Registries and collaborative studies for primary ciliary dyskinesia in Europe

Registries and collaborative studies for primary ciliary dyskinesia in Europe

Primary ciliary dyskinesia (PCD) is a rare inherited disease characterised by malfunctioning cilia leading to a heterogeneous clinical phenotype with many organ systems affected. There is a lack of data on clinical presentation, prognosis and effectiveness of treatments, making it mandatory to impro...

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Bibliographic Details
Main Authors: Cristina Ardura-Garcia, Myrofora Goutaki, Siobhán B. Carr, Suzanne Crowley, Florian S. Halbeisen, Kim G. Nielsen, Petra Pennekamp, Johanna Raidt, Guillaume Thouvenin, Panayiotis K. Yiallouros, Heymut Omran, Claudia E. Kuehni
Format: Article
Language:English
Published: European Respiratory Society 2020-05-01
Series:ERJ Open Research
Online Access:http://openres.ersjournals.com/content/6/2/00005-2020.full

Internet

http://openres.ersjournals.com/content/6/2/00005-2020.full

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