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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...

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Publicat a:BMC Pulm Med
Autors principals: Tanaka, Yosuke, Hino, Mitsunori, Gemma, Akihiko
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2017
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Accés en línia: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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