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Recombinant human GH replacement therapy in children with pseudohypoparathyroidism type Ia: first study on the effect on growth.
Mantovani G, Ferrante E, Giavoli C, Linglart A, Cappa M, Cisternino M, Maghnie M, Ghizzoni L, de Sanctis L, Lania AG, Beck-Peccoz P, Spada A. Mantovani G, et al. Among authors: de sanctis l. J Clin Endocrinol Metab. 2010 Nov;95(11):5011-7. doi: 10.1210/jc.2010-1649. Epub 2010 Aug 18. J Clin Endocrinol Metab. 2010. PMID: 20719837 Clinical Trial.
Growth hormone treatment in irradiated children with brain tumors.
Corrias A, Picco P, Einaudi S, de Sanctis L, Besenzon L, Garrè ML, Brach del Prever A, de Sanctis C. Corrias A, et al. Among authors: de sanctis c, de sanctis l. J Pediatr Endocrinol Metab. 1997 Jan-Feb;10(1):41-9. doi: 10.1515/jpem.1997.10.1.41. J Pediatr Endocrinol Metab. 1997. PMID: 9364341
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: de sanctis c. 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
GH secretion in a cohort of children with pseudohypoparathyroidism type Ia.
de Sanctis L, Bellone J, Salerno M, Faleschini E, Caruso-Nicoletti M, Cicchetti M, Concolino D, Balsamo A, Buzi F, Ghizzoni L, de Sanctis C. de Sanctis L, et al. Among authors: de sanctis c. J Endocrinol Invest. 2007 Feb;30(2):97-103. doi: 10.1007/BF03347406. J Endocrinol Invest. 2007. PMID: 17392598
Pseudohypoparathyroidism and GNAS epigenetic defects: clinical evaluation of albright hereditary osteodystrophy and molecular analysis in 40 patients.
Mantovani G, de Sanctis L, Barbieri AM, Elli FM, Bollati V, Vaira V, Labarile P, Bondioni S, Peverelli E, Lania AG, Beck-Peccoz P, Spada A. Mantovani G, et al. Among authors: de sanctis l. J Clin Endocrinol Metab. 2010 Feb;95(2):651-8. doi: 10.1210/jc.2009-0176. Epub 2010 Jan 8. J Clin Endocrinol Metab. 2010. PMID: 20061437 Free article.
Quantitative analysis of methylation defects and correlation with clinical characteristics in patients with pseudohypoparathyroidism type I and GNAS epigenetic alterations.
Elli FM, de Sanctis L, Bollati V, Tarantini L, Filopanti M, Barbieri AM, Peverelli E, Beck-Peccoz P, Spada A, Mantovani G. Elli FM, et al. Among authors: de sanctis l. J Clin Endocrinol Metab. 2014 Mar;99(3):E508-17. doi: 10.1210/jc.2013-3086. Epub 2013 Jan 1. J Clin Endocrinol Metab. 2014. PMID: 24423294 Free article.
230 results