Primary Ciliary Dyskinesia: Longitudinal Study of Lung Disease by Ultrastructure Defect and Genotype

Rationale: In primary ciliary dyskinesia, factors leading to disease heterogeneity are poorly understood. Objectives: To describe early lung disease progression in primary ciliary dyskinesia and identify associations between ultrastructural defects and genotypes with clinical phenotype. Methods: Thi...

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Pubblicato in:Am J Respir Crit Care Med
Autori principali: Davis, Stephanie D., Rosenfeld, Margaret, Lee, Hye-Seung, Ferkol, Thomas W., Sagel, Scott D., Dell, Sharon D., Milla, Carlos, Pittman, Jessica E., Shapiro, Adam J., Sullivan, Kelli M., Nykamp, Keith R., Krischer, Jeffrey P., Zariwala, Maimoona A., Knowles, Michael R., Leigh, Margaret W.
Natura: Artigo
Lingua:Inglês
Pubblicazione: American Thoracic Society 2019
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Original Articles
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6353004/
https://ncbi.nlm.nih.gov/pubmed/30067075
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1164/rccm.201803-0548OC
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