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AMRIT BHANGOO, MD
MD
Pediatric Endocrinology Physician
NPI: 1982882254Individual
Specialties, Licenses & Credentials
Pediatric Endocrinology PhysicianPrimary
Pediatrics — Pediatric Endocrinology
Code: 2080P0205X
A119707(CA)
Research & Publications (13)
The genetics of idiopathic hypogonadotropic hypogonadism:unraveling the biology of human sexual development.
PMID 19396025·Pediatr Endocrinol Rev·2009
6-review
Resting energy expenditure in insulin resistance falls with decompensation of insulin secretion in obese children.
PMID 18556967·J Pediatr Endocrinol Metab·2008
2-rct
Novel mutation in cytochrome P450c17 causes complete combined 17alpha-hydroxylase/17,20-lyase deficiency.
PMID 18422032·J Pediatr Endocrinol Metab·2008
5-case
Characterization of insulin resistance syndrome in children and young adults. When to screen for prediabetes?
PMID 18038708·J Pediatr Endocrinol Metab·2007
8-other
Roles of the LHX3 and LHX4 LIM-homeodomain factors in pituitary development.
PMID 17210222·Mol Cell Endocrinol·2007
6-review
Role of a founder c.201_202delCT mutation and new phenotypic features of congenital lipoid adrenal hyperplasia in Palestinians.
PMID 17666473·J Clin Endocrinol Metab·2007
8-other
Phenotypic features of 46, XX females with StAR protein mutations.
PMID 18084157·Pediatr Endocrinol Rev·2007
6-review
Effect of metformin and rosiglitazone in a prepubertal boy with Alström syndrome.
PMID 18038714·J Pediatr Endocrinol Metab·2007
5-case
An intronic growth hormone receptor mutation causing activation of a pseudoexon is associated with a broad spectrum of growth hormone insensitivity phenotypes.
PMID 17148568·J Clin Endocrinol Metab·2007
8-other
Phenotypic variations in lipoid congenital adrenal hyperplasia.
PMID 16639391·Pediatr Endocrinol Rev·2006
7-preclinical
Clinical case seminar: a novel LHX3 mutation presenting as combined pituitary hormonal deficiency.
PMID 16394081·J Clin Endocrinol Metab·2006
5-case
Donor splice mutation in the 11beta-hydroxylase (CypllB1) gene resulting in sex reversal: a case report and review of the literature.
PMID 17172090·J Pediatr Endocrinol Metab·2006
5-case
Phenotypic features associated with mutations in steroidogenic acute regulatory protein.
PMID 16118340·J Clin Endocrinol Metab·2005
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2650 ELM AVE, SUITE 210
LONG BEACH, CA 90806 - Phone
- (562) 595-0166
Quick Facts
- NPI
- 1982882254
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 13
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