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Journal of Human Genetics|December 28, 2007
Association of an intronic haplotype of the LIPC gene with hyperalphalipoproteinemia in two independent populationsHiroshi Iijima, Mitsuru Emi, Manabu Wada, et al.
Human Genetics|January 17, 2004
A mutation in PCSK9 causing autosomal-dominant hypercholesterolemia in a Utah pedigreeKirsten M Timms, Susanne Wagner, Mark E Samuels, et al.
Hypertension (Dallas, Tex. : 1979)|January 1, 1991
Genetic traits related to hypertension and electrolyte metabolismR R Williams, S J Hasstedt, S C Hunt, et al.
Archives of Internal Medicine|March 1, 1990
Population-based frequency of dyslipidemia syndromes in coronary-prone families in UtahR R Williams, P N Hopkins, S C Hunt, et al.
The Journal of Pediatrics|November 3, 2009
Colesevelam hydrochloride: efficacy and safety in pediatric subjects with heterozygous familial hypercholesterolemiaEvan A Stein, A David Marais, Tamas Szamosi, et al.
Proceedings of Spie--The International Society for Optical Engineering|August 21, 2012
Evaluation of intracranial aneurysm coil embolization in phantoms and patients using a high-resolution Microangiographic Fluoroscope (MAF)Ciprian N Ionita, Amit Jain, Brendan Loughran, et al.
Metabolism: Clinical and Experimental|November 15, 2011
Replication and meta-analysis of the gene-environment interaction between body mass index and the interleukin-6 promoter polymorphism with higher insulin resistancePatricia C Underwood, Bindu Chamarthi, Jonathan S Williams, et al.
The Journal of Clinical Endocrinology and Metabolism|March 11, 2021
Characterizing a Common CERS2 Polymorphism in a Mouse Model of Metabolic Disease and in Subjects from the Utah CAD StudyRebekah J Nicholson, Annelise M Poss, J Alan Maschek, et al.
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