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Appropriate management of growth hormone deficiency during the age of transition: an Italian Delphi consensus statement.
Cannavò S, Cappa M, Ferone D, Isidori AM, Loche S, Salerno M, Maghnie M; Delphi panel members (paediatric, adult endocrinologists). Cannavò S, et al. Among authors: salerno m. J Endocrinol Invest. 2023 Jan;46(1):189-200. doi: 10.1007/s40618-022-01880-w. Epub 2022 Aug 12. J Endocrinol Invest. 2023. PMID: 35960476 No abstract available.
The cardiovascular risk of GH-deficient adolescents.
Colao A, Di Somma C, Salerno M, Spinelli L, Orio F, Lombardi G. Colao A, et al. Among authors: salerno m. J Clin Endocrinol Metab. 2002 Aug;87(8):3650-5. doi: 10.1210/jcem.87.8.8777. J Clin Endocrinol Metab. 2002. PMID: 12161490
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: salerno m. J Endocrinol Invest. 2007 Feb;30(2):97-103. doi: 10.1007/BF03347406. J Endocrinol Invest. 2007. PMID: 17392598
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 growth hormone-insulin-like growth factor axis in glycogen storage disease type 1: evidence of different growth patterns and insulin-like growth factor levels in patients with glycogen storage disease type 1a and 1b.
Melis D, Pivonello R, Parenti G, Della Casa R, Salerno M, Balivo F, Piccolo P, Di Somma C, Colao A, Andria G. Melis D, et al. Among authors: salerno m. J Pediatr. 2010 Apr;156(4):663-70.e1. doi: 10.1016/j.jpeds.2009.10.032. Epub 2009 Dec 21. J Pediatr. 2010. PMID: 20022338
Screening for mutations in the ISL1 gene in patients with thyroid dysgenesis.
Ferrara AM, Rossi G, Zampella E, Di Candia S, Pagliara V, Nettore IC, Capalbo D, De Sanctis L, Baserga M, Salerno MC, Fenzi G, Macchia PE. Ferrara AM, et al. Among authors: salerno mc. J Endocrinol Invest. 2011 Jul-Aug;34(7):e149-52. doi: 10.3275/7331. Epub 2010 Nov 8. J Endocrinol Invest. 2011. PMID: 21060249
The Italian screening program for primary congenital hypothyroidism: actions to improve screening, diagnosis, follow-up, and surveillance.
Cassio A, Corbetta C, Antonozzi I, Calaciura F, Caruso U, Cesaretti G, Gastaldi R, Medda E, Mosca F, Pasquini E, Salerno MC, Stoppioni V, Tonacchera M, Weber G, Olivieri A; Italian Society for Pediatric Endocrinology and Diabetology; Italian Society for the Study of Metabolic Diseases and Neonatal Screening; Italian National Institute of Health; Italian National Coordinating Group for Congenital Hypothyroidism; Italian Thyroid Association; Italian Society of Pediatrics; Italian Society of Neonatology; Italian Society of Endocrinology; Associazione Medici Endocrinologi. Cassio A, et al. Among authors: salerno mc. J Endocrinol Invest. 2013 Mar;36(3):195-203. doi: 10.3275/8849. Epub 2013 Feb 12. J Endocrinol Invest. 2013. PMID: 23404215 Review.
981 results