MICCOLI, SARA

MICCOLI, SARA  

Risultati 1 - 11 di 11 (tempo di esecuzione: 0.014 secondi).
Titolo Autore(i) Anno Periodico Editore Tipo File
BRCA1 p.His1673del is a pathogenic mutation associated with a predominant ovarian cancer phenotype Zuntini, Roberta; Cortesi, Laura; Calistri, Daniele; Pippucci, Tommaso; Martelli, Pier Luigi; Casadio, Rita; Capizzi, Elisa; Santini, Donatella; Miccoli, Sara; Medici, Veronica; Danesi, Rita; Marchi, Isabella; Zampiga, Valentina; Fiorentino, Michelangelo; Ferrari, Simona; Turchetti, Daniela 2017-01-01 ONCOTARGET - 1.01 Articolo in rivista -
CDKN2A and BAP1 germline mutations predispose to melanoma and mesothelioma Betti, M.; Aspesi, A.; Biasi, A.; Casalone, E.; Ferrante, D.; Ogliara, P.; Gironi, L.C.; Giorgione, R.; Farinelli, P.; Grosso, F.; Libener, R.; Rosato, S.; Turchetti, D.; Maffè, A.; Casadio, C.; Ascoli, V.; Dianzani, C.; Colombo, E.; Piccolini, E.; Pavesi, M.; Miccoli, S.; Mirabelli, D.; Bracco, C.; Righi, L.; Boldorini, R.; Papotti, M.; Matullo, G.; Magnani, C.; Pasini, B.; Dianzani, I. 2016-01-01 CANCER LETTERS - 1.01 Articolo in rivista Betti_2016.pdf
Chromoendoscopy is not superior to white light endoscopy in improving adenoma detection in Lynch Syndrome cohort undergoing surveillance with high-resolution colonoscopy: a real-world evidence study Montale, Amedeo; Buttitta, Francesco; Pierantoni, Chiara; Ferrari, Clarissa; Cameletti, Michela; Colussi, Dora; Miccoli, Sara; Bazzoli, Franco; Turchetti, Daniela; Ricciardiello, Luigi 2021-01-01 DIGESTIVE DISEASES - 1.01 Articolo in rivista -
Clinical histopathological features and CDKN2A/CDK4/MITF mutational status of patients with multiple primary melanomas from Bologna: Italy is a fascinating but complex mosaic Dika E.; Patrizi A.; Rossi C.; Turchetti D.; Miccoli S.; Ferracin M.; Veronesi G.; Scarfi F.; Lambertini M. 2021-01-01 ITALIAN JOURNAL OF DERMATOLOGY AND VENEREOLOGY - 1.01 Articolo in rivista -
Colorectal polyposis as a clue to the diagnosis of Cowden syndrome: Report of two cases and literature review Innella G.; Miccoli S.; Colussi D.; Pradella L.M.; Amato L.B.; Zuntini R.; Salfi N.C.M.; Collina G.; Ferrara F.; Ricciardiello L.; Turchetti D. 2021-01-01 PATHOLOGY RESEARCH AND PRACTICE - 1.01 Articolo in rivista -
Dealing With BRCA1/2 unclassified variants in a cancer genetics clinic: Does cosegregation analysis help? Zuntini, Roberta; Ferrari, Simona; Bonora, Elena; Buscherini, Francesco; Bertonazzi, Benedetta; Grippa, Mina; Godino, Lea; Miccoli, Sara; Turchetti, Daniela* 2018-01-01 FRONTIERS IN GENETICS - 1.01 Articolo in rivista fgene-09-00378.pdf
miR-155 Is Downregulated in Familial Adenomatous Polyposis and Modulates WNT Signaling by Targeting AXIN1 and TCF4 Prossomariti, Anna; Piazzi, Giulia; D'Angelo, Leonarda; Miccoli, Sara; Turchetti, Daniela; Alquati, Chiara; Montagna, Claudio; Bazzoli, Franco; Ricciardiello, Luigi 2018-01-01 MOLECULAR CANCER RESEARCH - 1.01 Articolo in rivista -
Preferences of Italian patients for return of secondary findings from clinical genome/exome sequencing Godino L.; Varesco L.; Bruno W.; Bruzzone C.; Battistuzzi L.; Franiuk M.; Miccoli S.; Bertonazzi B.; Graziano C.; Seri M.; Turchetti D. 2021-01-01 JOURNAL OF GENETIC COUNSELING - 1.01 Articolo in rivista -
PTEN Hamartoma Tumor Syndrome: Skin Manifestations and Insights Into Their Molecular Pathogenesis Innella G.; Bonora E.; Neri I.; Virdi A.; Guglielmo A.; Pradella L.M.; Ceccarelli C.; Amato L.B.; Lanzoni A.; Miccoli S.; Gasparre G.; Zuntini R.; Turchetti D. 2021-01-01 FRONTIERS IN MEDICINE - 1.01 Articolo in rivista -
Somatic APC mosaicism and oligogenic inheritance in genetically unsolved colorectal adenomatous polyposis patients Ciavarella, Michele; Miccoli, Sara; Prossomariti, Anna; Pippucci, Tommaso; Bonora, Elena; Buscherini, Francesco; Palombo, Flavia; Zuntini, Roberta; Balbi, Tiziana; Ceccarelli, Claudio; Bazzoli, Franco; Ricciardiello, Luigi; Turchetti, Daniela; Piazzi, Giulia 2018-01-01 EUROPEAN JOURNAL OF HUMAN GENETICS - 1.01 Articolo in rivista s41431-017-0086-y.pdf
Type and frequency of MUTYH variants in Italian patients with suspected MAP: A retrospective multicenter study Ricci, Maria Teresa; Miccoli, Sara; Turchetti, Daniela; Bondavalli, Davide; Viel, Alessandra; Quaia, Michele; Giacomini, Elisa; Gismondi, Viviana; Sanchez-Mete, Lupe; Stigliano, Vittoria; Martayan, Aline; Mazzei, Filomena; Bignami, Margherita; Bonelli, Luigina; Varesco, Liliana 2017-01-01 JOURNAL OF HUMAN GENETICS - 1.01 Articolo in rivista -