The international primary ciliary dyskinesia cohort (iPCD Cohort): methods and first results
Myrofora Goutaki, Elisabeth Maurer, Florian S. Halbeisen, Israel Amirav, Angelo Barbato, Laura Behan, Mieke Boon, Carmen Casaulta, Annick Clement, Suzanne Crowley, Eric Haarman, Claire Hogg, Bulent Karadag, Cordula Koerner-Rettberg, Margaret W. Leigh, Michael R. Loebinger, Henryk Mazurek, Lucy Morgan, Kim G. Nielsen, Heymut Omran, Nicolaus Schwerk, Sergio Scigliano, Claudius Werner, Panayiotis Yiallouros, Zorica Zivkovic, Jane S. Lucas, Claudia E.Kuehni, on behalf of the PCD Italian Consortium, on behalf of the Swiss PCD Group, on behalf of the French Reference Centre for Rare Lung Diseases, on behalf of the Genetic Disorders of Mucociliary Clearance Consortium
Source: Eur Respir J 2017; 49(1): 1601181; DOI: 10.1183/13993003.01181-2016
Disease area: Paediatric lung diseases
Rating:
You must login to grade this presentation.
Share or cite this content
Citations should be made in the following way:
Myrofora Goutaki, Elisabeth Maurer, Florian S. Halbeisen, Israel Amirav, Angelo Barbato, Laura Behan, Mieke Boon, Carmen Casaulta, Annick Clement, Suzanne Crowley, Eric Haarman, Claire Hogg, Bulent Karadag, Cordula Koerner-Rettberg, Margaret W. Leigh, Michael R. Loebinger, Henryk Mazurek, Lucy Morgan, Kim G. Nielsen, Heymut Omran, Nicolaus Schwerk, Sergio Scigliano, Claudius Werner, Panayiotis Yiallouros, Zorica Zivkovic, Jane S. Lucas, Claudia E.Kuehni, on behalf of the PCD Italian Consortium, on behalf of the Swiss PCD Group, on behalf of the French Reference Centre for Rare Lung Diseases, on behalf of the Genetic Disorders of Mucociliary Clearance Consortium. The international primary ciliary dyskinesia cohort (iPCD Cohort): methods and first results. Eur Respir J 2017; 49(1): 1601181; DOI: 10.1183/13993003.01181-2016
You must login to share this Presentation/Article on Twitter, Facebook, LinkedIn or by email.
Member's Comments
Related content which might interest you:
Related content which might interest you:
Lung function in patients with primary ciliary dyskinesia: an iPCD Cohort study Source: Eur Respir J, 52 (2) 1801040; 10.1183/13993003.01040-2018 Year: 2018
The international primary ciliary dyskinesia (PCD) registry reports genotype/phenotype-correlations Source: Virtual Congress 2021 – Comorbidities in airway obstructive diseases Year: 2021
An international registry for primary ciliary dyskinesia Source: Eur Respir J 2016; 47: 849-859 Year: 2016
Registries and collaborative studies for primary ciliary dyskinesia in Europe Source: ERJ Open Res, 6 (2) 00005-2020; 10.1183/23120541.00005-2020 Year: 2020
Diagnosis of primary ciliary dyskinesia in a Dutch cohort of 63 pediatric patients: An overview Source: Annual Congress 2011 - Innate and exogenous factors in childhood respiratory infection Year: 2011
The nation-wide survey of primary ciliary dyskinesia in Japan Source: International Congress 2018 – Airway disease: recent discoveries Year: 2018
Primary ciliary dyskinesia: phenotypic features of a cohort of patients in Argentina Source: Annual Congress 2008 - Paediatric respiratory epidemiology I: primary ciliary dyskinesia, sleep-disordered breathing, exercise-induced symptoms and rare diseases Year: 2008
Clinical features & management of 334 children with primary ciliary dyskinesia in the English National Cohort Source: International Congress 2018 – Primary ciliary dyskinesia and lung function tests in respiratory morbidities Year: 2018
The Palestinian primary ciliary dyskinesia (PCD) cohort: clinical, diagnostic and genetic spectrum Source: Virtual Congress 2021 – Causes and consequences of paediatric respiratory diseases Year: 2021
The French national cohort of children with primary ciliary dyskinesia Source: International Congress 2014 – Paediatric epidemiology: new insights into primary ciliary dyskinesia, prematurity and bronchiolitis Year: 2014
Service delivery models for primary ciliary dyskinesia, an international comparison Source: Virtual Congress 2021 – Primary ciliary dyskinesia and tracheostomy Year: 2021
Standardised clinical data from patients with primary ciliary dyskinesia: FOLLOW-PCD Source: ERJ Open Res, 6 (1) 00237-2019; 10.1183/23120541.00237-2019 Year: 2020
Characteristics and outcomes of adults with primary ciliary dyskinesia (PCD): an EMBARC/BEAT-PCD analysis Source: Virtual Congress 2021 – Bronchiectasis Year: 2021
The time is right for an international primary ciliary dyskinesia disease registry Source: Eur Respir J 2017; 49(1): 1602143; DOI: 10.1183/13993003.02143-2016 Year: 2017
A longitudinal study characterising a large adult primary ciliary dyskinesia population Source: Eur Respir J 2016; 48: 441-450 Year: 2016
Primary ciliary dyskinesia (PCD): european survey on diagnostic and therapeutic practices Source: Eur Respir J 2007; 30: Suppl. 51, 403s Year: 2007
Preliminary results of high-speed video-microscopy and immunofluorescence analysis in a Spanish cohort of patients with primary ciliary dyskinesia Source: International Congress 2019 – A mixture of rare lung diseases Year: 2019
Retrospective study of lung function in a group of patients with primary ciliary dyskinesia Source: Eur Respir J 2001; 18: Suppl. 33, 296s Year: 2001
Longitudinal microbiology of children with primary ciliary dyskinesia Source: Annual Congress 2012 - New insights into respiratory infections in children Year: 2012
Primary ciliary dyskinesia in adults with bronchiectasis: Data from the Embarc registry Source: International Congress 2018 – The global impact of bronchiectasis and nontuberculous mycobacteria (NTM) Year: 2018