AVERNA, Maurizio

AVERNA, Maurizio  

Promozione della Salute, Materno-Infantile, di Medicina Interna e Specialistica di Eccellenza “G. D’Alessandro”  

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Data di pubblicazione Titolo Autori Tipologia Autore(i) File
1-gen-2011 A genetic variant of the atrial natriuretic peptide gene is associated with cardiometabolic protection in the general community AVERNA, Maurizio + 01 - Contributo in rivista::1.01 Articolo in rivista Cannone V; Boerrigter G; Cataliotti A; Costello-Boerrigter LC; Olson TM; McKie PM; Heublein DM; Lahr BD; Bailey KR; Averna M; Redfield MM; Rodeheffer RJ; Burnett JC Jr
1-gen-2007 A metallothionein family member interacts with the intracellular domain of the low density lipoprotein (ldl) receptor. COSTA, SalvatoreNICOSIA, AldoRAGUSA, Maria AntoniettaPOLLACCIA, DanielaVALENTI, VincenzaCEFALU', Angelo BaldassareAVERNA, MaurizioGIANGUZZA, Fabrizio 10 - Proceedings::Proceedings COSTA S; NICOSIA A; RAGUSA MA; POLLACCIA D; VALENTI V; CEFALÙ AB; AVERNA MR; AND GIANGUZZA F
1-gen-2013 A NOVEL APOB MUTATION IDENTIFIED BY EXOME SEQUENCING COSEGREGATES WITH STEATOSIS, LIVER CANCER AND HYPOCHOLESTEROLEMIA SPINA, RossellaCEFALU', Angelo BaldassareALTIERI, Grazia IdaNoto, DVALENTI, VincenzaFAYER, FrancescaPALESANO, OrnellaAVERNA, Maurizio + 10 - Proceedings::Proceedings Spina, R; Cefalù AB; Pirruccello, JP; Altieri, GI; Noto, D; Gabriel, S; Valenti, V; Gupta, N; Fayer, F; Palesano, O; Tarugi, P; Kathiresan, S; Averna, M
1-gen-2013 A Novel APOB Mutation Identified by Exome Sequencing Cosegregates With Steatosis, Liver Cancer, and Hypocholesterolemia. CEFALU', Angelo BaldassareNOTO, DavideVALENTI, VincenzaSPINA, RossellaAVERNA, Maurizio + 01 - Contributo in rivista::1.01 Articolo in rivista Cefalù, AB; Pirruccello, JP; Noto, D; Gabriel, S; Valenti, V; Gupta, N; Spina, R; Tarugi, P; Kathiresan, S; Averna, M
1-gen-2010 A novel component of the metabolic syndrome : The oxidative stress HOPPS, EugeniaNOTO, DavideCAIMI, GregorioAVERNA, Maurizio 01 - Contributo in rivista::1.01 Articolo in rivista Hopps, E; Noto, D; Caimi, G; Averna, M
1-gen-2005 A NOVEL COMPOUND HETEROZYGOUS MUTATION OF THE LIPOPROTEIN LIPASE GENE IN A NEWBORN WITH CHYLOMICRONEMIA VALENTI, VincenzaCEFALU', Angelo BaldassareBARRACO, GiacomaFAYER, FrancescaVIVONA, NicolettaMINA', MariangelaONORATO, KarolyPOLLACCIA, DanielaBUGLINO, Carmela MariaBARBAGALLO, Carlo MariaNOTARBARTOLO, AlbertoAVERNA, Maurizio + 10 - Proceedings::Proceedings VALENTI, V; CEFALU, AB; NOTO, D; BARRACO, G; FAYER, F; VIVONA, N; MINA, M; ONORATO, K; POLLACCIA, D; BUGLINO, C; BARBAGALLO, CM; NOTARBARTOLO, A; AVERNA, MR
1-gen-2006 A Novel Liquid Chromatography/Mass Spectrometry Method for Analysis of Plasma Sterol Concentrations CERAULO, LeopoldoBONGIORNO, DavidAVERNA, Maurizio + 10 - Proceedings::Proceedings Nagy, K.; Jakab, A.; Pollereisz, F.; Ceraulo, L.; Bongiorno, D.; Averna, M.; Noto, D.; Vekey, K.
