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Page 1
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. Among authors: alberico f. Diabetes Metab. 2022 Sep;48(5):101353. doi: 10.1016/j.diabet.2022.101353. Epub 2022 Apr 26. Diabetes Metab. 2022. PMID: 35487478
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: alberico f. Pharmacogenomics J. 2018 May 22;18(3):431-435. doi: 10.1038/tpj.2017.32. Epub 2017 Jul 11. Pharmacogenomics J. 2018. PMID: 28696414
IRS1 G972R missense polymorphism is associated with failure to oral antidiabetes drugs in white patients with type 2 diabetes from Italy.
Prudente S, Morini E, Lucchesi D, Lamacchia O, Bailetti D, Mercuri L, Alberico F, Copetti M, Pucci L, Fariello S, Giusti L, Cignarelli M, Penno G, De Cosmo S, Trischitta V. Prudente S, et al. Among authors: alberico f. Diabetes. 2014 Sep;63(9):3135-40. doi: 10.2337/db13-1966. Epub 2014 Jun 19. Diabetes. 2014. PMID: 24947357 Free article.
Infrequent TRIB3 coding variants and coronary artery disease in type 2 diabetes.
Prudente S, Bailetti D, Mendonca C, Mannino GC, Fontana A, Andreozzi F, Hastings T, Mercuri L, Alberico F, Basile G, Copetti M, Sesti G, Doria A, Trischitta V. Prudente S, et al. Among authors: alberico f. Atherosclerosis. 2015 Sep;242(1):334-9. doi: 10.1016/j.atherosclerosis.2015.07.030. Epub 2015 Jul 17. Atherosclerosis. 2015. PMID: 26253791 Free PMC article.
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: alberico f. Nephrol Dial Transplant. 2017 Oct 1;32(10):1718-1722. doi: 10.1093/ndt/gfw262. Nephrol Dial Transplant. 2017. PMID: 27448670
Contribution of ONECUT1 variants to different forms of non-autoimmune diabetes mellitus in Italian patients.
Prudente S, Andreozzi F, Mercuri L, Alberico F, Di Giamberardino A, Mannino GC, Ludovico O, Piscitelli P, Di Paola R, Morano S, Penno G, Carella M, De Cosmo S, Trischitta V, Barbetti F. Prudente S, et al. Among authors: alberico f. Acta Diabetol. 2022 Aug;59(8):1113-1116. doi: 10.1007/s00592-022-01889-w. Epub 2022 Apr 28. Acta Diabetol. 2022. PMID: 35482136 No abstract available.
Joint effect of insulin signaling genes on insulin secretion and glucose homeostasis.
Prudente S, Morini E, Marselli L, Baratta R, Copetti M, Mendonca C, Andreozzi F, Chandalia M, Pellegrini F, Bailetti D, Alberico F, Shah H, Abate N, Sesti G, Frittitta L, Marchetti P, Doria A, Trischitta V. Prudente S, et al. Among authors: alberico f. J Clin Endocrinol Metab. 2013 Jun;98(6):E1143-7. doi: 10.1210/jc.2012-4282. Epub 2013 Apr 30. J Clin Endocrinol Metab. 2013. PMID: 23633196 Free PMC article.
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: alberico f. Acta Diabetol. 2019 May;56(5):515-523. doi: 10.1007/s00592-018-01283-5. Epub 2019 Jan 17. Acta Diabetol. 2019. PMID: 30656436
17 results