Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Journal of Endocrinological Investigation|November 10, 2010
Screening for mutations in the ISL1 gene in patients with thyroid dysgenesisA M Ferrara, G Rossi, E Zampella, et al.
Journal of Endocrinological Investigation|February 20, 2024
Transition from pediatric to adult care in patients with Turner syndrome in Italy: a consensus statement by the TRAMITI projectT Aversa, L De Sanctis, M F Faienza, et al.
Italian Journal of Pediatrics|June 2, 2019
X-linked hypophosphatemic rickets: an Italian experts' opinion surveyF Emma, M Cappa, F Antoniazzi, et al.
Journal of Endocrinological Investigation|May 18, 2021
Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patientsS Garelli, M Dalla Costa, C Sabbadin, et al.
Nature Genetics|September 2, 1999
Non-type I cystinuria caused by mutations in SLC7A9, encoding a subunit (bo,+AT) of rBATL Feliubadaló, M Font, J Purroy, et al.
Endocrine Connections|November 6, 2023
Development of a pediatric differentiated thyroid carcinoma registry within the EuRRECa project: rationale and protocolS C Clement, W E Visser, C A Lebbink, et al.
Pageof 4