1-gen-2007 A NOVEL LOSS OF FUCTION MUTATION OF PCSK9 GENE IN CAUCASIANS WITH LOW PLASMA LDL-CHOLESTEROL CEFALU', Angelo BaldassareNOTO DPOLLACCIA, DanielaVALENTI, VincenzaAVERNA, Maurizio + 10 - Proceedings::Proceedings FASANO T; CEFALU' AB; DI LEO E; NOTO D; POLLACCIA D; BOCCHI L; VALENTI V; GUARDAMAGNA O; AVERNA M; TARUGI P
1-gen-2006 A NOVEL LOSS OF FUNCTION MUTATION OF PCSK9 GENE CEFALU', Angelo BaldassareVALENTI, VincenzaAVERNA, Maurizio + 10 - Proceedings::Proceedings FASANO T; BOCCHI L; DI LEO E; CEFALU' AB; NOTO D; VALENTI V; GUARDAMAGNA O; CALANDRA S; AVERNA MR; TARUGI P
1-gen-2007 A novel loss of function mutation of PCSK9 gene in white subjects with low-plasma low-density lipoprotein cholesterol. CEFALU', Angelo BaldassareNOTO, DavidePOLLACCIA, DanielaVALENTI, VincenzaAVERNA, Maurizio + 01 - Contributo in rivista::1.01 Articolo in rivista FASANO, T; CEFALU, AB; DI LEO, E; NOTO, D; POLLACCIA, D; BOCCHI, L; VALENTI, V; BONARDI, R; GUARDAMAGNA, O; AVERNA, M; TARUGI, P
1-gen-2008 A novel mutation in the Lipase Maturaction Factor 1 (LMF-1)gene responsible for severe hypertriglyceridemia SPINA, RossellaVIVONA, NicolettaNoto, DCEFALU', Angelo BaldassareNOTARBARTOLO, AlbertoAVERNA, Maurizio + 10 - Proceedings::Proceedings Spina, R; Arpi, ML; Vivona, N; Ditta, M; Fayer, F; Minà, M; Valenti, V; Pollaccia, D; Noto, D; Cefalù, AB; Notarbartolo, A; Vigneti, R; Averna, MR
1-gen-2005 A Novel Mutation of the DHCR7 Gene in a Sicilian Compound Heterozygote with Smith-Lemli-Opitz Syndrome CEFALU', Angelo BaldassareNOTO, DavideAVERNA, Maurizio + 01 - Contributo in rivista::1.01 Articolo in rivista ROMANO F; FIORE B; PEZZINO FM; LONGOMBARDO MT; CEFALU' AB; NOTO D; PUGLISI A; BROGNA A; MATTINA T; AVERNA M; TRAVALI S
1-gen-2005 A novel mutation of the extracellular matrix protein 1 gene (ECM1) in a patient with lipoid proteinosis (Urbach-Wiethe disease) from Sicily LUPO, InnocenzoCEFALU', Angelo BaldassareBONGIORNO, Maria RitaDANIELE, OrnellaVALENTI, VincenzaCAMARDA, RosolinoSAVETTIERI, GiovanniARICO', MarioAVERNA, Maurizio + 01 - Contributo in rivista::1.01 Articolo in rivista LUPO, I; CEFALU', AB; BONGIORNO, MR; DANIELE, O; VALENTI, V; NOTO, D; CAMARDA, R; SAVETTIERI, G; ARICO', M; AVERNA M
1-gen-2004 A novel nonsense mutation in the cept gene in italian Hyperalphalipoproteinemic subjects BUGLINO, Carmela MariaCEFALU', Angelo BaldassareMINA', MariangelaVALENTI, VincenzaBARBAGALLO, Carlo MariaFAYER, FrancescaNOTARBARTOLO, AlbertoAVERNA, Maurizio + 10 - Proceedings::Proceedings Buglino, C.; Martini, S.; Cefalu', A.; Noto, D.; Cortella, I.; Mina', M.; Valenti, V.; Barbagallo, C.; Fayer, F.; Notarbartolo, A.; Averna, M.
