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The Journal of Clinical Endocrinology and Metabolism
|
October 6, 2021
Impaired Muscle Mitochondrial Function in Familial Partial Lipodystrophy
Vinaya Simha, Ian R Lanza, Surendra Dasari, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 13, 2024
High LDL Particle and APOB Concentrations in Patients With Adrenal Cortical Adenomas
Rashi Sandooja, Jasmine Saini, Annop Kittithaworn, et al.
The New England Journal of Medicine
|
February 22, 2002
Leptin-replacement therapy for lipodystrophy
Elif Arioglu Oral, Vinaya Simha, Elaine Ruiz, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 30, 2025
Cardiometabolic Outcomes after Surgical Remission of Endogenous Hypercortisolism: a Prospective Cohort Study
Shireen R Chacko, Shubhangi Sharma Sharma, Sarina Ahmadian, et al.
BMJ Open
|
December 18, 2019
Association between hyperlipidemia and mortality after incident acute myocardial infarction or acute decompensated heart failure: a propensity score matched cohort study and a meta-analysis
Mohammed Yousufuddin, Paul Y Takahashi, Brittny Major, et al.
Journal of Clinical Lipidology
|
May 22, 2016
Alirocumab in patients with heterozygous familial hypercholesterolemia undergoing lipoprotein apheresis: Rationale and design of the ODYSSEY ESCAPE trial
Patrick M Moriarty, Klaus G Parhofer, Stephan P Babirak, et al.
Mayo Clinic Proceedings
|
August 19, 2014
A summary and critical assessment of the 2013 ACC/AHA guideline on the treatment of blood cholesterol to reduce atherosclerotic cardiovascular disease risk in adults: filling the gaps
Francisco Lopez-Jimenez, Vinaya Simha, Randal J Thomas, et al.
European Heart Journal
|
August 31, 2016
Alirocumab in patients with heterozygous familial hypercholesterolaemia undergoing lipoprotein apheresis: the ODYSSEY ESCAPE trial
Patrick M Moriarty, Klaus G Parhofer, Stephan P Babirak, et al.
The Journal of Clinical Investigation
|
November 4, 2025
A recurrent ACAA2 variant causes a dominant syndrome of lipodystrophy, lipomatosis, infantile steatohepatitis, and hypoglycemia
Vinaya Simha, Mary Kate LoPiccolo, Anna Platt, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 15, 2003
Phenotypic and genetic heterogeneity in congenital generalized lipodystrophy
Anil K Agarwal, Vinaya Simha, Elif Arioglu Oral, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 63) with videos related to
Sort By:
Page
of 7
The Journal of Clinical Endocrinology and Metabolism
|
October 6, 2021
Impaired Muscle Mitochondrial Function in Familial Partial Lipodystrophy
Vinaya Simha, Ian R Lanza, Surendra Dasari, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 13, 2024
High LDL Particle and APOB Concentrations in Patients With Adrenal Cortical Adenomas
Rashi Sandooja, Jasmine Saini, Annop Kittithaworn, et al.
The New England Journal of Medicine
|
February 22, 2002
Leptin-replacement therapy for lipodystrophy
Elif Arioglu Oral, Vinaya Simha, Elaine Ruiz, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 30, 2025
Cardiometabolic Outcomes after Surgical Remission of Endogenous Hypercortisolism: a Prospective Cohort Study
Shireen R Chacko, Shubhangi Sharma Sharma, Sarina Ahmadian, et al.
BMJ Open
|
December 18, 2019
Association between hyperlipidemia and mortality after incident acute myocardial infarction or acute decompensated heart failure: a propensity score matched cohort study and a meta-analysis
Mohammed Yousufuddin, Paul Y Takahashi, Brittny Major, et al.
Journal of Clinical Lipidology
|
May 22, 2016
Alirocumab in patients with heterozygous familial hypercholesterolemia undergoing lipoprotein apheresis: Rationale and design of the ODYSSEY ESCAPE trial
Patrick M Moriarty, Klaus G Parhofer, Stephan P Babirak, et al.
Mayo Clinic Proceedings
|
August 19, 2014
A summary and critical assessment of the 2013 ACC/AHA guideline on the treatment of blood cholesterol to reduce atherosclerotic cardiovascular disease risk in adults: filling the gaps
Francisco Lopez-Jimenez, Vinaya Simha, Randal J Thomas, et al.
European Heart Journal
|
August 31, 2016
Alirocumab in patients with heterozygous familial hypercholesterolaemia undergoing lipoprotein apheresis: the ODYSSEY ESCAPE trial
Patrick M Moriarty, Klaus G Parhofer, Stephan P Babirak, et al.
The Journal of Clinical Investigation
|
November 4, 2025
A recurrent ACAA2 variant causes a dominant syndrome of lipodystrophy, lipomatosis, infantile steatohepatitis, and hypoglycemia
Vinaya Simha, Mary Kate LoPiccolo, Anna Platt, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 15, 2003
Phenotypic and genetic heterogeneity in congenital generalized lipodystrophy
Anil K Agarwal, Vinaya Simha, Elif Arioglu Oral, et al.
Page
of 7