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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Detalhes bibliográficos
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: American Thoracic Society 2008
Assuntos:
D. Interstitial Lung Disease
Acesso em linha: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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