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Atherosclerosis|February 18, 2011
Association of gene variants with lipid levels in response to fenofibrate is influenced by metabolic syndrome statusMary F Feitosa, Ping An, Jose M Ordovas, et al.
Japanese Heart Journal|December 28, 1999
Familial hypercholesterolemia in Utah kindred with novel R103W mutations in exon 4 of the LDL receptor geneH Katsumata, M Emi, Y Nobe, et al.
The Journal of Clinical Endocrinology and Metabolism|July 9, 2004
Thyroid function and blood pressure homeostasis in euthyroid subjectsOlga Gumieniak, Todd S Perlstein, Paul N Hopkins, et al.
Experimental Gerontology|September 16, 2008
Serum bilirubin levels, UGT1A1 polymorphisms and risk for coronary artery diseaseArno Lingenhel, Barbara Kollerits, Johannes P Schwaiger, et al.
AJNR. American Journal of Neuroradiology|July 16, 2011
Evaluation of a second-generation self-expanding variable-porosity flow diverter in a rabbit elastase aneurysm modelC N Ionita, S K Natarajan, W Wang, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|October 16, 2023
Obesity does not alter vascular function and handgrip exercise hemodynamics in middle-aged patients with hypertensionStephen M Ratchford, Ryan M Broxterman, D Taylor La Salle, et al.
Atherosclerosis|May 12, 2004
TXNIP gene not associated with familial combined hyperlipidemia in the NHLBI Family Heart StudyHilary Coon, Nanda Singh, Diane Dunn, et al.
Klinische Wochenschrift|January 1, 1990
Concordant dyslipidemia, hypertension and early coronary disease in Utah familiesR R Williams, S C Hunt, L L Wu, et al.
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