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Real-life long-term efficacy and safety of recombinant human growth hormone therapy in children with short stature homeobox-containing deficiency. in Endocrine connections / Endocr Connect. 2023 Jun 8;12(7):e220402. doi: 10.1530/EC-22-0402. Print 2023 Jul 1.
2023
AOU Alessandria

Bruzzi P; Vannelli S; Scarano E; Di Iorgi N; Parpagnoli M; Salerno M; Pitea M; Elisabeth Street M; Secco A; Andrea Trettene A; Wasniewska M; Corciulo N; Tornese G; Felicia Faienza M; Delvecchio M; Filomena Madeo S; Iughetti L;

Novel Pathogenetic Variants in PTHLH and TRPS1 Genes Causing Syndromic Brachydactyly. in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research / J Bone Miner Res. 2022 Mar;37(3):465-474. doi: 10.1002/jbmr.4490. Epub 2022 Jan 17.
2022
AOU Alessandria

Elli FM; Mattinzoli D; Lucca C; Piu M; Maffini MA; Costanza J; Fontana L; Santaniello C; Forino C; Milani D; Bonati MT; Secco A; Gastaldi R; Alfieri C; Messa P; Miozzo M; Arosio M; Mantovani G;

Copy number variations residing outside the SHOX enhancer region are involved in Short Stature and Léri-Weill dyschondrosteosis. in Molecular genetics & genomic medicine / Mol Genet Genomic Med. 2022 Jan;10(1):e1793. doi: 10.1002/mgg3.1793. Epub 2021 Nov 23.
2022
AOU Alessandria
AOU Città della Salute di Torino

Giordano M; Bellone S; Prodam F; Follenzi A; Secco A; Al Essa W; Cucci A; Monzani A; Babu D; Mellone S; Vannelli S; Fanelli A;