinoid tumour presenting with asthma and lobar emphysema.
Clin Respir j. 2010, 4:120-4.

72. Olesen HV, Pressler T, Hjelte L, Mared L, Lindblad A, Knudsen PK, Laerum BN, Johannesson M;
Gender differences in the Scandinavian cystic fibrosis population.
Pediatr Pulmonol. 2010: 45: pp 959-965.​


2009

55. Kolpen M, Hansen CR, Bjarnsholt T, Moser C, Christensen LD, van Gennip M, Ciofu O, Mandsberg L,
Kharazmi A, Döring G, Givskov M, Høiby N, Jensen PØ.
Polymorphonuclear leucocytes consume oxygen in sputum from chronic Pseudomonas aeruginosa pneumonia in cystic fibrosis.
Thorax, 2009. 65: p. 57-62.

56. Knudsen PK, Olesen HV, Høiby N, Johannesson M, Karpati F, Laerum BN, Meyer P, Pressler T, Lindblad A; Scandinavian CF Study Consortium (SCFSC). 
Differences in prevalence and treatment of Pseudomonas aeruginosa in cystic fibrosis centres in Denmark, Norway and Sweden.
J Cyst Fibros, 2009. 8.135-42

57. Pressler T, Karpati F, Granström M, Knudsen PK, Lindblad A, Hjelte L, Olesen HV, Meyer P, Høiby N;
Scandinavian CF Study Consortium.
Diagnostic significance of measurements of specific IgG antibodies to Pseudomonas aeruginosa by three different serological methods.
Journal of cystic fibrosis. 2009. 8: 37-42.

58. Hansen CR, Pressler T, Hoiby N, Johansen HK.
Long-term, low-dose azithromycin treatment reduces the incidence but increases macrolide resistance in Staphylococcus aureus in Danish CF patients.
Journal of cystic fibrosis. 2009. 8: 58-62.

59. Fluge G, Olesen HV, Gilljam M, Meyer P, Pressler T, Storrösten OT, Karpati F, Hjelte L.
Co-morbidity of cystic fibrosis and celiac disease in Scandinavian cystic fibrosis patients.
J Cyst Fibros., 2009. 8: p. 198-202.

60. Bjarnsholt T, Jensen PØ, Fiandaca MJ, Pedersen J, Hansen CR, Andersen CB, Pressler T, Givskov M, Høiby N.
Pseudomonas aeruginosa biofilms in the respiratory tract of cystic fibrosis patients.
Pediatr Pulmonol., 2009. 44: p. 547-58.

61. Heijerman H, Westerman E, Conway S, Touw D, Döring G; consensus working group.
Inhaled medication and inhalation devices for lung disease in patients with cystic fibrosis: A European consensus.
J Cyst Fibros., 2009. 8: p. 295-315.

62. Barbato A., T. Frischer, C. E. Kuehni, D. Snijders, I. Azevedo, G. Baktai, L. Bartoloni, E. Eber, A. Escribano, E. Haarman, B. Hesselmar, C. Hogg, M. Jorissen, J. Lucas, Kim Gjerum Nielsen, C. O'Callaghan, H. Omran, P. Pohunek, M-P. F. Strippoli, and A. Bush.
Primary ciliary dyskinesia: a consensus statement on diagnostic and treatment approaches in children.
Eur Respir J 2009;34 1264-1276.



2008


51. Birgitte Boysen Kjaer, Jorgen Skov Jensen, Kim Gjerum Nielsen, Anders Fomsgaard, Blenda Böttiger, Birthe Dohn, and Hans Bisgaard. 
Lung function and bronchial responsiveness after Mycoplasma pneumonie infection in early childhood.
Pediatr Pulmonol. 2008;43:567-75.

52. Johansen HK, Moskowitz SM, Ciofu O, Pressler T, Høiby N.,
Spread of colistin resistant non-mucoid Pseudomonas aeruginosa among chronically infected Danish cystic fibrosis patients.
J Cyst Fibros., 2008. 7: 391-7.

53. Hansen, C.R., T. Pressler, and N. Hoiby,
Early aggressive eradication therapy for intermittent Pseudomonas aeruginosa airway colonization in cystic fibrosis patients: 15 years experience.
J Cyst Fibros., 2008. 7: 523-30.

54. Pressler, T.,
Review of recombinant human deoxyribonuclease (rhDNase) in the management of patients with cystic fibrosis.
Biologics: Targets & Therapy, 2008. 2. 611-7.



2007


47. Carlsson M., Eriksson L., Pressler T., Kornfalt R., Mared L., Meyer P., et al.,
Autoantibody response to BPI predict disease severity and outcome in cystic fibrosis.
J Cyst Fibros. 2007, 6: 228-33.

