Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
Arteriosclerosis, Thrombosis, and Vascular Biology|October 23, 2012
No shorter telomeres in subjects with a family history of cardiovascular disease in the Asklepios studyTim De Meyer, Caroline M Van Daele, Marc L De Buyzere, et al.
Aging Cell|July 31, 2008
Lower red blood cell counts in middle-aged subjects with shorter peripheral blood leukocyte telomere lengthTim De Meyer, Marc L De Buyzere, Michel Langlois, et al.
European Journal of Cardiovascular Prevention and Rehabilitation : Official Journal of the European Society of Cardiology, Working Groups on Epidemiology & Prevention and Cardiac Rehabilitation and Exercise Physiology|April 21, 2007
Rationale, design, methods and baseline characteristics of the Asklepios StudyErnst-R Rietzschel, Marc L De Buyzere, Sofie Bekaert, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|September 3, 2013
Family history of cardiovascular disease and offspring echocardiographic left ventricular structure and function: the Asklepios StudyCaroline M Van daele, Tim De Meyer, Marc L De Buyzere, et al.
European Heart Journal|August 19, 2009
Systemic telomere length and preclinical atherosclerosis: the Asklepios StudyTim De Meyer, Ernst R Rietzschel, Marc L De Buyzere, et al.
EMBO Reports|November 4, 2021
Involving society in science: Reflections on meaningful and impactful stakeholder engagement in fundamental researchHelen Garrison, Marta Agostinho, Laura Alvarez, et al.
Plos One|October 8, 2011
Practical tools to implement massive parallel pyrosequencing of PCR products in next generation molecular diagnosticsKim De Leeneer, Joachim De Schrijver, Lieven Clement, et al.
Aging Cell|September 19, 2007
Telomere length and cardiovascular risk factors in a middle-aged population free of overt cardiovascular diseaseSofie Bekaert, Tim De Meyer, Ernst R Rietzschel, et al.
BMC Medical Genomics|May 22, 2012
Molecular diagnostics for congenital hearing loss including 15 deafness genes using a next generation sequencing platformSarah De Keulenaer, Jan Hellemans, Steve Lefever, et al.
Pageof 5