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See Latest ArticlesNovel LMF1 Nonsense Mutation in a Patient with Severe Hypertriglyceridemia
Journal of Clinical Endocrinology and Metabolism, 10/15/09
Cefalu AB et al. – The authors identified the second novel pathogenic mutation in LMF1 gene in a patient with severe hypertriglyceridemia. LPL deficiency in the patient was milder than in the carrier of the Y439X previously described.
Today in Atherosclerosis/Lipids...keeping you current
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Nutritional supplements and serum lipids: Does anything work
Current Atherosclerosis Reports, 11/16/09
Carbohydrate-restricted diets for obesity and related diseases: An update
Current Atherosclerosis Reports, 11/17/09
Systematic Review: Comparative Effectiveness and Harms of Combination Therapy and Monotherapy for Dyslipidemia
Annals of Internal Medicine, 11/03/09
Today in Basic Science/Genetics...keeping you current
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Cytotoxic T lymphocyte antigen-4 Ala17 polymorphism is a genetic marker of autoimmune adrenal insufficiency: Italian association study and meta-analysis of European studies
European Journal of Endocrinology, 11/05/09
PTH and IL21R May Underlie Variation of Femoral Neck Bone Mineral Density as Revealed by a Genome-Wide Association Study
Journal of Bone and Mineral Research, 11/03/09
Hip Geometry Variation is Associated With Bone Mineralization Pathway Gene Variants: The Framingham Study
Journal of Bone and Mineral Research, 11/13/09
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