48. Jensen P.O., Bjarnsholt T., Phipps R., Rasmussen T.B., Calum H., Christoffersen L, et al.,
Rapid necrotic killing of polymorphonuclear leukocytes is caused by quorum-sensingcontrolled production of rhamnolipid by Pseudomonas aeruginosa.
Microbiology. 2007, 153: 1329-38.

49. June K. Marthin, Jann Mortensen, Tacjana Pressler, Kim Gjerum Nielsen.
Pulmonary Radioaerosol Mucociliary Clearance in Diagnosis of Primary Ciliary Dyskinesia.
Chest.2007; 132: 966-976.

50. Bisgaard H, Hermansen MN, Buchvald F, Loland L, Halkjaer LB, Bønnelykke K, Brasholt M, Heltberg A, Vissing NH, Thorsen SV, Stage M, Pipper CB.
Childhood asthma after bacterial colonization of the airway in neonates.
N Engl J Med. 2007;357:1487-95.



2006​


36. Halkjaer LB, Loland L, Buchvald FF, Agner T, Skov L, Strand M, Bisgaard H.
Development of atopic dermatitis during the first 3 years of life: the Copenhagen prospective study on asthma in childhood cohort study in high-risk children.
Arch Dermatol. 2006;142:561-6.

37. Bisgaard H, Hermansen MN, Loland L, Halkjaer LB, Buchvald F.
Intermittent inhaled corticosteroids in infants with episodic wheezing.
N Engl J Med. 2006 11;354:1998-2005.

38. Loland L, Buchvald FF, Halkjaer LB, Anhøj J, Hall GL, Persson T, Krause TG, Bisgaard H.
Sensitivity of bronchial responsiveness measurements in young infants.
Chest. 2006;129:669-75.

39. Kim Gjerum Nielsen.
Lung function and bronchial responsiveness in young children.
Thesis in Dan Med Bull.2006; 53: 46-75.

40. Mette Hermansen, Kim Gjerum Nielsen, Frederik Buchvald, Jakob Jessing Jespersen, Thomas Bengtsson, Hans Bisgaard.
Acute Relief of Exercise-Induced Bronchoconstriction by Inhaled Formoterol in Children With Persistent Asthma.
Chest 2006; 129:1203–1209.

41. Kim Gjerum Nielsen. P
Plethysmographic specific airway resistance.
Paediatr Respir Rev. 2006; 7: suppl 1: 17-19.

42. Kim Gjerum Nielsen.
Forced oscillation technique.
Paediatr Respir Rev. 2006; 7: suppl 1: 8-10.

43. Pressler T., Frederiksen B., Skov M., Garred P., Koch C., Høiby N.
Early rise of anti-pseudomonas antibodies and a mucoid phenotype of Pseudomonas aeruginosa are risk factors for development of chronic lung infection. A case control study.
J Cyst Fibros. 2006, 5: 9-15.

44. Rønne Hansen C., Pressler T., Høiby N., Gormsen M.
Chronic infection with Achromobacter xylosoxidans in cystic fibrosis patients; a retrospective case control study.
J Cyst Fibros. 2006,5: 245-51.

45. Frederiksen B., Pressler T., Hansen A., Koch C., Høiby N.
Effect of aerosolized rhDNase (Pulmozyme) on pulmonary colonization in patients with cystic fibrosis.
Acta Paediatr. 2006, 95: 1070-4.

46. Andersen H.U., Lanng S., Pressler T., Laugesen C.S., Mathiesen E.R.
Cystic fibrosisrelated diabetes: the presence of microvascular diabetes complications.
Diabetes Care. 2006, 29: 2660-3.



2005

24. Bundgaard H, Skov M.
Hypokaleamia-induced arrhytmia – the assassin in beta-2 agonist treated patients?
Letter in BMJ 2005.

25. Skov M, McKay K, Koch C, Cooper PJ.
Prevalence of allergic broncho-pulmonary aspergillosis in cystic fibrosis in an area with a high frequency of atopy.
Resp Medicine 2005; 99: 887-893.

26. Oana Ciofu, Bente Riis, Tacjana Pressler, Henrik Enghusen Poulsen and Niels Høiby.
Occurrence of Hypermutable Pseudomonas aeruginosa in Cystic Fibrosis Patients is associated with the Oxidative Stress Caused by Chronic Lung Inflammation.
Antimicrobial Agents and Chemotherapy. 2005, 49: 2276-2282.

