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Frontiers in Pediatrics|May 10, 2021
Disorders/Differences of Sex Development Presenting in the Newborn With 46,XY KaryotypeSilvano Bertelloni, Nina Tyutyusheva, Margherita Valiani, et al.
Hormone Research in Paediatrics|January 18, 2014
NR5A1 gene mutations: clinical, endocrine and genetic features in two girls with 46,XY disorder of sex developmentSilvano Bertelloni, Eleonora Dati, Fulvia Baldinotti, et al.
Thescientificworldjournal|May 31, 2012
Central precocious puberty: treatment with triptorelin 11.25 mgElena Chiocca, Eleonora Dati, Giampiero I Baroncelli, et al.
Journal of Bone and Mineral Metabolism|August 11, 2020
Pulp chamber features, prevalence of abscesses, disease severity, and PHEX mutation in X-linked hypophosphatemic ricketsGiampiero I Baroncelli, Elisa Zampollo, Mario Manca, et al.
European Journal of Medical Genetics|July 1, 2024
Safety and efficacy of burosumab in improving phosphate metabolism, bone health, and quality of life in adolescents with X-linked hypophosphatemic ricketsGiampiero I Baroncelli, Anna Grandone, Antonio Aversa, et al.
Hormone Research in Paediatrics|February 23, 2018
Novel Familial Variant of the Desert Hedgehog Gene: Clinical Findings in Two Sisters with 46,XY Gonadal Dysgenesis or 46,XX Karyotype and Literature ReviewFulvia Baldinotti, Tiziana Cavallaro, Eleonora Dati, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|April 13, 2016
5α-Reductase-2 Deficiency: Clinical Findings, Endocrine Pitfalls, and Genetic Features in a Large Italian CohortSilvano Bertelloni, Fulvia Baldinotti, Gianni Russo, et al.
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