The Swiss Primary Ciliary Dyskinesia registry: objectives, methods and first results

Primary ciliary dyskinesia (PCD) is a rare, hereditary, multiorgan disease caused by defects in the structure and function of motile cilia. It results in a wide range of clinical manifestations, most commonly in the upper and lower airways. Central data collection in national and international reg...

Descripció completa

Dades bibliogràfiques

Autors principals:	Myrofora Goutaki, Marc O. Eich, Florian S. Halbeisen, Juerg Barben, Carmen Casaulta, Christian Clarenbach, Gaudenz Hafen, Philipp Latzin, Nicolas Regamey, Romain Lazor, Stefan Tschanz, Maura Zanolari, Elisabeth Maurer, Claudia E. Kuehni, for the Swiss PCD Registry (CH-PCD) Working Group
Format:	Artigo
Idioma:	Inglês
Publicat:	SMW supporting association (Trägerverein Swiss Medical Weekly SMW) 2019-01-01
Col·lecció:	Swiss Medical Weekly
Matèries:	Epidemiology orphan diseases patient registry primary ciliary dyskinesia Swiss Primary Ciliary Dyskinesia Registry
Accés en línia:	https://www.smw.ch/index.php/smw/article/view/2562
Etiquetes:	Afegir etiqueta Sense etiquetes, Sigues el primer a etiquetar aquest registre!