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Profile
Sunil Sinha
Assistant Clinical Professor, Pediatrics - (Clinical Series Track)
Pediatrics
Full Page
Overview
Research
More
Publications
(15)
Recent
Endocrinopathies Associated With Noonan Syndrome
2019
endocrinopathies,
noonan syndrome,
genetic disorders,
hormonal imbalance,
pediatric endocrinology
Experience with cinacalcet in familial hypocalciuric hypercalcemia resulting from inactivating mutations in calcium sensing receptor CaSR)
2018
familial hypocalciuric hypercalcemia,
cinacalcet,
casr mutations,
calcium sensing receptor,
inactivating mutations
Altered glucose disposition and insulin sensitivity in peri-pubertal first-degree relatives of women with polycystic ovary syndrome
2012
Phenotypic Variation of SF1 Gene Mutations
2011
Leydig Cell Hypoplasia due to Inactivating Luteinizing Hormone/Chorionic Gonadotropin Receptor Gene Mutation Presenting as a 46,XY DSD
2011
Inguinal Hernia in a Phenotypic Female Infant May Reveal a 46XY Sex Reversal, Supported by the Identification of a Novel SF1 Gene Mutation
2011
Endothelial Function as Measured by Peripheral Arterial Tonometry Increases during Pubertal Advancement
2011
Isolated mild clitoral hypertrophy may reveal 46,XY disorders of sex development in infancy due to17βHSD-3defect confirmed by molecular analysis
2011
A Novel Y332C Missense Mutation in the Intracellular Domain of The Human Growth Hormone Receptor Does Not Alter STAT5b Signaling: Redundancy of GHR Intracellular Tyrosines Involved in STAT5b Signaling
2011
Expanding the Spectrum of Mutations inGH1andGHRHR: Genetic Screening in a Large Cohort of Patients with Congenital Isolated Growth Hormone Deficiency
2009
