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Page 1
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: salerno m. 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
Improvement of cardiac performance and cardiovascular risk factors in children with GH deficiency after two years of GH replacement therapy: an observational, open, prospective, case-control study.
Salerno M, Esposito V, Farina V, Radetti G, Umbaldo A, Capalbo D, Spinelli L, Muzzica S, Lombardi G, Colao A. Salerno M, et al. J Clin Endocrinol Metab. 2006 Apr;91(4):1288-95. doi: 10.1210/jc.2005-0981. Epub 2006 Jan 10. J Clin Endocrinol Metab. 2006. PMID: 16403823 Clinical Trial.
Cut-off limits of the GH response to GHRH plus arginine test and IGF-I levels for the diagnosis of GH deficiency in late adolescents and young adults.
Corneli G, Di Somma C, Prodam F, Bellone J, Bellone S, Gasco V, Baldelli R, Rovere S, Schneider HJ, Gargantini L, Gastaldi R, Ghizzoni L, Valle D, Salerno M, Colao A, Bona G, Ghigo E, Maghnie M, Aimaretti G. Corneli G, et al. Among authors: salerno m. Eur J Endocrinol. 2007 Dec;157(6):701-8. doi: 10.1530/EJE-07-0384. Eur J Endocrinol. 2007. PMID: 18057376
The natural history of the normal/mild elevated TSH serum levels in children and adolescents with Hashimoto's thyroiditis and isolated hyperthyrotropinaemia: a 3-year follow-up.
Radetti G, Maselli M, Buzi F, Corrias A, Mussa A, Cambiaso P, Salerno M, Cappa M, Baiocchi M, Gastaldi R, Minerba L, Loche S. Radetti G, et al. Among authors: salerno m. Clin Endocrinol (Oxf). 2012 Mar;76(3):394-8. doi: 10.1111/j.1365-2265.2011.04251.x. Clin Endocrinol (Oxf). 2012. PMID: 21981142
Growth hormone treatment of adolescents with growth hormone deficiency (GHD) during the transition period: results of a survey among adult and paediatric endocrinologists from Italy. Endorsed by SIEDP/ISPED, AME, SIE, SIMA.
Aimaretti G, Attanasio R, Cannavò S, Nicoletti MC, Castello R, Di Somma C, Garofalo P, Iughetti L, Loche S, Maghnie M, Mazzanti L, Saggese G, Salerno M, Tonini G, Toscano V, Zucchini S, Cappa M. Aimaretti G, et al. Among authors: salerno m. J Endocrinol Invest. 2015 Mar;38(3):377-82. doi: 10.1007/s40618-014-0201-7. Epub 2014 Nov 2. J Endocrinol Invest. 2015. PMID: 25362629
Early-onset central diabetes insipidus is associated with de novo arginine vasopressin-neurophysin II or Wolfram syndrome 1 gene mutations.
Perrotta S, Di Iorgi N, Ragione FD, Scianguetta S, Borriello A, Allegri AE, Ferraro M, Santoro C, Napoli F, Calcagno A, Giaccardi M, Cappa M, Salerno MC, Cozzolino D, Maghnie M. Perrotta S, et al. Among authors: salerno mc. Eur J Endocrinol. 2015 Apr;172(4):461-72. doi: 10.1530/EJE-14-0942. Eur J Endocrinol. 2015. PMID: 25740874
1,018 results