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MRS. ANITA AGARWAL M.D.
M.D.
Internal Medicine Physician
NPI: 1649293226IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
12612737-1205(TX)V5228(TX)
Education
OTHER
Class of 1997
Research & Publications (20)
Severe mandibuloacral dysplasia-associated lipodystrophy and progeria in a young girl with a novel homozygous Arg527Cys LMNA mutation.
PMID 18796515·J Clin Endocrinol Metab·2008
5-case
Functional characterization of human 1-acylglycerol-3-phosphate-O-acyltransferase isoform 9: cloning, tissue distribution, gene structure, and enzymatic activity.
PMID 17535882·J Endocrinol·2007
7-preclinical
Genetic disorders of adipose tissue development, differentiation, and death.
PMID 16722806·Annu Rev Genomics Hum Genet·2006
6-review
Functional characterization of human 1-acylglycerol-3-phosphate acyltransferase isoform 8: cloning, tissue distribution, gene structure, and enzymatic activity.
PMID 16620771·Arch Biochem Biophys·2006
7-preclinical
Focal segmental glomerulosclerosis in patients with mandibuloacral dysplasia owing to ZMPSTE24 deficiency.
PMID 17152860·J Investig Med·2006
5-case
Genetic basis of lipodystrophies and management of metabolic complications.
PMID 16409151·Annu Rev Med·2006
6-review
Minireview: cellular redox state regulates hydroxysteroid dehydrogenase activity and intracellular hormone potency.
PMID 15774561·Endocrinology·2005
6-review
Genetic basis of congenital generalized lipodystrophy.
PMID 14557833·Int J Obes Relat Metab Disord·2004
6-review
Phenotypic and genetic heterogeneity in congenital generalized lipodystrophy.
PMID 14557463·J Clin Endocrinol Metab·2003
8-other
Congenital generalized lipodystrophy: significance of triglyceride biosynthetic pathways.
PMID 12826327·Trends Endocrinol Metab·2003
6-review
Cortisol metabolism and visceral obesity: role of 11beta-hydroxysteroid dehydrogenase type I enzyme and reduced co-factor NADPH.
PMID 14682470·Endocr Res·2003
6-review
Zinc metalloproteinase, ZMPSTE24, is mutated in mandibuloacral dysplasia.
PMID 12913070·Hum Mol Genet·2003
4-observational
AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34.
PMID 11967537·Nat Genet·2002
8-other
A novel heterozygous mutation in peroxisome proliferator-activated receptor-gamma gene in a patient with familial partial lipodystrophy.
PMID 11788685·J Clin Endocrinol Metab·2002
4-observational
Structure of the VPATPD gene encoding subunit D of the human vacuolar proton ATPase.
PMID 11118322·Biochem Biophys Res Commun·2000
7-preclinical
Expression of HSD11K (NAD+ dependent 11beta-hydroxysteroid dehydrogenase) promoter constructs in renal cell lines.
PMID 10921454·Endocr Res·2000
7-preclinical
CA-Repeat polymorphism in intron 1 of HSD11B2 : effects on gene expression and salt sensitivity.
PMID 10948076·Hypertension·2000
3-trial
Sperm viability, apoptosis, and intracellular reactive oxygen species levels in human spermatozoa before and after induction of oxidative stress.
PMID 19100530·Fertil Steril·2010
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 2740 VALWOOD PKWY STE 121
DALLAS, TX 75234 - Phone
- (469) 518-3200
Quick Facts
- NPI
- 1649293226
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 2
- Years in Practice
- 29
- Publications
- 20
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