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The Journal of Clinical Endocrinology and Metabolism
|
November 7, 2003
Phenotypic heterogeneity in body fat distribution in patients with congenital generalized lipodystrophy caused by mutations in the AGPAT2 or seipin genes
Vinaya Simha, Abhimanyu Garg
American Journal of Medical Genetics. Part A
|
March 26, 2014
De novo heterozygous FBN1 mutations in the extreme C-terminal region cause progeroid fibrillinopathy
Abhimanyu Garg, Chao Xing
Archives of Internal Medicine
|
June 15, 2011
Lack of cardiovascular disease among old order amish with familial defective apolipoprotein B
Zahid Ahmad, Abhimanyu Garg
Current Opinion in Lipidology
|
March 15, 2006
Lipodystrophy: lessons in lipid and energy metabolism
Vinaya Simha, Abhimanyu Garg
Endocrinology and Metabolism Clinics of North America
|
November 9, 2016
Lipodystrophy Syndromes
Iram Hussain, Abhimanyu Garg
Journal of Clinical Lipidology
|
November 13, 2024
Complex dyslipidemia induced by lorlatinib therapy: A case study
Julianna West, Abhimanyu Garg
Current Opinion in Lipidology
|
June 5, 2009
Inherited lipodystrophies and hypertriglyceridemia
Vinaya Simha, Abhimanyu Garg
The Journal of Clinical Endocrinology and Metabolism
|
February 12, 2002
Body fat distribution and metabolic derangements in patients with familial partial lipodystrophy associated with mandibuloacral dysplasia
Vinaya Simha, Abhimanyu Garg
Journal of Clinical Lipidology
|
December 22, 2015
Marked lowering of high-density lipoprotein cholesterol levels due to high dose bexarotene therapy
Samata Basani, Abhimanyu Garg
Medicine
|
March 18, 2003
Clinical features and metabolic derangements in acquired generalized lipodystrophy: case reports and review of the literature
Anoop Misra, Abhimanyu Garg
Page
of 19
Search research articles
Search
Showing results (11-20 of 181) with videos related to
Sort By:
Page
of 19
The Journal of Clinical Endocrinology and Metabolism
|
November 7, 2003
Phenotypic heterogeneity in body fat distribution in patients with congenital generalized lipodystrophy caused by mutations in the AGPAT2 or seipin genes
Vinaya Simha, Abhimanyu Garg
American Journal of Medical Genetics. Part A
|
March 26, 2014
De novo heterozygous FBN1 mutations in the extreme C-terminal region cause progeroid fibrillinopathy
Abhimanyu Garg, Chao Xing
Archives of Internal Medicine
|
June 15, 2011
Lack of cardiovascular disease among old order amish with familial defective apolipoprotein B
Zahid Ahmad, Abhimanyu Garg
Current Opinion in Lipidology
|
March 15, 2006
Lipodystrophy: lessons in lipid and energy metabolism
Vinaya Simha, Abhimanyu Garg
Endocrinology and Metabolism Clinics of North America
|
November 9, 2016
Lipodystrophy Syndromes
Iram Hussain, Abhimanyu Garg
Journal of Clinical Lipidology
|
November 13, 2024
Complex dyslipidemia induced by lorlatinib therapy: A case study
Julianna West, Abhimanyu Garg
Current Opinion in Lipidology
|
June 5, 2009
Inherited lipodystrophies and hypertriglyceridemia
Vinaya Simha, Abhimanyu Garg
The Journal of Clinical Endocrinology and Metabolism
|
February 12, 2002
Body fat distribution and metabolic derangements in patients with familial partial lipodystrophy associated with mandibuloacral dysplasia
Vinaya Simha, Abhimanyu Garg
Journal of Clinical Lipidology
|
December 22, 2015
Marked lowering of high-density lipoprotein cholesterol levels due to high dose bexarotene therapy
Samata Basani, Abhimanyu Garg
Medicine
|
March 18, 2003
Clinical features and metabolic derangements in acquired generalized lipodystrophy: case reports and review of the literature
Anoop Misra, Abhimanyu Garg
Page
of 19