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Pulmonary Circulation|February 12, 2024
Using PAH-SYMPACT to assess quality of life in patients with pulmonary hypertension associated with chronic lung diseaseMorgan E Bailey, Louise Durst, Hector R Cajigas, et al.
Transplantation|November 27, 2008
Sirolimus as primary immunosuppressant reduces left ventricular mass and improves diastolic function of the cardiac allograftEugenia Raichlin, Krishnaswamy Chandrasekaran, Walter K Kremers, et al.
European Journal of Human Genetics : EJHG|February 1, 2007
Recurrent rearrangements in the proximal 15q11-q14 region: a new breakpoint cluster specific to unbalanced translocationsCécile Mignon-Ravix, Danielle Depetris, Judith J Luciani, et al.
Journal of the American Heart Association|April 27, 2022
Mortality in Pulmonary Arterial Hypertension in the Modern Era: Early Insights From the Pulmonary Hypertension Association RegistryKevin Y Chang, Sue Duval, David B Badesch, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|August 14, 2012
World Health Organization Pulmonary Hypertension group 2: pulmonary hypertension due to left heart disease in the adult--a summary statement from the Pulmonary Hypertension Council of the International Society for Heart and Lung TransplantationJames C Fang, Teresa DeMarco, Michael M Givertz, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|January 18, 2003
Clinical predictors of exercise capacity 1 year after cardiac transplantationTat-Chi Leung, Karla V Ballman, Thomas G Allison, et al.
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