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Pulmonary Arterial Hypertension
New England Journal of Medicine, 2021 Abstract: This article discusses the pathophysiology, risk factors, clinical manifestations, diagnostics, and pharmacologic treatment of pulmonary arterial hypertension, as well as nursing considerations for caring for patients with this rare disease.
Paul M Hassoun
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Pulmonary arterial hypertension
Medicina Clínica (English Edition), 2022Pulmonary 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
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Pulmonary Arterial Hypertension
New England Journal of Medicine, 2004Joseph Loscalzo, Harrison W Farber
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Pulmonary arterial hypertension
La Presse Médicale, 2023Pulmonary 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
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Pulmonary Arterial Hypertension
Current Problems in Cardiology, 2011Pulmonary 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
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Pulmonary Arterial Hypertension
Heart Failure Clinics, 2018This 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
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Pulmonary Arterial Hypertension
Current Vascular Pharmacology, 2010The 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
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Management of Pulmonary Arterial Hypertension
Seminars in Respiratory and Critical Care Medicine, 2023AbstractPulmonary arterial hypertension (PAH) is a rare pulmonary vascular disease characterized by progressive pulmonary arterial remodeling, increased pulmonary vascular resistance, right ventricular dysfunction, and reduced survival. Effective therapies have been developed that target three pathobiologic pathways in PAH: nitric oxide, endothelin-1 ...
Jason, Weatherald +3 more
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Pulmonary arterial hypertension in women
Revue des Maladies Respiratoires, 2010Pulmonary arterial hypertension (PAH) is a rare condition characterized by sustained elevation in pulmonary arterial resistance leading to right heart failure.PAH afflicts predominantly women. Echocardiography is the initial investigation of choice for non-invasive detection of PAH but right-heart catheterization is necessary to confirm the diagnosis ...
O, Sanchez +5 more
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Echocardiography in Pulmonary Arterial Hypertension
Current Cardiology Reports, 2019Pulmonary arterial hypertension (PAH) is a devastating disease which can result in right heart (RH) failure and death. Herein, we discuss the current clinical applications of echocardiography in PAH.Advanced echocardiographic techniques (strain, strain rate, 2D-speckle tracking strain, and three-dimensional echocardiography) may reveal in the near ...
Ferrara F. +9 more
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