Characteristics of a Large Cohort of Patients with Autoimmune Pulmonary Alveolar Proteinosis in Japan

Rationale: Acquired pulmonary alveolar proteinosis (PAP) is a syndrome characterized by pulmonary surfactant accumulation occurring in association with granulocyte/macrophage colony-stimulating factor autoantibodies (autoimmune PAP) or as a consequence of another disease (secondary PAP). Because PAP...

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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Inoue, Yoshikazu, Trapnell, Bruce C., Tazawa, Ryushi, Arai, Toru, Takada, Toshinori, Hizawa, Nobuyuki, Kasahara, Yasunori, Tatsumi, Koichiro, Hojo, Masaaki, Ichiwata, Toshio, Tanaka, Naohiko, Yamaguchi, Etsuro, Eda, Ryosuke, Oishi, Kazunori, Tsuchihashi, Yoshiko, Kaneko, Chinatsu, Nukiwa, Toshihiro, Sakatani, Mitsunori, Krischer, Jeffrey P., Nakata, Koh
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: American Thoracic Society 2008
Gaiak:
D. Interstitial Lung Disease
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC2720118/
https://ncbi.nlm.nih.gov/pubmed/18202348
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1164/rccm.200708-1271OC
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