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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|June 29, 2006
Analysis of bone mineral density and turnover in patients with cystic fibrosis: associations between the IGF system and inflammatory cytokinesMaria E Street, Cinzia Spaggiari, Maria A Ziveri, 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.Bone|February 14, 2006
Cross-sectional reference data for phalangeal quantitative ultrasound from early childhood to young-adulthood according to gender, age, skeletal growth, and pubertal developmentGiampiero I Baroncelli, Giovanni Federico, Marina Vignolo, et al.Bone|September 24, 2009
Analysis of quantitative ultrasound graphic trace and derived variables assessed at proximal phalanges of the hand in healthy subjects and in patients with cerebral palsy or juvenile idiopathic arthritis. A pilot studyGiampiero I Baroncelli, Roberta Battini, Silvano Bertelloni, 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.Pageof 5