Results 341 to 350 of about 195,645 (350)
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Pulmonary Hypertension in Idiopathic Pulmonary Fibrosis

Chest, 2007
Idiopathic 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
openaire   +3 more sources

Idiopathic pulmonary fibrosis

Meditsinskaya sestra, 2021
Vsevolod V. Skvortsov   +4 more
openaire   +1 more source

Idiopathic Pulmonary Fibrosis

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
openaire   +2 more sources

A Phase 3 Trial of Pirfenidone in Patients with Idiopathic Pulmonary Fibrosis

Yearbook of Pulmonary Disease, 2015
Tomohiro Handa, Arata Azuma
semanticscholar   +1 more source

Diagnostic criteria for idiopathic pulmonary fibrosis: a Fleischner Society White Paper.

The Lancet Respiratory Medicine, 2017
D. Lynch   +16 more
semanticscholar   +1 more source

Pirfenidone in patients with idiopathic pulmonary fibrosis (CAPACITY): two randomised trials

The Lancet, 2011
P. Noble   +11 more
semanticscholar   +1 more source

Idiopathic Pulmonary Fibrosis

Seminars in Respiratory and Critical Care Medicine, 1984
Nell Pape Waring   +2 more
openaire   +2 more sources

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