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Respiratory Investigation|April 15, 2019
Criteria for the diagnosis of idiopathic pleuroparenchymal fibroelastosis: A proposalKentaro Watanabe, Hiroshi Ishii, Fumiaki Kiyomi, et al.
JCI Insight|January 22, 2020
MAPK mutations and cigarette smoke promote the pathogenesis of pulmonary Langerhans cell histiocytosisHuan Liu, Andrew R Osterburg, Jennifer Flury, et al.
Respirology (Carlton, Vic.)|August 9, 2017
Disease severity staging system for idiopathic pulmonary fibrosis in JapanYasuhiro Kondoh, Hiroyuki Taniguchi, Kensuke Kataoka, et al.
Respirology (Carlton, Vic.)|January 21, 2006
Epidemiological and clinical features of idiopathic pulmonary alveolar proteinosis in JapanYoshikazu Inoue, Koh Nakata, Toru Arai, et al.
BMC Pulmonary Medicine|November 5, 2014
Development of microscopic polyangiitis-related pulmonary fibrosis in a patient with autoimmune pulmonary alveolar proteinosisYuhei Kinehara, Hiroshi Kida, Yoshikazu Inoue, et al.
The European Respiratory Journal|December 16, 2014
Safety and pharmacokinetics of nintedanib and pirfenidone in idiopathic pulmonary fibrosisTakashi Ogura, Hiroyuki Taniguchi, Arata Azuma, et al.
BMC Pulmonary Medicine|August 13, 2015
Outcome of corticosteroid administration in autoimmune pulmonary alveolar proteinosis: a retrospective cohort studyKeiichi Akasaka, Takahiro Tanaka, Nobutaka Kitamura, et al.
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