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Vinaya Simha

Showing results (31-40 of 63) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|June 6, 2003
Genetic and phenotypic heterogeneity in patients with mandibuloacral dysplasia-associated lipodystrophyVinaya Simha, Anil K Agarwal, Elif Arioglu Oral, et al.
American Journal of Preventive Cardiology|April 25, 2023
Dramatic elevation of LDL cholesterol from ketogenic-dieting: A Case SeriesTyler Schmidt, David M Harmon, Erica Kludtke, et al.
Diabetes Care|December 28, 2002
Effect of leptin replacement on intrahepatic and intramyocellular lipid content in patients with generalized lipodystrophyVinaya Simha, Lidia S Szczepaniak, Anthony J Wagner, et al.
Hepatology (Baltimore, Md.)|June 6, 2021
Familial Hypobetalipoproteinemia: An Underrecognized Cause of Lean NASHSeth Buryska, Joseph C Ahn, Alina M Allen, et al.
European Journal of Endocrinology|March 1, 2013
Cholic acid for hepatic steatosis in patients with lipodystrophy: a randomized, controlled trialZahid Ahmad, Lalitha Subramanyam, Lidia Szczepaniak, et al.
American Journal of Medical Genetics. Part A|August 14, 2008
Novel subtype of congenital generalized lipodystrophy associated with muscular weakness and cervical spine instabilityVinaya Simha, Anil K Agarwal, Patricia A Aronin, et al.
Metabolic Syndrome and Related Disorders|November 12, 2024
Truncated Albumins as Novel Surrogate Biomarkers in Diabetes Therapy: Epiphenomena and Potential Clinical ApplicationsMadhumati S Vaishnav, Namita Kumari, Sathyanarayana Srikanta, et al.
Journal of Intensive Care Medicine|May 15, 2025
Propofol-associated Hypertriglyceridemia: Development and Multicenter Validation of a Machine-Learning-Based Prediction ToolJiawen Deng, Kiyan Heybati, Keshav Poudel, et al.
The Journal of Clinical Endocrinology and Metabolism|February 26, 2026
Genotype-Phenotype Heterogeneity Among Patients with Lipodystrophy Harboring Rare POLD1 VariantsFieke W Hoff, Chao Xing, Chun-Yuan Huang, et al.
The Journal of Clinical Endocrinology and Metabolism|December 16, 2011
Comparison of efficacy and safety of leptin replacement therapy in moderately and severely hypoleptinemic patients with familial partial lipodystrophy of the Dunnigan varietyVinaya Simha, Lalitha Subramanyam, Lidia Szczepaniak, et al.
Pageof 7

Showing results (31-40 of 63) with videos related to

Sort By:
Pageof 7
The Journal of Clinical Endocrinology and Metabolism|June 6, 2003
Genetic and phenotypic heterogeneity in patients with mandibuloacral dysplasia-associated lipodystrophyVinaya Simha, Anil K Agarwal, Elif Arioglu Oral, et al.
American Journal of Preventive Cardiology|April 25, 2023
Dramatic elevation of LDL cholesterol from ketogenic-dieting: A Case SeriesTyler Schmidt, David M Harmon, Erica Kludtke, et al.
Diabetes Care|December 28, 2002
Effect of leptin replacement on intrahepatic and intramyocellular lipid content in patients with generalized lipodystrophyVinaya Simha, Lidia S Szczepaniak, Anthony J Wagner, et al.
Hepatology (Baltimore, Md.)|June 6, 2021
Familial Hypobetalipoproteinemia: An Underrecognized Cause of Lean NASHSeth Buryska, Joseph C Ahn, Alina M Allen, et al.
European Journal of Endocrinology|March 1, 2013
Cholic acid for hepatic steatosis in patients with lipodystrophy: a randomized, controlled trialZahid Ahmad, Lalitha Subramanyam, Lidia Szczepaniak, et al.
American Journal of Medical Genetics. Part A|August 14, 2008
Novel subtype of congenital generalized lipodystrophy associated with muscular weakness and cervical spine instabilityVinaya Simha, Anil K Agarwal, Patricia A Aronin, et al.
Metabolic Syndrome and Related Disorders|November 12, 2024
Truncated Albumins as Novel Surrogate Biomarkers in Diabetes Therapy: Epiphenomena and Potential Clinical ApplicationsMadhumati S Vaishnav, Namita Kumari, Sathyanarayana Srikanta, et al.
Journal of Intensive Care Medicine|May 15, 2025
Propofol-associated Hypertriglyceridemia: Development and Multicenter Validation of a Machine-Learning-Based Prediction ToolJiawen Deng, Kiyan Heybati, Keshav Poudel, et al.
The Journal of Clinical Endocrinology and Metabolism|February 26, 2026
Genotype-Phenotype Heterogeneity Among Patients with Lipodystrophy Harboring Rare POLD1 VariantsFieke W Hoff, Chao Xing, Chun-Yuan Huang, et al.
The Journal of Clinical Endocrinology and Metabolism|December 16, 2011
Comparison of efficacy and safety of leptin replacement therapy in moderately and severely hypoleptinemic patients with familial partial lipodystrophy of the Dunnigan varietyVinaya Simha, Lalitha Subramanyam, Lidia Szczepaniak, et al.
Pageof 7