Hereditary Pulmonary Alveolar Proteinosis: Pathogenesis, Presentation, Diagnosis, and Therapy

Rationale: We identified a 6-year-old girl with pulmonary alveolar proteinosis (PAP), impaired granulocyte-macrophage colony–stimulating factor (GM-CSF) receptor function, and increased GM-CSF. Objectives: Increased serum GM-CSF may be useful to identify individuals with PAP caused by GM-CSF recepto...

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Detalhes bibliográficos
Main Authors: Suzuki, Takuji, Sakagami, Takuro, Young, Lisa R., Carey, Brenna C., Wood, Robert E., Luisetti, Maurizio, Wert, Susan E., Rubin, Bruce K., Kevill, Katharine, Chalk, Claudia, Whitsett, Jeffrey A., Stevens, Carrie, Nogee, Lawrence M., Campo, Ilaria, Trapnell, Bruce C.
Formato: Artigo
Idioma:Inglês
Publicado em: American Thoracic Society 2010
Assuntos:
F. Pediatrics and Lung Development
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3001266/
https://ncbi.nlm.nih.gov/pubmed/20622029
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1164/rccm.201002-0271OC
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