VALENTI, Vincenza
VALENTI, Vincenza
Biomedico di Medicina Interna e Specialistica (attivo dal 01/01/2013 al 31/12/2018)
Baseline metabolic disturbances and the twenty-five years risk of incident cancer in a Mediterranean population
2016-01-01 Noto, D.; Cefalu', A.; Barbagallo, C.; Ganci, A.; Cavera, G.; Fayer, F.; Palesano, O.; Spina, R.; Valenti, V.; Altieri, G.; Caldarella, R.; Giammanco, A.; Termini, R.; Burrascano, M.; Crupi, G.; Falletta, A.; Scafidi, V.; Sbordone, D.; La Seta, F.; Averna, M.
Familial hypobetalipoproteinemia due to apolipoprotein B R463W mutation causes intestinal fat accumulation and low postprandial lipemia.
2009-01-01 Noto, D; Cefalù, AB; Cannizzaro, A; Minà, M; Fayer, F; Valenti, V; Barbagallo, CM; Tuttolomondo, A; Pinto, A; Sciumè, C; Licata, G; Averna, M
Genetic epidemiology of autosomal recessive hypercholesterolemia in Sicily: Identification by next-generation sequencing of a new kindred
2018-01-01 Spina, R.; Noto, D.; Barbagallo, C.; Monastero, R.; Ingrassia, V.; Valenti, V.; Baschi, R.; Pipitone, A.; Giammanco, A.; La Spada, M.; Misiano, G.; Scrimali, C.; Cefalu', A.; Averna, M.
Homozygous familial hypobetalipoproteinemia: Two novel mutations in the splicing sites of apolipoprotein B gene and review of the literature
2015-01-01 Cefalù, A.; Norata, G.; Ghiglioni, D.; Noto, D.; Uboldi, P.; Garlaschelli, K.; Baragetti, A.; Spina, R.; Valenti, V.; Pederiva, C.; Riva, E.; Terracciano, L.; Zoja, A.; Grigore, L.; Averna, M.; Catapano, A.
Identification of a novel LMF1 nonsense mutation responsible for severe hypertriglyceridemia by targeted next-generation sequencing
2017-01-01 Cefalu', A; Spina, R; Noto, D; Ingrassia, V.; Valenti, V; Giammanco, A; Fayer, F; Misiano, G; Cocorullo, G; Scrimali, C; Palesano, O; Altieri, G; Ganci, A; Barbagallo, C; Averna, M
IL GENE PCSK9: UN NUOVO GENE IMPLICATO NEL CONTROLLO DELLA COLESTEROLEMIA
2007-01-01 CEFALU' AB; AMATO S; FERTITTA E; FAYER F; VALENTI V; GUELI MC; DI BLASI U; PAGANO M; NARDI I; CUSUMANO G; GULOTTA P; RAFFA A; DOVERI T; AVERNA MR
LE IPERCOLESTEROLEMIE PRIMITIVE
2007-01-01 NOTO N; AMATO S; FERTITTA E; FAYER F; VALENTI V; GUELI MC; DI BLASI U; PAGANO M; NARDI I; CUSUMANO G; GULOTTA P; RAFFA A; DOVERI T; AVERNA MR
Le LDL generate in fase post-prandiale dopo carico grasso presentano maggiore densita’, minore size e maggiore affinita’ per il recettore
2004-01-01 Noto, D; Rizzo, M; Pace, A; Fayer, F; Mina’, M; Lo Verde, A; Onorato, K; Valenti, V; Barraco, G; Cefalu’, AB; Barbagallo, CM; Notarbartolo, A; Averna, MR
Myristic acid is associated to low plasma HDL cholesterol levels in a Mediterranean population and increases HDL catabolism by enhancing HDL particles trapping to cell surface proteoglycans in a liver hepatoma cell model
2016-01-01 Noto, D.; Fayer, F.; Cefalù, A.; Altieri, I.; Palesano, O.; Spina, R.; Valenti, V.; Pitrone, M.; Pizzolanti, G.; Barbagallo, C.; Giordano, C.; Averna, M.
A Novel APOB Mutation Identified by Exome Sequencing Cosegregates With Steatosis, Liver Cancer, and Hypocholesterolemia.
2013-01-01 Cefalù, AB; Pirruccello, JP; Noto, D; Gabriel, S; Valenti, V; Gupta, N; Spina, R; Tarugi, P; Kathiresan, S; Averna, M
Novel CREB3L3 Nonsense Mutation in a Family With Dominant Hypertriglyceridemia
2015-01-01 Cefalù, A.; Spina, R.; Noto, D.; Valenti, V.; Ingrassia, V.; Giammanco, A.; Panno, M.; Ganci, A.; Barbagallo, C.; Averna, M.
A novel loss of function mutation of PCSK9 gene in white subjects with low-plasma low-density lipoprotein cholesterol.
2007-01-01 FASANO, T; CEFALU, AB; DI LEO, E; NOTO, D; POLLACCIA, D; BOCCHI, L; VALENTI, V; BONARDI, R; GUARDAMAGNA, O; AVERNA, M; TARUGI, P
A novel mutation of the extracellular matrix protein 1 gene (ECM1) in a patient with lipoid proteinosis (Urbach-Wiethe disease) from Sicily
2005-01-01 LUPO, I; CEFALU', AB; BONGIORNO, MR; DANIELE, O; VALENTI, V; NOTO, D; CAMARDA, R; SAVETTIERI, G; ARICO', M; AVERNA M
Obesity and the metabolic syndrome in a student cohort from Southern Italy
2009-01-01 Noto, D; Niglio, T; Cefalù, AB; Martino, E; Fayer, F; Mina, M; Valenti, V; Notarbartolo, A; Averna, M; Martino, F
The PCSK9 gene: a new gene controlling cholesterolemia
2007-01-01 Cefalu, AB; Amato, S; Fertitta, E; Fayer, F; Valenti, V; Gueli, MC; Di Blasi, U; Pagano, M; Nardi, IB; Cusumano, G; Gulotta, P; Raffa, A; Doveri, T; Averna, M
Prevalence of ANGPTL3 and APOB gene mutations in subjects with combined hypolipidemia
2012-01-01 Noto, D; Cefalù, A; Valenti, V; Fayer, F; Pinotti, E; Ditta, M; Spina, R; Vigna, G; Yue, P; Kathiresan, S; Tarugi, P; Averna, M
Six novel mutations of the LDL receptor gene in FH kindred of Sicilian and Paraguayan descent
2006-01-01 CEFALU, AB; BARRACO, G; NOTO, D; VALENTI, V; BARBAGALLO, CM; ELISIR, GD; CUNIBERTI, LA; WERBA, JP; LIBRA, M; COSTA, S; GIANGUZZA, F; NOTARBARTOLO, A; TRAVALI, S; AVERNA, M