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Caring and living with Prader-Willi syndrome in Italy: integrating children, adults and parents' experiences through a multicentre narrative medicine research.
Ragusa L, Crinò A, Grugni G, Reale L, Fiorencis A, Licenziati MR, Faienza MF, Wasniewska M, Delvecchio M, Franzese A, Rutigliano I, Fusilli P, Corica D, Campana G, Greco D, Chiarito M, Sacco M, Toscano S, Marini MG. Ragusa L, et al. Among authors: faienza mf. BMJ Open. 2020 Aug 6;10(8):e036502. doi: 10.1136/bmjopen-2019-036502. BMJ Open. 2020. PMID: 32764084 Free PMC article.
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. Among authors: faienza mf. Diabetes Care. 2014 Dec;37(12):e258-60. doi: 10.2337/dc14-1788. Diabetes Care. 2014. PMID: 25414397 No abstract available.
Levothyroxine requirement in congenital hypothyroidism: a 12-year longitudinal study.
Delvecchio M, Salerno M, Vigone MC, Wasniewska M, Popolo PP, Lapolla R, Mussa A, Tronconi GM, D'Acunzo I, Di Mase R, Falcone RM, Corrias A, De Luca F, Weber G, Cavallo L, Faienza MF. Delvecchio M, et al. Among authors: faienza mf. Endocrine. 2015 Dec;50(3):674-80. doi: 10.1007/s12020-015-0574-1. Epub 2015 Mar 12. Endocrine. 2015. PMID: 25762444
192 results