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Idiopathic Pulmonary Fibrosis

New England Journal of Medicine, 2018
Idiopathic Pulmonary Fibrosis Idiopathic pulmonary fibrosis appears to be increasing in incidence. It requires early recognition and intervention with supportive care and pharmacologic agents to forestall its progression. Lung transplantation may be curative, but the disease may recur in transplanted lungs.
David J Lederer, Fernando J Martinez
exaly   +8 more sources

Idiopathic Pulmonary Fibrosis

New England Journal of Medicine, 2001
Idiopathic pulmonary fibrosis is a rapidly progressive illness of unknown cause characterized by sequential acute lung injury with subsequent scarring and end-stage lung disease. Treatment at present remains largely supportive, with evidence that patients' satisfaction and survival may be improved by referral to centers specializing in the evaluation ...
G W Hunninghake, T J Gross
exaly   +3 more sources

Idiopathic Pulmonary Fibrosis and Progressive Pulmonary Fibrosis

Immunology and Allergy Clinics of North America, 2023
Idiopathic pulmonary fibrosis (IPF), a common interstitial lung disease (ILD), is a chronic, progressive fibrosing interstitial pneumonia, with an unknown cause. IPF has been linked to several genetic and environmental risk factors. Disease progression is common and associated with worse outcomes.
Rachel, Strykowski, Ayodeji, Adegunsoye
openaire   +2 more sources

Idiopathic pulmonary fibrosis

Medicina Clínica (English Edition), 2017
Idiopathic pulmonary fibrosis is a fibrosing interstitial pneumonia associated with the radiological and/or histological pattern of usual interstitial pneumonia. Its aetiology is unknown, but probably comprises the action of endogenous and exogenous micro-environmental factors in subjects with genetic predisposition.
Antoni, Xaubet   +2 more
openaire   +4 more sources

Pulmonary fibrosis

Histopathology, 1990
Diffuse interstitial pulmonary fibrosis is the end result of alveolar damage which may occur as a sudden acute incident or as a slowly developing process. Potentiating factors include release of enzymes and generation of oxygen radicals by granulocytes.
openaire   +2 more sources

Pulmonary fibrosis in children

The Indian Journal of Pediatrics, 1981
The functional integrity of the lung is largely dependant on the connective tissue and capillary structure of the gas exchanging parts. Pulmonary fibrosis as a result of several interstinal diseases have major physiological implications. We report three cases of pulmonary fibrosis in children.
A, Chetty, V P, Choudhry
openaire   +2 more sources

Endothelin in Pulmonary Fibrosis

American Journal of Respiratory Cell and Molecular Biology, 2011
Abstract The endothelin receptor–ligand system includes a family of polypeptides and G-protein–coupled receptors, which, in addition to their classic activity in the regulation of vascular tone (both directly and through the control of nitric oxide), were implicated in a wide variety of other key biological processes.
Carmen, Fonseca   +2 more
openaire   +2 more sources

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