Primary ciliary dyskinesia in Japan: systematic review and meta-analysis

BACKGROUND: Primary ciliary dyskinesia (PCD) is a rare genetic disorder. Although the genetic tests and new diagnostic algorithms have recently been recommended, clinical signs and electron microscope (EM) findings have historically been the mainstays of diagnosis in Asia. To characterize PCD previo...

Descripción completa

Detalles Bibliográficos
Autores principales: Inaba, Atsushi, Furuhata, Masanori, Morimoto, Kozo, Rahman, Mahbubur, Takahashi, Osamu, Hijikata, Minako, Knowles, Michael R., Keicho, Naoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6659197/
https://www.ncbi.nlm.nih.gov/pubmed/31345208
http://dx.doi.org/10.1186/s12890-019-0897-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6659197/
https://www.ncbi.nlm.nih.gov/pubmed/31345208
http://dx.doi.org/10.1186/s12890-019-0897-4

Ejemplares similares