27. Christopher M. Burton, Tacjana Pressler, Nils Milman.
Pulmonary sarcoidosis in a Child with Cystic Fibrosis. Pediatric pulmonology.
Pediatr Pulmonol. 2005, 39: 473-7.

28. Christine Rønne Hansen, Tacjana Pressler, Christian Koch and Niels Høiby.
Longterm Azitromycin treatment of cystic fibrosis patients with chronic P. aeruginosa infection.
J Cyst Fibros. 2005, 4: 35-40.

29. Moser, C. Jensen P.O., Pressler T., Frederiksen B., Lanng S., Kharazmi A., Koch C., Høiby N.
Serum concentrations of GM-CSF and G-CSF correlate with the Th1/Th2 cytokine response in cystic fibrosis patients with chronic Pseudomonas aeruginosa lung infection.
Apmis, 2005. 113: p. 400-9.

30. Høiby N., Frederiksen B., Pressler T., et al.,
Eradication of earlyPseudomonas aeruginosa infection in cystic fibrosis patients with chronic Pseudomonas aeruginosa lung infection.
J Cyst Fibros, 2005. 4 (Suppl 2): p. 49-54.

31. Kim Gjerum Nielsen, H Bisgaard.
Hyperventilation with Cold versus Dry Air in 2 – to 5 –year-old Children with Asthma.
Am J Respir Crit Care Med 2005; 171: 238-241.

32. Hans Bisgaard, Kim Gjerum Nielsen. P
Plethysmographic Measurements of Specific Airway Resistance in Young Children.
Chest 2005; 128: 355-362.

33. Frederik Buchvald, Mette Hermansen, Kim Gjerum Nielsen, Hans Bisgaard.
Exhaled Nitric Oxide Predicts Exercise Induced Bronchoconstriction in Asthmatic School Children.
Chest 2005; 128:1964–1967.

34. Kim Gjerum Nielsen, Bisgaard H.
Cold air challenge and specific airway resistance in preschool children.
Paediatr Respir Rev. 2005;6:255-66.

35. Buchvald F, Baraldi E, Carraro S, Gaston B, De Jongste J,Pijnenburg MW, Silkoff PE, Bisgaard H.
Measurements of exhaled nitric oxide in healthy subjects age 4 to 17 years.
 J Allergy Clin Immunol. 2005;115:1130-6.​



2004

17. D Jeganathan, R Chodhari, M Meeks, O Færoe, D Smyth, Kim Gjerum Nielsen, A S. Luder, I Amirav, H Bisgaard, R M Gardiner, E M K Chung, H M Mitchison.
Loci for primary ciliary dyskinesia map to chromosome 16p12.1-12.2 and 15q13.1-15.1 in Faroe Islands and Israeli Druze genetic isolates.
J Med Genet 2004; 41:233-240.

18. Kim Gjerum Nielsen, T Pressler, B Klug, C Koch, H Bisgaard.
Serial Lung Function and Responsiveness in Cystic Fibrosis during Early Childhood.
Am J Respir Crit Care Med 2004; 169: 1209-1216.

19. Johansen H.K., Norregaard L., Gotzsche P.C., Pressler T., Koch C., Høiby N.
Antibody response to Pseudomonas aeruginosa in cystic fibrosis patients: A marker of therapeutic success? A 30-year Cohort study of survival in Danish CF patients after onset of chronic P. aeruginosa lung infection.
Pediatr Pulmonol. 2004, 37: 427-32.

20. Bo Bech, Tanja Pressler, Martin Iversen, Jørn Carlsen, Nils Milman, Kirsten Eliasen, Mario Perko, Henrik Arendrup.
Long-term outcome of lung transplantation for cystic fibrosis – Danish results.
European Journal of cardio-thoracic surgery. 26: 1180-1186.

21. Döring G., Høiby N. Consensus Study Group.
Early intervention and prevention of lung disease in cystic fibrosis: A European consensus.
J Cyst Fibros. 2004, 3: 67-91.

22. Skov M, Pandey JP, Pressler T, Høiby N, Koch C.
Immunoglobulin allotypes and IgG subclass antibody response to Aspergillus fumigatus in cystic fibrosis patients.
J Cystic Fibrosis 3, 2004; 173-178.

23. Skov M, McKay K, Koch C, Cooper P.J.
Prevalence of allergic broncho-pulmonary aspergillosis in cystic fibrosis in an area with a high frequency of atopy.
J of Cyst Fibr 2004; 3: 173-178.



2003

11. Skov M, Main KM, Sillesen IB, Müller JR, Koch C, Thorsteinsson SL.
Binyrebarkinsufficiens efter kombineret behandling med itraconazol og budesonid.
Ugeskrift for Læger 2003;154 : 2198-202.

