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Pulmonary alveolar proteinosis, a primary immunodeficiency of impaired GM-CSF stimulation of macrophages

Pulmonary alveolar proteinosis (PAP) is a rare syndrome characterized by accumulation of pulmonary surfactant, respiratory insufficiency, and increased infections. It occurs in various clinical settings that disrupt surfactant catabolism in alveolar macrophages, including a relatively more common au...

詳細記述

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書誌詳細
主要な著者: Trapnell, Bruce C., Carey, Brenna C., Uchida, Kanji, Suzuki, Takuji
フォーマット: Artigo
言語:Inglês
出版事項: 2009
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC2779868/
https://ncbi.nlm.nih.gov/pubmed/19796925
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.coi.2009.09.004
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