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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Detalles Bibliográficos
Autores principales: Ardura-Garcia, Cristina, Goutaki, Myrofora, Carr, Siobhán B., Crowley, Suzanne, Halbeisen, Florian S., Nielsen, Kim G., Pennekamp, Petra, Raidt, Johanna, Thouvenin, Guillaume, Yiallouros, Panayiotis K., Omran, Heymut, Kuehni, Claudia E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2020
Materias:
Reviews
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7248350/
https://www.ncbi.nlm.nih.gov/pubmed/32494577
http://dx.doi.org/10.1183/23120541.00005-2020

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7248350/
https://www.ncbi.nlm.nih.gov/pubmed/32494577
http://dx.doi.org/10.1183/23120541.00005-2020

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