Lipodystrophies: Genetic and Acquired Body Fat Disorders

od Garg, Abhimanyu
Wydane w J Clin Endocrinol Metab (2011)

LIPODYSTROPHY SYNDROMES

od Hussain, Iram, Garg, Abhimanyu
Wydane w Dermatol Clin (2008)

MON-695 Multiple Recurrent Lipomatoses with Thiazolidinedione Therapy in Familial Partial Lipodystrophy, Dunnigan Variety (FPLD2)

od Patni, Nivedita, Garg, Abhimanyu
Wydane w J Endocr Soc (2020)

Lipodystrophy Syndromes

od Hussain, Iram, Garg, Abhimanyu
Wydane w Endocrinol Metab Clin North Am (2016)

De Novo Heterozygous FBN1 Mutations in the Extreme C-Terminal Region Cause Progeroid Fibrillinopathy

od Garg, Abhimanyu, Xing, Chao
Wydane w Am J Med Genet A (2014)

Congenital generalized lipodystrophies—new insights into metabolic dysfunction

od Patni, Nivedita, Garg, Abhimanyu
Wydane w Nat Rev Endocrinol (2015)

Severe Liver Injury Associated With High-Dose Atorvastatin Therapy

od Saha, Amit, Garg, Abhimanyu
Wydane w J Investig Med High Impact Case Rep (2021)

Caveolin-1: A New Locus for Human Lipodystrophy

od Garg, Abhimanyu, Agarwal, Anil K.
Wydane 2008

Lipodystrophies: Disorders of adipose tissue biology

od Garg, Abhimanyu, Agarwal, Anil K.
Wydane 2009

Enzymatic activity of the human 1-acylglycerol-3-phosphate-O-acyltransferase isoform 11: upregulated in breast and cervical cancers

od Agarwal, Anil K., Garg, Abhimanyu
Wydane 2010

Overlapping syndrome with Familial Partial Lipodystrophy, Dunnigan variety and Cardiomyopathy due to Amino-terminal Heterozygous Missense lamin A/C Mutations

od Subramanyam, Lalitha, Simha, Vinaya, Garg, Abhimanyu
Wydane 2009

Type 1 Hyperlipoproteinemia Due to Compound Heterozygous Rare Variants in GCKR

od Shetty, Shilpa, Xing, Chao, Garg, Abhimanyu
Wydane w J Clin Endocrinol Metab (2016)

A Heterozygous Null LDLR Mutation in a Familial Hypercholesterolemia Patient with an Atypical Presentation due to Alcohol Abuse

od Panach, Kamaldeep, Garg, Abhimanyu, Ahmad, Zahid
Wydane w Circ Cardiovasc Genet (2017)

Postmortem Findings in a Young Man With Congenital Generalized Lipodystrophy, Type 4 Due to CAVIN1 Mutations

od Patni, Nivedita, Vuitch, Frank, Garg, Abhimanyu
Wydane w J Clin Endocrinol Metab (2018)

Lipodystrophies, dyslipidaemias and atherosclerotic vascular disease

od Hussain, Iram, Patni, Nivedita, Garg, Abhimanyu
Wydane w Pathology (2018)

Orlistat Therapy for Children With Type 1 Hyperlipoproteinemia: A Randomized Clinical Trial

od Patni, Nivedita, Quittner, Claudia, Garg, Abhimanyu
Wydane w J Clin Endocrinol Metab (2018)

Novel Heterozygous LMNA Variants Causing Familial Partial Lipodystrophy, Dunnigan Variety

od Wadhwa, Akhilesh, Vasandani, Chandna, Garg, Abhimanyu
Wydane w J Endocr Soc (2021)

Diet-Responsive Hypercholesterolemia With Cardiofaciocutaneous Syndrome Type 3

od Patni, Nivedita, Garg, Abhimanyu, Xing, Chao
Wydane w J Endocr Soc (2021)

Mislocalization of prelamin A Tyr646Phe mutant to the nuclear pore complex in human embryonic kidney 293 cells

od Pan, Yong, Garg, Abhimanyu, Agarwal, Anil K.
Wydane 2007

Enzymatic activities of the human AGPAT isoform 3 and isoform 5: localization of AGPAT5 to mitochondria

od Prasad, Sneha S., Garg, Abhimanyu, Agarwal, Anil K.
Wydane 2011