Sneha Arya
Mumbai, MH, India
Last Updated: 09/26/2026
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Found 26 publications
46, XY under-virilization and NR5A1 variants: Monocentric Indian experience and systematic review.
Journal: Annales d'endocrinologie
Published: October 17, 2024
Genotype and Phenotype of 21-Hydroxylase Deficiency: A Single Center Experience from Western India.
Journal: Indian pediatrics
Published: July 25, 2024
LHCGR inactivating variants: single center experience and systematic review of phenotype-genotype of 46,XY and 46,XX patients.
Journal: Endocrine connections
Published: May 22, 2024
Steroidogenic acute regulatory protein (STAR) deficiency: Our experience and systematic review for phenotype-genotype correlation.
Journal: Clinical endocrinology
Published: September 23, 2023
Hereditary Hypophosphatemic Rickets with Hypercalciuria Presenting with Enthesopathy, Renal Cysts, and High Serum c-Terminal FGF23: Single-Center Experience and Systematic Review.
Journal: Calcified tissue international
Published: August 01, 2023
46,XX aromatase deficiency: A single-center experience with the varied spectrum and recurrent variants, and a systematic review of hormonal parameters.
Journal: Annales d'endocrinologie
Published: February 25, 2023
Genotypic Spectrum and its Correlation with Alopecia and Clinical Response in Hereditary Vitamin D Resistant Rickets: Our Experience and Systematic Review.
Journal: Calcified tissue international
Published: November 07, 2022
Pediatric Macrocorticotropinoma: Do They Differ from Microcorticotropinoma?
Journal: Neuroendocrinology
Published: October 04, 2022
Side-chain cleavage enzyme deficiency: Systematic review and case series.
Journal: Clinical endocrinology
Published: August 03, 2022
Genetic spectrum of Kallmann syndrome: Single-center experience and systematic review.
Journal: Clinical endocrinology
Published: June 27, 2022
Last Updated: 09/26/2026