Results 161 to 170 of about 423,899 (348)
Annals of Thoracic Medicine, 2014 Aims: The main objective of this study is to describe patients′ clinical characteristics and physiological and hemodynamic parameters at the time of diagnosis in a pulmonary hypertension center in Saudi Arabia.
M M Idrees +10 more
doaj +1 more source
Fulminating arterial hypertension with pulmonary edema from release of adrenomedullary catecholamines after lesions of the anterior hypothalamus in the rat. [PDF]
, 1975 Marc A. Nathan, D.J. Reis
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Animal Models and Experimental Medicine, EarlyView.This study investigated changes in pulmonary artery hemodynamics using a Flowire catheter and evaluated the accuracy of Doppler echocardiography in dogs with acute pulmonary thromboembolism (PTE). Ten healthy beagles were anesthetized, and acute pulmonary hypertension (PH) was induced by injecting 300‐μm dextran microspheres.
Tomohiko Yoshida +3 more
wiley +1 more source
Vascular Changes During Resolution Of Pulmonary Arterial Hypertension [PDF]
, 1981 Clarence A. Rawlings +2 more
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The role of endothelin-1 in pulmonary arterial hypertension. [PDF]
, 2014 Pulmonary arterial hypertension (PAH) is a rare but debilitating disease, which if left untreated rapidly progresses to right ventricular failure and eventually death. In the quest to understand the pathogenesis of this disease differences in the profile,
Chester, AH, Yacoub, MH
core +1 more source
The Anatomical Record, EarlyView.Abstract Autonomic nerves are crucial in cardiac function and pathology. However, data on the distribution of cholinergic and noradrenergic nerves in normal and pathologic human hearts is lacking. Nonfailing donor hearts were pressure‐perfusion fixed, imaged, and dissected. Left ventricular cardiomyopathy samples were also obtained.
Peter Hanna +15 more
wiley +1 more source
The Myogenic Response of Arterial Vessels Is Increased in Fetal Pulmonary Hypertension [PDF]
, 1995 Jaques Belik
openalex +1 more source
Pulmonary Arterial Hypertension: Pathophysiology and Treatment
Diseases, 2018 Pulmonary arterial hypertension (PAH), the first category of pulmonary hypertension, is a chronic and progressive disorder characterised by angioproliferative vasculopathy in the pulmonary arterioles, leading to endothelial and smooth muscle ...
Norris S H Lan +3 more
semanticscholar +1 more source
Understanding pulmonary arterial hypertension
Nursing Management (Springhouse), 2004 New therapies improve the management of pulmonary arterial hypertension.
openaire +6 more sources
Arthritis &Rheumatology, EarlyView.Objective An unmet need exists for glucocorticoid‐sparing treatments for patients with polymyalgia rheumatica (PMR). The antibody‐drug conjugate ABBV‐154 comprises adalimumab conjugated to a glucocorticoid receptor modulator. We evaluated ABBV‐154 versus placebo in patients with glucocorticoid‐dependent PMR.
Robert F. Spiera +14 more
wiley +1 more source