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The Journal of Clinical Endocrinology and Metabolism
|
June 6, 2003
Genetic and phenotypic heterogeneity in patients with mandibuloacral dysplasia-associated lipodystrophy
Vinaya 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 Series
Tyler 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 lipodystrophy
Vinaya Simha, Lidia S Szczepaniak, Anthony J Wagner, et al.
Hepatology (Baltimore, Md.)
|
June 6, 2021
Familial Hypobetalipoproteinemia: An Underrecognized Cause of Lean NASH
Seth 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 trial
Zahid 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 instability
Vinaya 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 Applications
Madhumati 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 Tool
Jiawen 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 Variants
Fieke 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 variety
Vinaya Simha, Lalitha Subramanyam, Lidia Szczepaniak, et al.
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of 7
Search research articles
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Showing results (31-40 of 63) with videos related to
Sort By:
Page
of 7
The Journal of Clinical Endocrinology and Metabolism
|
June 6, 2003
Genetic and phenotypic heterogeneity in patients with mandibuloacral dysplasia-associated lipodystrophy
Vinaya 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 Series
Tyler 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 lipodystrophy
Vinaya Simha, Lidia S Szczepaniak, Anthony J Wagner, et al.
Hepatology (Baltimore, Md.)
|
June 6, 2021
Familial Hypobetalipoproteinemia: An Underrecognized Cause of Lean NASH
Seth 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 trial
Zahid 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 instability
Vinaya 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 Applications
Madhumati 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 Tool
Jiawen 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 Variants
Fieke 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 variety
Vinaya Simha, Lalitha Subramanyam, Lidia Szczepaniak, et al.
Page
of 7