AVERNA, Maurizio
AVERNA, Maurizio
Promozione della Salute, Materno-Infantile, di Medicina Interna e Specialistica di Eccellenza “G. D’Alessandro”
A genetic variant of the atrial natriuretic peptide gene is associated with cardiometabolic protection in the general community
2011-01-01 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
A metallothionein family member interacts with the intracellular domain of the low density lipoprotein (ldl) receptor.
2007-01-01 COSTA S; NICOSIA A; RAGUSA MA; POLLACCIA D; VALENTI V; CEFALÙ AB; AVERNA MR; AND GIANGUZZA F
A new apolipoprotein B truncation (apo B-43.7) in familial hypobetalipoproteinemia: Genetic and metabolic studies
1996-01-01 Srivastava N.; Noto D.; Averna M.; Pulai J.; Srivastava R.A.K.; Cole T.G.; Latour M.A.; Patterson B.W.; Schonfeld G.
A NOVEL APOB MUTATION IDENTIFIED BY EXOME SEQUENCING COSEGREGATES WITH STEATOSIS, LIVER CANCER AND HYPOCHOLESTEROLEMIA
2013-01-01 Spina, R.; Cefalu', A.B.; Pirruccello, J.; Altieri, G.I.; Noto, D.; Gabriel, S.; Valenti, V.; Gupta, N.; Fayer, F.; Palesano, O.; Tarugi, P.; Kathiresan, S.; 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
A novel component of the metabolic syndrome : The oxidative stress
2010-01-01 Hopps, E; Noto, D; Caimi, G; Averna, M
A NOVEL COMPOUND HETEROZYGOUS MUTATION OF THE LIPOPROTEIN LIPASE GENE IN A NEWBORN WITH CHYLOMICRONEMIA
2005-01-01 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
A Novel Liquid Chromatography/Mass Spectrometry Method for Analysis of Plasma Sterol Concentrations
2006-01-01 Nagy, K.; Jakab, A.; Pollereisz, F.; Ceraulo, L.; Bongiorno, D.; Averna, M.; Noto, D.; Vekey, K.
A NOVEL LOSS OF FUCTION MUTATION OF PCSK9 GENE IN CAUCASIANS WITH LOW PLASMA LDL-CHOLESTEROL
2007-01-01 FASANO T; CEFALU' AB; DI LEO E; NOTO D; POLLACCIA D; BOCCHI L; VALENTI V; GUARDAMAGNA O; AVERNA M; TARUGI P
A NOVEL LOSS OF FUNCTION MUTATION OF PCSK9 GENE
2006-01-01 FASANO T; BOCCHI L; DI LEO E; CEFALU' AB; NOTO D; VALENTI V; GUARDAMAGNA O; CALANDRA S; AVERNA MR; TARUGI P
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 in the Lipase Maturaction Factor 1 (LMF-1)gene responsible for severe hypertriglyceridemia
2008-01-01 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
A Novel Mutation of the DHCR7 Gene in a Sicilian Compound Heterozygote with Smith-Lemli-Opitz Syndrome
2005-01-01 ROMANO F; FIORE B; PEZZINO FM; LONGOMBARDO MT; CEFALU' AB; NOTO D; PUGLISI A; BROGNA A; MATTINA T; AVERNA M; TRAVALI S
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
A novel nonsense mutation in the cept gene in italian Hyperalphalipoproteinemic subjects
2004-01-01 Buglino, C.; Martini, S.; Cefalu', A.; Noto, D.; Cortella, I.; Mina', M.; Valenti, V.; Barbagallo, C.; Fayer, F.; Notarbartolo, A.; Averna, M.
A NOVEL NONSENSE MUTATION IN THE CETP GENE IN ITALIAN HYPERALPHALIPOPROTEINEMIC SUBJECTS
2006-01-01 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.
A novel putative interactor for the low density lipoprotein receptor cytoplasmic domain
2010-01-01 Costa, S; Nicosia, A; Ragusa, MA; Cefalù, AB; Pollaccia, D; Noto, D; Averna, M; Gianguzza, F
A polymorphism in the cyclooxygenase 2 gene as an inherited protective factor against myocardial infarction and stroke
2004-01-01 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
A subgroup analysis of the ODYSSEY APPRISE study: Safety and efficacy of alirocumab in the Italian cohort
2022-08-09 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
A Targeted ApoB38.9 Mutation in Mice Is Associated with Reduced Hepatic Cholesterol Synthesis and Enhanced Lipid Peroxidation.
2006-01-01 LIN X; CHEN Z; YUE P; AVERNA M; OSTLUND JR RE; WATSON MA; SCHONFELD G
| 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-1996 | A new apolipoprotein B truncation (apo B-43.7) in familial hypobetalipoproteinemia: Genetic and metabolic studies | Srivastava N.Noto D.Averna M. + | 01 - Contributo in rivista::1.01 Articolo in rivista | Srivastava N.; Noto D.; Averna M.; Pulai J.; Srivastava R.A.K.; Cole T.G.; Latour M.A.; Patterson B.W.; Schonfeld G. | |
| 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 + | 01 - Contributo in rivista::1.05 Abstract in atti di convegno pubblicato in rivista | Spina, R.; Cefalu', A.B.; Pirruccello, J.; Altieri, G.I.; 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 |