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2002 2
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Page 1
Complete Androgen Insensitivity Syndrome: From Bench to Bed.
Tyutyusheva N, Mancini I, Baroncelli GI, D'Elios S, Peroni D, Meriggiola MC, Bertelloni S. Tyutyusheva N, et al. Among authors: baroncelli gi. Int J Mol Sci. 2021 Jan 27;22(3):1264. doi: 10.3390/ijms22031264. Int J Mol Sci. 2021. PMID: 33514065 Free PMC article. Review.
Puberty and bone development.
Saggese G, Baroncelli GI, Bertelloni S. Saggese G, et al. Among authors: baroncelli gi. Best Pract Res Clin Endocrinol Metab. 2002 Mar;16(1):53-64. doi: 10.1053/beem.2001.0180. Best Pract Res Clin Endocrinol Metab. 2002. PMID: 11987898 Review.
Vitamin D deficiency.
Baroncelli GI. Baroncelli GI. N Engl J Med. 2007 Nov 8;357(19):1981; author reply 1981-2. N Engl J Med. 2007. PMID: 17992734 No abstract available.
Molecular analysis of the GNAS1 gene for the correct diagnosis of Albright hereditary osteodystrophy and pseudohypoparathyroidism.
De Sanctis L, Romagnolo D, Olivero M, Buzi F, Maghnie M, Scirè G, Crino A, Baroncelli GI, Salerno M, Di Maio S, Cappa M, Grosso S, Rigon F, Lala R, De Sanctis C, Dianzani I. De Sanctis L, et al. Among authors: baroncelli gi. Pediatr Res. 2003 May;53(5):749-55. doi: 10.1203/01.PDR.0000059752.07086.A2. Epub 2003 Mar 5. Pediatr Res. 2003. PMID: 12621129
14 results