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Page 1
Disorders of glucose metabolism in Prader-Willi syndrome: Results of a multicenter Italian cohort study.
Fintini D, Grugni G, Bocchini S, Brufani C, Di Candia S, Corrias A, Delvecchio M, Salvatoni A, Ragusa L, Greggio N, Franzese A, Scarano E, Trifirò G, Mazzanti L, Chiumello G, Cappa M, Crinò A; Genetic Obesity Study Group of the Italian Society of Pediatric Endocrinology and Diabetology (ISPED). Fintini D, et al. Among authors: salvatoni a. Nutr Metab Cardiovasc Dis. 2016 Sep;26(9):842-7. doi: 10.1016/j.numecd.2016.05.010. Epub 2016 Jun 3. Nutr Metab Cardiovasc Dis. 2016. PMID: 27381990
[Prader-Willi syndrome].
Beccaria L, Bosio L, Benzi F, Bregani P, Achutegui I, Chiumello G, Livieri C, Trifirò G, de Toni T, Iughetti L, Ragusa L, Salvatoni A, Tonini G, Corrias A, Crinò A. Beccaria L, et al. Among authors: salvatoni a. Ann Ist Super Sanita. 1999;35(2):221-32. Ann Ist Super Sanita. 1999. PMID: 10645655 Review. Italian.
GH/IGF-I axis in Prader-Willi syndrome: evaluation of IGF-I levels and of the somatotroph responsiveness to various provocative stimuli. Genetic Obesity Study Group of Italian Society of Pediatric Endocrinology and Diabetology.
Corrias A, Bellone J, Beccaria L, Bosio L, Trifirò G, Livieri C, Ragusa L, Salvatoni A, Andreo M, Ciampalini P, Tonini G, Crinò A. Corrias A, et al. Among authors: salvatoni a. J Endocrinol Invest. 2000 Feb;23(2):84-9. doi: 10.1007/BF03343684. J Endocrinol Invest. 2000. PMID: 10800760 Clinical Trial.
Hypogonadism and pubertal development in Prader-Willi syndrome.
Crinò A, Schiaffini R, Ciampalini P, Spera S, Beccaria L, Benzi F, Bosio L, Corrias A, Gargantini L, Salvatoni A, Tonini G, Trifirò G, Livieri C; Genetic Obesity Study Group of Italian Society of Pediatric endocrinology and diabetology (SIEDP). Crinò A, et al. Among authors: salvatoni a. Eur J Pediatr. 2003 May;162(5):327-33. doi: 10.1007/s00431-002-1132-4. Epub 2003 Feb 27. Eur J Pediatr. 2003. PMID: 12692714
The Italian National Survey for Prader-Willi syndrome: an epidemiologic study.
Grugni G, Crinò A, Bosio L, Corrias A, Cuttini M, De Toni T, Di Battista E, Franzese A, Gargantini L, Greggio N, Iughetti L, Livieri C, Naselli A, Pagano C, Pozzan G, Ragusa L, Salvatoni A, Trifirò G, Beccaria L, Bellizzi M, Bellone J, Brunani A, Cappa M, Caselli G, Cerioni V, Delvecchio M, Giardino D, Iannì F, Memo L, Pilotta A, Pomara C, Radetti G, Sacco M, Sanzari A, Sartorio A, Tonini G, Vettor R, Zaglia F, Chiumello G; Genetic Obesity Study Group of Italian Society of Pediatric Endocrinology and Diabetology (ISPED). Grugni G, et al. Among authors: salvatoni a. Am J Med Genet A. 2008 Apr 1;146A(7):861-72. doi: 10.1002/ajmg.a.32133. Am J Med Genet A. 2008. PMID: 18203198
Prevalence of pathogenetic MC4R mutations in Italian children with early onset obesity, tall stature and familial history of obesity.
Santoro N, Cirillo G, Xiang Z, Tanas R, Greggio N, Morino G, Iughetti L, Vottero A, Salvatoni A, Di Pietro M, Balsamo A, Crinò A, Grandone A, Haskell-Luevano C, Perrone L, del Giudice EM. Santoro N, et al. Among authors: salvatoni a. BMC Med Genet. 2009 Mar 12;10:25. doi: 10.1186/1471-2350-10-25. BMC Med Genet. 2009. PMID: 19284607 Free PMC article.
A survey on Prader-Willi syndrome in the Italian population: prevalence of historical and clinical signs.
Crinò A, Di Giorgio G, Livieri C, Grugni G, Beccaria L, Bosio L, Corrias A, Chiumello G, Trifirò G, Salvatoni A, Tonini G, Gargantini L, de Toni T, Valerio G, Ragusa L, Franzese A, Rinaldi MM, Spera S, Gattinara GC, Villani S, Iughetti L; Genetic Obesity Study Group; Italian Society of Pediatric Endocrinology and Diabetology. Crinò A, et al. Among authors: salvatoni a. J Pediatr Endocrinol Metab. 2009 Oct;22(10):883-93. doi: 10.1515/jpem.2009.22.10.883. J Pediatr Endocrinol Metab. 2009. PMID: 20020576
98 results