1-gen-2006 A NOVEL NONSENSE MUTATION IN THE CETP GENE IN ITALIAN HYPERALPHALIPOPROTEINEMIC SUBJECTS CEFALU', Angelo BaldassareNOTO, DavideVALENTI, VincenzaFAYER, FrancescaGUELI, Maria ConcettaBARBAGALLO, Carlo MariaAVERNA, MaurizioMINA', MariangelaBUGLINO, Carmela Maria + 10 - Proceedings::Proceedings CEFALU'; AB; MARTINI S; NOTO D; CORTELLA I; VALENTI V; FAYER F; GUELI MC; BARBAGALLO CM; NOTARBARTOLO A; AVERNA M; Mina', M.; Buglino, C.M.
1-gen-2010 A novel putative interactor for the low density lipoprotein receptor cytoplasmic domain COSTA, SalvatoreNICOSIA, AldoRAGUSA, Maria AntoniettaCEFALU', Angelo BaldassarePOLLACCIA, DanielaNoto, DAVERNA, MaurizioGIANGUZZA, Fabrizio 01 - Contributo in rivista::1.01 Articolo in rivista Costa, S; Nicosia, A; Ragusa, MA; Cefalù, AB; Pollaccia, D; Noto, D; Averna, M; Gianguzza, F
1-gen-2004 A polymorphism in the cyclooxygenase 2 gene as an inherited protective factor against myocardial infarction and stroke AVERNA, Maurizio + 01 - Contributo in rivista::1.01 Articolo in rivista CIPOLLONE F; TONIATO E; MARTINOTTI S; FAZIA M; IEZZI A; CUCCURULLO C; PINI B; URSI S; VITULLO G; AVERNA M; ARCA M; MONTALI A; CAMPAGNA F; UCCHINO S; SPIGONARDO F; TADDEI S; VIRDIS A; CIABATTONI G; NOTARBARTOLO A; CUCCURULLO F; MEZZETTI A; IDENTIFICATION OF NEW ELEMENTS OF PLAQUE STABILITY INES STUDY GROUP
9-ago-2022 A subgroup analysis of the ODYSSEY APPRISE study: Safety and efficacy of alirocumab in the Italian cohort Cefalu', Angelo BAverna, Maurizio + 01 - Contributo in rivista::1.01 Articolo in rivista Cefalu', Angelo B; Garbelotto, Raffaella; Mombelli, Giuliana; Pirro, Matteo; Rubba, Paolo; Arca, Marcello; Borghi, Claudio; Bonomo, Katia; Gonnelli, Stefano; Massaroni, Katia; Tirone, Giampaolo; Averna, Maurizio
1-gen-2006 A Targeted ApoB38.9 Mutation in Mice Is Associated with Reduced Hepatic Cholesterol Synthesis and Enhanced Lipid Peroxidation. AVERNA, Maurizio + 01 - Contributo in rivista::1.01 Articolo in rivista LIN X; CHEN Z; YUE P; AVERNA M; OSTLUND JR RE; WATSON MA; SCHONFELD G
1-gen-2006 Accumulation of apoE-enriched triglyceride-rich lipoproteins in patients with coronary artery disease BARBAGALLO, Carlo MariaRIZZO, ManfrediNoto, DCEFALU', Angelo BaldassareAVERNA, MaurizioGIORDANO, CarlaNOTARBARTOLO, Alberto + 01 - Contributo in rivista::1.01 Articolo in rivista Barbagallo, CM; Rizzo, M; Noto, D; Frasheri, A; Pernice, V; Rubino, A; Pieri, D; Pinto, V; Cefalu', AB; Giordano, C ;Notarbartolo, A; Averna, M