12. Stevens DA, Moss R, Kurup VP, Knutsen AP, Greenberger P,
Judson MA, Denning DW, Crameri R, Brody A, Light M, Skov M,
Maish W, Mastella G and the Cystic Fibrosis Foundation Consensus Conference.
Allergic bronchopulmonary aspergillosis in cystic  fibrosis – State of the Art: Cystic Fibrosis Foundation Consensus Conference.
Clin Infect Dis 2003; 37, Suppl 3: S225-64.

13. Jorgensen I.M., Johansen H.K., Frederiksen B., Pressler T., Hansen A.,
Vandamme P., Høiby N., Koch C. 
Epidemic spread of Pandoraea apista, a new pathogen causing severe lung disease in cystic fibrosis patients.
Pediatr Pulmonol. 2003; 36: 439-46.

14. Buchvald F, Eiberg H, Bisgaard H.
Heterogeneity of FeNO response to inhaled steroid in asthmatic children.
Clin Exp Allergy. 2003;33:1735-40.

15. Buchvald F, Bisgaard H. C
Comparisons of the complementary effect on exhaled nitric oxide of salmeterol vs montelukast in asthmatic children taking regular inhaled budesonide.
Ann Allergy Asthma Immunol. 2003;91:309-13.

16. H Bisgaard, M Hermansen, C Vrang, EA Andersen, G Dybmose, V Brændholt, K.G. Nielsen, E. Fog, L.V Pedersen, B. Smidth, B. Klug, J. Henriksen, M. Jørgensen, K Bønnelykke, D. Skoner, D Gentile.
A Randomized Trial of Montelukast in Respiratory Syncytial Virus Post-Bronchiolitis.
Am J Respir Crit Care Med 2003; 167:379–383.​



2002

5. Kristensen K, Andersen EA, Andersen MH, Buchvald FF, Christensen H,
Heslet L, Bunk Lauritsen TL, Reveles RM, Sorgenfrei IF, Winther-Rasmussen S.
A three year population based survey of paediatric mechanical ventilation in east Denmark.
Dan Med Bull. 2002;49:67-9.

6. Garred P, Pressler T, Lanng S, Madsen HO, Moser C, Laursen I, Balstrup F,
Koch C, Koch C. 
Mannose-binding lectin (MBL) therapy in an  MBL-deficient patient with severe cystic fibrosis lung disease.
Pediatr Pulmonol. 2002 ;33:201-7.

7. Main KM, Skov M, Sillesen IB, Dige-Petersen H, Müller J, Koch C, Lanng S.
Cushing's syndrome due to pharmacological interaction in a cystic fibrosis patient.
Acta Paediatr. 2002;91:1008-11.

8. Skov M, Main KM, Sillesen IB, Müller J, Koch C, Lanng S.
Iatrogenic adrenal insufficiency as a side-effect of combined treatment of itraconazole and budesonide.
Eur Respir J. 2002 20:127-33.

9. Skov M, Høiby N, Koch C.
Itraconazole treatment of allergic bronchopulmonary aspergillosis in patients with cystic fibrosis.
Allergy. 2002 ;57:723-8.

10. Main KM, Skov M, Sillesen IB, Dige-Petersen H,
Lanng S, Müller J, Koch C.
Iatrogen Cushing´s syndrome in a cystic fibrosis patient due to the interaction between budesonide and itraconazole.
Acta Pæd. 2002; 91: 1008-11.​



2001

1.Kim Gjerum Nielsen, H. Bisgaard.
Bronchodilation and bronchoprotection on asthmatic preschool children from formoterol administered by mechanically actuated dr​y-powder inhaler and spacer.
Am J Respir Crit Care Med 2001; 164: 256-259.

2. Kim Gjerum Nielsen, H. Bisgaard.
Discriminative capacity of bronchodilator response measured with three different lung function techniques in asthmatic and healthy children aged 2 to 5 years.
Am J Respir Crit Care Med 2001; 164: 554-559.

3. Anja Poulsen, Ann Kathrin Demeny,
Charlotte Bang Plum, Kim Gjerum Nielsen,
Kjeld Schmiegelow.
Pneumocystis Carinii pneumonia during maintenance treatment of childhood
acute lymphoblastic leukemia.
Med. Pediatr. Oncol. 2001;37:20-23.

4. Buchvald F, Bisgaard H.
FeNO measured at fixed exhalation flow rate during controlled tdal breathing in children from the age of 2 yr.
Am J Respir Crit Care Med. 2001, 699-704.​
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