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Pulmonary arterial hypertension

Medicina Clínica (English Edition), 2022
Pulmonary arterial hypertension (PAH) is a rare disease characterized by adverse remodeling of the arterial tree leading to increased vascular resistance with subsequent increase in right ventricular afterload and eventual development of heart failure.
Raquel, Luna-López   +2 more
openaire   +2 more sources

Pulmonary Arterial Hypertension

Current Problems in Cardiology, 2011
Pulmonary hypertension is a complex and multidisciplinary disorder. The classification of pulmonary hypertension includes 5 groups. Pulmonary arterial hypertension is a rare disorder that can be idiopathic or heritable in nature, or associated with other conditions, such as scleroderma or congenital heart disease.
Vallerie V, McLaughlin   +2 more
openaire   +4 more sources

Pulmonary arterial hypertension

La Presse Médicale, 2023
Pulmonary arterial hypertension (PAH) is a rare and progressive disease characterised by remodelling of the pulmonary arteries and progressive narrowing of the pulmonary vasculature. This leads to a progressive increase in pulmonary vascular resistance and pulmonary arterial pressure and, if left untreated, to right ventricular failure and death.
Athénaïs Boucly   +7 more
openaire   +2 more sources

Pulmonary Arterial Hypertension

Heart Failure Clinics, 2018
This article provides an overview of pulmonary arterial hypertension (PAH), beginning with the initial pathologic recognition of pulmonary hypertension more than 100 years ago and progressing to the current diagnostic categorization of PAH. It reviews the epidemiology, pathophysiology, genetics, and modern treatment of PAH.
Mark W, Dodson   +2 more
openaire   +2 more sources

Pulmonary Arterial Hypertension

Current Vascular Pharmacology, 2010
The last 10 years have seen significant advances in the understanding of the pathophysiology and treatment of pulmonary arterial hypertension (PAH). This has included new insights into the genetics, cell-signalling pathways and pathological changes seen in the small pulmonary arteries as well as the introduction of new treatments which have improved ...
Christiana, Burt   +2 more
openaire   +2 more sources

Pulmonary Arterial Hypertension in Portal Hypertension

Clinics in Gastroenterology, 1985
Frequence d'estimation difficile; hypertension pulmonaire due a la cirrhose de differentes origines ou consequence d'anastomose porto-cave. Anatomopathologie des vaisseaux pulmonaires. Nature de l'hypertension portale. Etude clinique.
openaire   +2 more sources

The evolving landscape of pulmonary arterial hypertension clinical trials

Lancet, The, 2022
Athénaïs Boucly   +2 more
exaly  

Arterial hypertension

Transplantation Proceedings, 2002
openaire   +2 more sources

Phase 3 Trial of Sotatercept for Treatment of Pulmonary Arterial Hypertension

New England Journal of Medicine, 2023
Marius M Hoeper   +2 more
exaly  

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