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Calcified Tissue International|May 14, 2022
Genotype-Phenotype Correlations in Asian Indian Children and Adolescents with Primary HyperparathyroidismAnima Sharma, Saba Memon, Anurag R Lila, et al.Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|August 1, 2021
Clinical, Hormonal, Genetic, and Molecular Characteristics in Androgen Insensitivity Syndrome in an Asian Indian Cohort from a Single Centre in Western IndiaSneha Arya, Rohit Barnabas, Anurag Ranjan Lila, et al.Indian Pediatrics|July 25, 2024
Genotype and Phenotype of 21-Hydroxylase Deficiency: A Single Center Experience from Western IndiaManjiri Karlekar, Rohit Barnabas, Vijaya Sarathi, et al.Neuroendocrinology|December 19, 2021
GNRH1 Variants in Congenital Hypogonadotropic Hypogonadism: Single-Center Experience and Systematic Literature ReviewVirendra A Patil, Anurag Ranjan Lila, Nalini Shah, et al.Clinical Endocrinology|December 4, 2020
Expanding genetic spectrum and discriminatory role of steroid profiling by LC-MS/MS in 11β-hydroxylase deficiencyManjiri Pramod Karlekar, Vijaya Sarathi, Anurag Lila, et al.Pituitary|March 20, 2021
POU1F1 mutations in combined pituitary hormone deficiency: differing spectrum of mutations in a Western-Indian cohort and systematic analysis of world literatureSwati Jadhav, Chakra Diwaker, Anurag R Lila, et al.Clinical Endocrinology|February 16, 2022
17β hydroxysteroid dehydrogenase 3 deficiency in 46,XY disorders of sex development: Our experience and a gender role-focused systematic reviewBrijesh Krishnappa, Sneha Arya, Anurag R Lila, et al.Endocrine Connections|August 20, 2024
LHCGR inactivating variants: single center experience and systematic review of phenotype-genotype of 46,XY and 46,XX patientsRohit Barnabas, Swati Jadhav, Anurag Ranjan Lila, et al.Endocrine Connections|November 29, 2017
Phenotype-genotype spectrum of AAA syndrome from Western India and systematic review of literatureHiren Patt, Katrin Koehler, Sailesh Lodha, et al.Journal of the Endocrine Society|February 18, 2022
17α-Hydroxylase/17,20-Lyase Deficiency in 46,XY: Our Experience and Review of LiteratureMadhur Maheshwari, Sneha Arya, Anurag Ranjan Lila, et al.Pageof 3