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Pulmonary Hypertension in Idiopathic Pulmonary Fibrosis
Chest, 2007Idiopathic pulmonary fibrosis (IPF) is an untreatable diffuse parenchymal lung disease with a median survival of < 3 years. Pulmonary hypertension (PH) is frequently seen in patients with IPF and is commonly attributed to hypoxic vasoconstriction and capillary destruction. Pathology findings include endothelial proliferation and medial hypertrophy that
David J. Lederer+3 more
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2019
Chronic interstitial lung disease (ILD) is considered a heterogeneous group of pulmonary diseases usually classified on the basis of clinical, radiological and histological aspects, characterized by a variable degree of inflammation and fibrosis. The most diagnosed ILD are idiopathic pulmonary fibrosis (IPF), characterized by the presence of serious ...
Assunta Micco, M. Del Donno, A. Di Sorbo
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Chronic interstitial lung disease (ILD) is considered a heterogeneous group of pulmonary diseases usually classified on the basis of clinical, radiological and histological aspects, characterized by a variable degree of inflammation and fibrosis. The most diagnosed ILD are idiopathic pulmonary fibrosis (IPF), characterized by the presence of serious ...
Assunta Micco, M. Del Donno, A. Di Sorbo
openaire +2 more sources
A Phase 3 Trial of Pirfenidone in Patients with Idiopathic Pulmonary Fibrosis
Yearbook of Pulmonary Disease, 2015Tomohiro Handa, Arata Azuma
semanticscholar +1 more source
Diagnostic criteria for idiopathic pulmonary fibrosis: a Fleischner Society White Paper.
The Lancet Respiratory Medicine, 2017D. Lynch+16 more
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Sildenafil in Idiopathic Pulmonary Fibrosis
New England Journal of Medicine, 2010ROSSI, GIANPAOLO, SECCIA, TERESA MARIA
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Pirfenidone in patients with idiopathic pulmonary fibrosis (CAPACITY): two randomised trials
The Lancet, 2011P. Noble+11 more
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Seminars in Respiratory and Critical Care Medicine, 1984
Nell Pape Waring+2 more
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Nell Pape Waring+2 more
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