Results 111 to 120 of about 274,289 (156)

PULMONARY HYPERTENSION

Nihon Naika Gakkai Zasshi, 1978
openaire   +3 more sources

Pulmonary Hypertension and Mortality in Patients Awaiting Kidney Transplant: Cause for Concern and Potential Opportunity. [PDF]

, 2020
Bokoch, Michael P, Findlay, James Y
core   +1 more source

IDIOPATHIC PULMONARY HYPERTENSION [PDF]

Heart, 1957
J W, BROWN, D, HEATH, W, WHITAKER
openaire   +2 more sources

Survival in patients with pulmonary hypertension associated with fibrotic interstitial lung disease (ILD) is independent of ILD subtype

ERJ Open Research
Ifan Jenkin, Konstantinos Dimopoulos, Steven D. Nathan, Sophie Herbert, Timothy Dawes, Simon Bax, Colm McCabe, Heba Nashat, Bhavin Rawal, Bhashkar Mukherjee, Vasilis Kouranos, Maria Kokosi, Athol U. Wells, Elisabetta Renzoni, Philip Molyneaux, Gisli Jenkins, Peter M. George, S. John Wort, Laura Claire Price   +18 more
doaj   +1 more source

Pulmonary arterial hypertension exacerbated by ruxolitinib

Haematologica, 2015
Andrew T. Low, Luke Howard, Claire Harrison, Robert M.R. Tulloh   +3 more
doaj   +1 more source

Corrigendum to “Exercise ventilatory reserve predicts survival in adult congenital heart disease associated pulmonary arterial hypertension with Eisenmenger physiology” [Int J Cardiol Congenit Heart Dis, Volume 7, March 2022, 100331]

International Journal of Cardiology Congenital Heart Disease
Chinthaka B. Samaranayake, Ruth McNiven, Aleksander Kempny, Carl Harries, Laura C. Price, Michael Gatzoulis, Konstantinos Dimopoulos, Stephen J. Wort, Colm McCabe   +8 more
doaj   +1 more source

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Pulmonary hypertension

Drugs of Today, 1998
Pulmonary hypertension can be caused by an increase in pulmonary blood flow, an increase in left-heart impedance or an increase in pulmonary vascular resistance. Although there are many specific causes that have been identified, clinical presentation and natural history are common to all etiologies.
D, Moraes, J, Loscalzo
openaire   +2 more sources

Pulmonary hypertension

Nursing Standard, 2002
Pulmonary hypertension (PH) is a rare blood vessel disorder of the lung, in which the pressure in the pulmonary artery rises above normal levels and can become life-threatening. The authors discuss the disease process, symptoms, investigations and patient management.
Paula, Rogers, Iain, Armstrong
openaire   +2 more sources

Pulmonary Hypertension

Medical Clinics of North America, 2019
Pulmonary hypertension (PH) is a chronic and progressive disease that presents like many other lung diseases, often leading to a delay in diagnosis, and therefore a delay in optimal therapy. This article provides a review of PH for internists, covering clinical presentation, diagnostic algorithm, different types of PH, and overview of treatments.
Darlene, Kim, M Patricia, George
openaire   +2 more sources

Pulmonary arterial hypertension

Current Atherosclerosis Reports, 2009
Pulmonary arterial hypertension is a progressive disease of pulmonary vasculature characterized by increased mean pulmonary arterial pressure and elevated vascular resistance with normal left-sided pressures, differentiating it from left-sided heart disease.
Aydin, Uzunpinar, Mehmet, Cilingiroglu
openaire   +2 more sources