Clinical Features and Associated Likelihood of Primary Ciliary Dyskinesia in Children and Adolescents

Rationale: Primary ciliary dyskinesia (PCD), a genetically heterogeneous, recessive disorder of motile cilia, is associated with distinct clinical features. Diagnostic tests, including ultrastructural analysis of cilia, nasal nitric oxide measurements, and molecular testing for mutations in PCD gene...

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Detalhes bibliográficos
Publicado no:Ann Am Thorac Soc
Main Authors: Leigh, Margaret W., Ferkol, Thomas W., Davis, Stephanie D., Lee, Hye-Seung, Rosenfeld, Margaret, Dell, Sharon D., Sagel, Scott D., Milla, Carlos, Olivier, Kenneth N., Sullivan, Kelli M., Zariwala, Maimoona A., Pittman, Jessica E., Shapiro, Adam J., Carson, Johnny L., Krischer, Jeffrey, Hazucha, Milan J., Knowles, Michael R.
Formato: Artigo
Idioma:Inglês
Publicado em: American Thoracic Society 2016
Assuntos:
Original Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5021075/
https://ncbi.nlm.nih.gov/pubmed/27070726
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1513/AnnalsATS.201511-748OC
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