Results 211 to 220 of about 173,364 (256)

Quality of life in patients with pulmonary arterial hypertension: A systematic review and meta-analysis. [PDF]

Health Qual Life Outcomes
Carmona-Segovia AD, Morales-Asencio JM, Escribano-Subías P, Rodríguez-Capitán J, Jiménez-Navarro M, Becerra-Muñoz VM.   +5 more
europepmc   +1 more source

Amonafide Targeting NTSR1-PI3K/AKT/mTOR Signaling Attenuates Vascular Remodeling in Pulmonary Arterial Hypertension. [PDF]

J Am Heart Assoc
Zhu YJ, Kou JJ, Bo YC, Zhang MJ, Fan X, Zhao LL, Yan Y, Zhang HD, Wu WH, Yuan P, Liu Y, Shi JZ, Pang XB, He YY.   +13 more
europepmc   +1 more source

Targeting the Hippo pathway in pulmonary arterial hypertension: emerging pharmacological strategies. [PDF]

J Hypertens
Zheng D, Guo Y.
europepmc   +1 more source

Reduced Circulating HIF-1α, HIF-2α, HIF-3α, and VHL Levels in Patients With Pulmonary Arterial Hypertension. [PDF]

Pulm Circ
Kan H, Alsancak Y, Uyaner Kan M, Göktaş E, Çelik M, Gürbüz AS, Düzenli MA.   +6 more
europepmc   +1 more source

Transitioning From Oral to Intravenous Treprostinil in Pulmonary Arterial Hypertension: A Case Report. [PDF]

Clin Case Rep
Cummings AM, Konkol SB, Mihalek AD, Roth ME.   +3 more
europepmc   +1 more source

Methamphetamine-Associated Pulmonary Arterial Hypertension: Impact, Mechanisms, and a Framework for Management. [PDF]

Pulm Circ
Sood N, Weerasekare J, Zhyvylo I, Goncharova EA, De Marco T.   +4 more
europepmc   +1 more source

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
exaly   +8 more sources

Some of the next articles are maybe not open access.

Related searches:

Pulmonary Arterial Hypertension

New England Journal of Medicine, 2004
Harrison Farber, Joseph Loscalzo, Loscalzo Joseph   +2 more
exaly   +3 more sources

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, Alicia, Ruiz Martín, Pilar, Escribano Subías   +2 more
openaire   +2 more sources