FAYER, Francesca
FAYER, Francesca
Biomedico di Medicina Interna e Specialistica (attivo dal 01/01/2013 al 31/12/2018)
A NOVEL APOB MUTATION IDENTIFIED BY EXOME SEQUENCING COSEGREGATES WITH STEATOSIS, LIVER CANCER AND HYPOCHOLESTEROLEMIA
2013-01-01 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
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 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.
Apolipoprotein AI and HDL are reduced in stable cirrhotic patients with adrenal insufficiency: A possible role in glucocorticoid deficiency
2015-01-01 Spadaro, L.; Noto, D.; Privitera, G.; Tomaselli, T.; Fede, G.; Scicali, R.; Piro, S.; Fayer, F.; Altieri, I.; Averna, M.; Purrello, F.
ASSOCIATION OF THE PARAOXONASE-1 Q192R POLYMORPHISM WITH CORONARY ARTERY DISEASE IN AMI PATIENTS, NON AMI CAD AND HEALTHY CONTROLS.
2004-01-01 MINA M; ONORATO K; FAYER F; CALDARELLA R; NOVO G; VALENTI V; BARRACO G; DAVI V; CEFALU' AB; BUGLINO C; NOTO D; NOTARBARTOLO, A; AVERNA, M
ASSOCIAZIONE DEL POLIMORFISMO Q192R DEL GENE DELLA PARAOXONASI I (PON1) CON LA MALATTIA CORONARICA IN UN CAMPIONE DI PZ CON INFARTO MIOCARDICO, MALATTIA CORONARICA NON INFARTUALE E SOGGETTI NORMALI.
2004-01-01 MINA M; NOTO D; FAYER F; ONORATO K; VALENTI V; CALDARELLA R; SEGRETO S; SCIMECA A; ONORATO F; CEFALU' AB; BARBAGALLO CM; NOTARBARTOLO A; AVERNA MR
Autoimmunity Features in Patients With Non-Celiac Wheat Sensitivity
2021-01-01 Mansueto, Pasquale; Soresi, Maurizio; Candore, Giuseppina; Garlisi, Chiara; Fayer, Francesca; Gambino, Caterina Maria; La Blasca, Francesco; Seidita, Aurelio; DʼAlcamo, Alberto; Lo Sasso, Bruna; Florena, Ada Maria; Geraci, Girolamo; Caio, Giacomo; Volta, Umberto; De Giorgio, Roberto; Ciaccio, Marcello; Carroccio, Antonio
Body Mass Index and Associated Clinical Variables in Patients with Non-Celiac Wheat Sensitivity
2019-05-29 Mansueto P., Soresi M., La Blasca F., Fayer F., D'Alcamo A., Carroccio A.
CEREBROTENDINOUS XANTHOMATOSIS: A SICILIAN FAMILY HARBOURING THE R362C MUTATION IN THE STEROL 27-HYDROXYLASE GENE
2006-01-01 VIVONA, N; BARRACO, G; VALENTI, V; CEFALU', AB; NOTO, D; POLLACCIA, D; FAYER, F; MINA', M; BARBAGALLO, CM; NOTARBARTOLO, A; BAGGIO, G; AVERNA, M
Clinical symptoms in celiac patients on a gluten-free diet.
2008-01-01 CARROCCIO A; AMBROSIANO G; DI PRIMA L; PIRRONE G; IACONO G; FLORENA AM; PORCASI R; NOTO D; FAYER F; SORESI M; GERACI G; SCIUMÈ C; DI FEDE G
COMPOUND HETEROZYGOUS FH AND FDB: IDENTIFICATION OF A SICILIAN FAMILY HARBOURING THE FDB3531 MUTATION AND THE Y398X MUTATION OF THE LDL RECEPTOR GENE.
2006-01-01 VIVONA, N; CEFALU', AB; POLLACCIA, D; VALENTI, V; BARRACO, G; NOTO, D; ONORATO, K; FAYER, F; MINA', M; BARBAGALLO, CM; NOTARBARTOLO, A; TRAVALI, S; AVERNA, MR
Contact dermatitis due to nickel allergy in patients suffering from non-celiac wheat sensitivity
2017-01-01 D'Alcamo, A.; Mansueto, P.; Soresi, M.; Iacobucci, R.; La Blasca, F.; Geraci, G.; Cavataio, F.; Fayer, F.; Arini, A.; DI STEFANO, L.; Iacono, G.; Bosco, L.; Carroccio, A.
DeepSRE: Identification of sterol responsive elements and nuclear transcription factors Y proximity in human DNA by Convolutional Neural Network analysis
2021-01-01 Noto D.; Giammanco A.; Spina R.; Fayer F.; Cefalu A.B.; Averna M.
DETECTION OF NEW GENES RESPONSIBLE OF FAMILIAL RECESSIVE HYPERCHOLESTEROLEMIA: PRELIMINARY DATA FROM AN EXOME SEQUENCING APPROACH
2014-01-01 Spina, R.; Cefalù, A.; Valenti, V.; Noto, D.; Ingrassia, V.; Scrimali, C.; Spada, M.; Misiano, G.; Altieri, G.; Fayer, F.; Barbagallo, C.; Palesano, O.; Licata, V.; Averna, M.
Duodenal and Rectal Mucosa Inflammation in Patients With Non-celiac Wheat Sensitivity
2019-01-01 Carroccio, Antonio; Giannone, Giulio; Mansueto, Pasquale; Soresi, Maurizio; La Blasca, Francesco; Fayer, Francesca; Iacobucci, Rosario; Porcasi, Rossana; Catalano, Tiziana; Geraci, Girolamo; Arini, Andrea; D'Alcamo, Alberto; Villanacci, Vincenzo; Florena, Ada M.
Erratum: FragClust and TestClust, two informatics tools for chemical structure hierarchical clustering analysis applied to lipidomics. The example of Alzheimer's disease (Analytical and Bioanalytical Chemistry DOI: 10.1007/s00216-015-9229-6)
2016-01-01 Francesca Di Gaudio; Sergio Indelicato; Roberto Monastero; Grazia Ida Altieri; Francesca Fayer; Ornella Palesano; Manuela Fontana; Angelo B. Cefalu; Massimiliano Greco; David Bongiorno; Serena Indelicato; Angela Aronica; Davide Noto; Maurizio Averna;
Evaluation of tolerability of “ancient” grains in patients with NCGS.
2021-01-01 Pistone M., Mansueto P., La Blasca F., Fayer F., Seidita A., Carroccio A.
FAMILIAL HYPOBETALIPOPROTEINEMIA DUE TO APOLIPOPROTEIN B GENE MUTATIONS CAUSES INTESTINAL FAT ACCUMULATION AND LIPID MALABSORPTION.
2007-01-01 Noto, D.; Cefalu', A.; Mina', M.; Carroccio, A.; Barbagallo, C.; Montalcini, T.; DI PRIMA, L.; Fayer, F.; Pujia, A.; Notarbartolo, A.; 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