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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發表在: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.
格式: Artigo
語言:Inglês
出版: American Thoracic Society 2016
主題:
Original Research
在線閱讀: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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