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62 results

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Page 1
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: de toni t. 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
Growth hormone secretory pattern in non-obese children and adolescents with Prader-Willi syndrome.
Grugni G, Crinò A, Pagani S, Meazza C, Buzi F, De Toni T, Gargantini L, Pilotta A, Pozzan GB, Radetti G, Ragusa L, Salvatoni A, Sartorio A, Bozzola M; Genetic Obesity Study Group, Italian Society of Pediatric Endocrinology and Diabetology. Grugni G, et al. Among authors: de toni t. J Pediatr Endocrinol Metab. 2011;24(7-8):477-81. doi: 10.1515/jpem.2011.269. J Pediatr Endocrinol Metab. 2011. PMID: 21932585
[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: de toni t. Ann Ist Super Sanita. 1999;35(2):221-32. Ann Ist Super Sanita. 1999. PMID: 10645655 Review. Italian.
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: de toni t. 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
[Treatment of adiposity in Prader-Labhart-Willi syndrome].
Naselli A, Vignolo M, Di Battista E, de Toni T, Aicardi G. Naselli A, et al. Among authors: de toni t. Minerva Pediatr. 1983 Jun 15;35(11):579-85. Minerva Pediatr. 1983. PMID: 6621511 Italian. No abstract available.
[Diastrophic dysplasia. Description of a case in early infancy].
Naselli A, Di Battista E, Vignolo M, de Toni T, Tomà P, Aicardi G. Naselli A, et al. Among authors: de toni t. Minerva Pediatr. 1983 Sep 30;35(18):891-7. Minerva Pediatr. 1983. PMID: 6656727 Italian. No abstract available.
Fontaine-Farriaux craniosynostosis: second report in the literature.
Priolo M, De Toni T, Baffico M, Cama A, Seri M, Cusano R, Costabello L, Fondelli P, Capra V, Silengo M, Ravazzolo R, Lerone M. Priolo M, et al. Among authors: de toni t. Am J Med Genet. 2001 May 1;100(3):214-8. Am J Med Genet. 2001. PMID: 11343306
62 results