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Potential benefit of bosentan therapy in borderline or less severe pulmonary hypertension secondary to idiopathic pulmonary fibrosis—an interim analysis of results from a prospective, single-center, randomized, parallel-group study

BACKGROUND: No drugs have been approved for the treatment of patients with pulmonary hypertension (PH) secondary to idiopathic pulmonary fibrosis (IPF), particularly those with idiopathic honeycomb lung. This study was conducted to investigate the long-term efficacy and safety of bosentan for PH bas...

詳細記述

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書誌詳細
出版年:BMC Pulm Med
主要な著者: Tanaka, Yosuke, Hino, Mitsunori, Gemma, Akihiko
フォーマット: Artigo
言語:Inglês
出版事項: BioMed Central 2017
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC5729252/
https://ncbi.nlm.nih.gov/pubmed/29237441
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12890-017-0523-2
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