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Genetic characterization of suspected MODY patients in Tunisia by targeted next-generation sequencing.
Dallali H, Pezzilli S, Hechmi M, Sallem OK, Elouej S, Jmel H, Ben Halima Y, Chargui M, Gharbi M, Mercuri L, Alberico F, Mazza T, Bahlous A, Ben Ahmed M, Jamoussi H, Abid A, Trischitta V, Abdelhak S, Prudente S, Kefi R. Dallali H, et al. Among authors: pezzilli s. Acta Diabetol. 2019 May;56(5):515-523. doi: 10.1007/s00592-018-01283-5. Epub 2019 Jan 17. Acta Diabetol. 2019. PMID: 30656436
Pathogenic variants of MODY-genes in adult patients with early-onset type 2 diabetes.
Pezzilli S, Mazza T, Scarale MG, Tang Y, Andreozzi F, Baroni MG, Buzzetti R, Cavallo MG, Cossu E, D'Angelo P, De Cosmo S, Lamacchia O, Leonetti F, Morano S, Morviducci L, Penno G, Pozzilli P, Pugliese G, Sesti G, Doria A, Trischitta V, Prudente S. Pezzilli S, et al. Acta Diabetol. 2022 May;59(5):747-750. doi: 10.1007/s00592-021-01847-y. Epub 2022 Feb 3. Acta Diabetol. 2022. PMID: 35112188 No abstract available.
Contribution of rare variants in monogenic diabetes-genes to early-onset type 2 diabetes.
Pezzilli S, Tohidirad M, Biagini T, Scarale MG, Alberico F, Mercuri L, Mannino GC, Garofolo M, Filardi T, Tang Y, Giuffrida F, Mendonca C, Andreozzi F, Baroni MG, Buzzetti R, Cavallo MG, Cossu E, D'Angelo P, De Cosmo S, Lamacchia O, Leonetti F, Morano S, Morviducci L, Penno G, Pozzilli P, Pugliese G, Sesti G, Mazza T, Doria A, Trischitta V, Prudente S. Pezzilli S, et al. Diabetes Metab. 2022 Sep;48(5):101353. doi: 10.1016/j.diabet.2022.101353. Epub 2022 Apr 26. Diabetes Metab. 2022. PMID: 35487478
The rs12917707 polymorphism at the UMOD locus and glomerular filtration rate in individuals with type 2 diabetes: evidence of heterogeneity across two different European populations.
Prudente S, Di Paola R, Copetti M, Lucchesi D, Lamacchia O, Pezzilli S, Mercuri L, Alberico F, Giusti L, Garofolo M, Penno G, Cignarelli M, De Cosmo S, Trischitta V. Prudente S, et al. Among authors: pezzilli s. Nephrol Dial Transplant. 2017 Oct 1;32(10):1718-1722. doi: 10.1093/ndt/gfw262. Nephrol Dial Transplant. 2017. PMID: 27448670
Gain of Function of Malate Dehydrogenase 2 and Familial Hyperglycemia.
Jungtrakoon Thamtarana P, Marucci A, Pannone L, Bonnefond A, Pezzilli S, Biagini T, Buranasupkajorn P, Hastings T, Mendonca C, Marselli L, Di Paola R, Abubakar Z, Mercuri L, Alberico F, Flex E, Ceròn J, Porta-de-la-Riva M, Ludovico O, Carella M, Martinelli S, Marchetti P, Mazza T, Froguel P, Trischitta V, Doria A, Prudente S. Jungtrakoon Thamtarana P, et al. Among authors: pezzilli s. J Clin Endocrinol Metab. 2022 Feb 17;107(3):668-684. doi: 10.1210/clinem/dgab790. J Clin Endocrinol Metab. 2022. PMID: 34718610 Free PMC article.
A functional variant of the dimethylarginine dimethylaminohydrolase-2 gene is associated with myocardial infarction in type 2 diabetic patients.
Mannino GC, Pezzilli S, Averta C, Fuoco A, Spiga R, Mancuso E, Di Fatta C, Perticone F, Prudente S, Trischitta V, Andreozzi F, Sesti G. Mannino GC, et al. Among authors: pezzilli s. Cardiovasc Diabetol. 2019 Aug 13;18(1):102. doi: 10.1186/s12933-019-0906-1. Cardiovasc Diabetol. 2019. PMID: 31409409 Free PMC article.
Pharmacogenetics of oral antidiabetes drugs: evidence for diverse signals at the IRS1 locus.
Prudente S, Di Paola R, Pezzilli S, Garofolo M, Lamacchia O, Filardi T, Mannino GC, Mercuri L, Alberico F, Scarale MG, Sesti G, Morano S, Penno G, Cignarelli M, Copetti M, Trischitta V. Prudente S, et al. Among authors: pezzilli s. Pharmacogenomics J. 2018 May 22;18(3):431-435. doi: 10.1038/tpj.2017.32. Epub 2017 Jul 11. Pharmacogenomics J. 2018. PMID: 28696414
14 results