Results 61 to 70 of about 423,899 (348)

Echocardiographic assessment of pulmonary hypertension: a guideline protocol from the British Society of Echocardiography. [PDF]

, 2018
Pulmonary hypertension is defined as a mean arterial pressure of ≥25 mmHg as confirmed on right heart catheterisation. Traditionally, the pulmonary arterial systolic pressure has been estimated on echo by utilising the simplified Bernoulli equation from ...
Augustine, DX, Bhattacharyya, S, British Society of Echocardiography Education Committee,, Coates-Bradshaw, LD, Coghlan, G, Fox, K, Grapsa, J, Harkness, A, Howard, LS, Kaye, N, Mathew, T, Nihoyannopoulos, P, Oxborough, D, Rana, BS, Ring, L, Robinson, S, Sandoval, J, Sharma, V, Siva, A, Steeds, RP, Willis, J   +20 more
core   +3 more sources

Endothelial-to-Mesenchymal Transition in Pulmonary Arterial Hypertension.

Antioxidants and Redox Signaling, 2020
Endothelial-to-Mesenchymal transition (EndMT) is a process which encompasses extensive transcriptional reprogramming of activated endothelial cells leading to a shift towards mesenchymal cellular phenotypes and functional responses. Initially observed in
A. Gorelova, M. Berman, I. Al Ghouleh
semanticscholar   +1 more source

Endothelin receptor antagonists in a beagle model of pulmonary hypertension: Contribution to possible potential therapy? [PDF]

, 1995
Objectives.This study investigated the pharmacologic effect of endothelin receptor antagonists on cardiopulmonary hemodynamic variables in a beagle model of pulmonary hypertension.Background.We recently developed a beagle model of pulmonary hypertension ...
Okada, Kenji, Okada, Masayoshi, Okada, Morihito, Yamashita, Chojiro   +3 more
core   +1 more source

Plasma proteome analysis in patients with pulmonary arterial hypertension: an observational cohort study [PDF]

, 2017
BackgroundIdiopathic and heritable pulmonary arterial hypertension form a rare but molecularly heterogeneous disease group. We aimed to measure and validate differences in plasma concentrations of proteins that are associated with survival in patients ...
Abdul-Salam, Ahmad, Benza, Benza, D'Alonzo, Delafontaine, Galie, Ganz, Geraci, Gold, Hansmann, Humbert, Johnson, Kundu, Kwapiszewska, Lavoie, Lepetit, Machado, McGoon, Nickel, Pencina, Rhodes, Rhodes, Schermuly, Shah, Soon, Vander, Walport, Weinberg, Weinberg   +29 more
core   +1 more source

Caracterización clínica, funcional y hemodinámica de la población con hipertensión pulmonar arterial evaluada en el Instituto Nacional del Tórax [PDF]

, 2006
Pulmonary Arterial Hypertension is a rare, progressive and devastating disease with severe consequences in quality of life and survival. Aim: A clinical, functional and hemodynamic assessment of patients with pulmonary arterial hypertension and ...
Parra R., Claudio, Uriarte G. de C., Polentzi, Wainstein G., Eduardo, Zagolin B., Mónica   +3 more
core   +1 more source

ACVIM consensus statement guidelines for the diagnosis, classification, treatment, and monitoring of pulmonary hypertension in dogs. [PDF]

, 2020
Pulmonary hypertension (PH), defined by increased pressure within the pulmonary vasculature, is a hemodynamic and pathophysiologic state present in a wide variety of cardiovascular, respiratory, and systemic diseases.
Abbott, Jonathan, Borgarelli, Michele, Clercx, Cécile, Kellihan, Heidi B, Masseau, Isabelle, Reinero, Carol, Rozanski, Elizabeth, Scansen, Brian A, Visser, Lance C, Williams, Kurt   +9 more
core   +3 more sources

Pulmonary arterial hypertension: the burden of disease and impact on quality of life. [PDF]

, 2015
Pulmonary arterial hypertension (PAH) is a debilitating disease that pervades all aspects of a patients daily life. It is also increasingly acknowledged that the burden of PAH extends to older patients and carers.
Delcroix, M, Howard, L
core   +6 more sources

Actualización en el diagnóstico y terapéutica en hipertensión pulmonar arterial [PDF]

, 2006
Indexación: ScieloResumen: Pulmonary Arterial Hypertension includes a heterogeneous group of disorders with a common genetic, pathological and hemodinamyc origin.
Uriarte G., Polentzi, Wainstein G., Eduardo, Zagolin B., Mónica   +2 more
core   +1 more source

Pregnancy in pulmonary arterial hypertension [PDF]

European Respiratory Review, 2016
Despite advanced therapies, maternal mortality in women with pulmonary arterial hypertension (PAH) remains high in pregnancy and is especially high during the post-partum period. However, recent data indicates that morbidity and mortality during pregnancy and after birth have improved for PAH patients.
Karen M. Olsson, Richard N. Channick
openaire   +4 more sources

Obesity, estrogens and adipose tissue dysfunction – implications for pulmonary arterial hypertension

Pulmonary Circulation, 2020
Obesity is a prevalent global public health issue characterized by excess body fat. Adipose tissue is now recognized as an important endocrine organ releasing an abundance of bioactive adipokines including, but not limited to, leptin, adiponectin and ...
K. Mair, R. Gaw, M. MacLean
semanticscholar   +1 more source