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Low prevalence of HNF1A mutations after molecular screening of multiple MODY genes in 58 Italian families recruited in the pediatric or adult diabetes clinic from a single Italian hospital.
Delvecchio M, Ludovico O, Menzaghi C, Di Paola R, Zelante L, Marucci A, Grasso V, Trischitta V, Carella M, Barbetti F, Gallo F, Coccioli MS, Zecchino C, Faienza MF, Cardinale G, Franzese A, Mozzillo E, Iafusco D, Zanfardino A. Delvecchio M, et al. Diabetes Care. 2014 Dec;37(12):e258-60. doi: 10.2337/dc14-1788. Diabetes Care. 2014. PMID: 25414397 No abstract available.
Anthropometric characteristics of newborns with Prader-Willi syndrome.
Salvatoni A, Moretti A, Grugni G, Agosti M, Azzolini S, Bonaita V, Cianci P, Corica D, Crinò A, Delvecchio M, Ferraris S, Greggio NA, Iughetti L, Licenziati MR, Madeo SF, Nosetti L, Pajno R, Rutigliano I, Sacco M, Salvatore S, Scarano E, Trifirò G, Wasniewska M. Salvatoni A, et al. Among authors: delvecchio m. Am J Med Genet A. 2019 Oct;179(10):2067-2074. doi: 10.1002/ajmg.a.61304. Epub 2019 Jul 30. Am J Med Genet A. 2019. PMID: 31361394
Anti-pituitary antibodies in children with newly diagnosed celiac disease: a novel finding contributing to linear-growth impairment.
Delvecchio M, De Bellis A, Francavilla R, Rutigliano V, Predieri B, Indrio F, De Venuto D, Sinisi AA, Bizzarro A, Bellastella A, Iughetti L, Cavallo L; Italian Autoimmune Hypophysitis Network Study. Delvecchio M, et al. Am J Gastroenterol. 2010 Mar;105(3):691-6. doi: 10.1038/ajg.2009.642. Epub 2009 Nov 10. Am J Gastroenterol. 2010. PMID: 19904244
Novel Variant in the USP9X Gene Is Associated with Congenital Heart Disease in a Male Patient: A Case Report and Literature Review.
Agazzi C, Magliozzi M, Iacoviello O, Palladino S, Delvecchio M, Masciopinto M, Galati A, Novelli A, Causio FA, Zampino G, Ruggiero C, Fischetto R. Agazzi C, et al. Among authors: delvecchio m. Mol Syndromol. 2023 Apr;14(2):158-163. doi: 10.1159/000527424. Epub 2022 Dec 23. Mol Syndromol. 2023. PMID: 37064340 Free PMC article.
169 results