Diagnosis, monitoring, and treatment of primary ciliary dyskinesia: PCD foundation consensus recommendations based on state of the art review

Primary ciliary dyskinesia (PCD) is a genetically heterogeneous, rare lung disease resulting in chronic oto‐sino‐pulmonary disease in both children and adults. Many physicians incorrectly diagnose PCD or eliminate PCD from their differential diagnosis due to inexperience with diagnostic testing meth...

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Detalhes bibliográficos
Publicado no:Pediatr Pulmonol
Main Authors: Shapiro, Adam J., Zariwala, Maimoona A., Ferkol, Thomas, Davis, Stephanie D., Sagel, Scott D., Dell, Sharon D., Rosenfeld, Margaret, Olivier, Kenneth N., Milla, Carlos, Daniel, Sam J., Kimple, Adam J., Manion, Michele, Knowles, Michael R., Leigh, Margaret W.
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2015
Assuntos:
State of the Art
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4912005/
https://ncbi.nlm.nih.gov/pubmed/26418604
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ppul.23304
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