Lea Godino; Daniela Turchetti; Heather Skirton, Genetic counseling: A survey to explore knowledge and attitudes of Italian nurses and midwives, «JOURNAL OF ADVANCED NURSING», 2013, 15, pp. 15 - 21 [articolo]
Godino L.; Turchetti D.; Skirton H., Knowledge of genetics and the role of the nurse in genetic health care: a survey of Italian nurses, «JOURNAL OF ADVANCED NURSING», 2013, 69, pp. 1125 - 1135 [articolo]
Annamaria Pollio;Aldo Tomasi;Stefania Seidenari;Giovanni Pellacani;Monica Rodolfo;Simona Frigerio;Andrea Maurichi;Daniela Turchetti;Sara Bassoli;Cristel Ruini;Giovanni Ponti, Malignant and benign tumors associated with multiple primary melanomas: just the starting block for the involvement ofMITF, PTENandCDKN2Ain multiple cancerogenesis?, «PIGMENT CELL & MELANOMA RESEARCH», 2013, 26, pp. 755 - 757 [articolo]
L. Varesco;V. Viassolo;A. Viel;V. Gismondi;P. Radice;M. Montagna;E. Alducci;L. Della Puppa;C. Oliani;S. Tommasi;M.A. Caligo;C. Vivanet;M. Zuradelli;P. Mandich;M.G. Tibiletti;P. Cavalli;E. Lucci Cordisco;D. Turchetti;D. Boggiani;R. Bracci;P. Bruzzi;L. Bonelli, Performance of BOADICEA and BRCAPRO genetic models and of empirical criteria based on cancer family history for predicting BRCA mutation carrier probabilities: A retrospective study in a sample of Italian cancer genetics clinics, «THE BREAST», 2013, 22, pp. 1130 - 1135 [articolo]
Pradella L.M.; Lang M.; Kurelac I.; Mariani E.; Guerra F.; Zuntini R.; Tallini G.; MacKay A.; Reis-Filho J.S.; Seri M.; Turchetti D.; Gasparre G., Where Birt-Hogg-Dubé meets Cowden Syndrome: Mirrored genetic defects in two cases of syndromic oncocytic tumours, «EUROPEAN JOURNAL OF HUMAN GENETICS», 2013, 21, pp. 1169 - 1172 [articolo]
Simonazzi G; Miccoli S; Salfi N; Bonasoni MP; Bocciardi R; Ravazzolo R; Seri M; Curti A; Pilu G; Rizzo N; Turchetti D., A novel p63 mutation in a fetus with ultrasound detection of split hand/foot malformation., «PRENATAL DIAGNOSIS», 2012, 32, pp. 296 - 298 [articolo]
CORTESI L.; DE NICOLO A.; MEDICI V.; MARINO M.; TURCHETTI D.; PRADELLA L.M.; ROSSI G.; PARISINI E.; FEDERICO M., COLLECTIVE EVIDENCE SUPPORTS NEUTRALITY OF BRCA1 V1687I, A NOVEL SEQUENCE VARIANT IN THE CONSERVED THV MOTIF OF THE FIRST BRCT REPEAT, «BREAST CANCER RESEARCH AND TREATMENT», 2012, 134, pp. 435 - 441 [articolo]
Marco Seri; Claudio Graziano; Daniela Turchetti; Juri Monducci, Test genetici e consenso informato, «SALUTE E SOCIETÀ», 2012, 3, pp. 68 - 95 [articolo]
Morandi L.; de Biase D.; Visani M.; Monzoni A.; Tosi A.; Brulatti M.; Turchetti D.; Baccarini P.; Tallini G.; Pession A., T([20]) repeat in the 3'-untranslated region of the MT1X gene: a marker with high sensitivity and specificity to detect microsatellite instability in colorectal cancer, «INTERNATIONAL JOURNAL OF COLORECTAL DISEASE», 2012, 27, pp. 647 - 656 [articolo]
Sardanelli F; Podo F; Santoro F; Manoukian S; Bergonzi S; Trecate G; Vergnaghi D; Federico M; Cortesi L; Corcione S; Morassut S; Di Maggio C; Cilotti A; Martincich L; Calabrese M; Zuiani C; Preda L; Bonanni B; Carbonaro LA; Contegiacomo A; Panizza P; Di Cesare E; Savarese A; Crecco M; Turchetti D; Tonutti M; Belli P; Maschio A Del; for the High Breast Cancer Risk Italian 1 (HIBCRIT-1) Study, Multicenter surveillance of women at high genetic breast cancer risk using mammography, ultrasonography, and contrast-enhanced magnetic resonance imaging (the high breast cancer risk italian 1 study): final results., «INVESTIGATIVE RADIOLOGY», 2011, 46, pp. 94 - 105 [articolo]
D. Turchetti; E. Pompilii; E. Magrini; P. Bonasoni; M. C. Pittalis; M. Segata; A. Pession; D. Santini; G. Pilu; M. Seri., Persistence of a Monosomic Cell Line in a Fetus with Mosaic Trisomy 8, «AMERICAN JOURNAL OF MEDICAL GENETICS. PART A», 2011, 155, pp. 2791 - 2794 [articolo]
Pradella LM; Zuntini R; Magini P; Ceccarelli C; Neri I; Cerasoli S; Graziano C; Gasparre G; Turchetti D, Two distinct thyroid tumours in a Cowden Syndrome patient carrying both a 10q23 and a mitochondrial DNA germline deletion, «JOURNAL OF MEDICAL GENETICS», 2011, 48(11), pp. 779 - 782 [articolo]
Cortesi, Laura; Masini, Cristina; Cirilli, Claudia; Medici, Veronica; Marchi, Isabella; Cavazzini, Giovanna; Pasini, Giuseppe; Turchetti, Daniela; Federico, Massimo, Favourable ten-year overall survival in a Caucasian population with high probability of hereditary breast cancer, «BMC CANCER», 2010, 10, Article number: 90, pp. 90 - 90 [articolo]
Bruno W.; Ghiorzo P.; Battistuzzi L.; Ascierto P.A.; Barile M.; Gargiulo S.; Gensini F.; Gliori S.; Guida M.; Lombardo M.; Manoukian S.; Menin C.; Nasti S.; Origone P. Pasini B.; Pastorino L.; Peissel B.; Pizzichetta M.A.; Queirolo P.; Rodolfo M.; Romanini A.; Scaini M.C.; Testori A.; Tibiletti M.G.; Turchetti D.; Leachman S.A.; Bianchi Scarrà G.; IMI; Italian Melanoma Intergroup., Clinical genetic testing for familial melanoma in Italy: a cooperative study, «JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY», 2009, 61, pp. 775 - 782 [articolo]
Garavelli L.; Zollino M.; Cerruti Mainardi P.; Gurrieri F.; Rivieri F.; Soli F.; Verri R.; Albertini E.; Favaron E.; Zignani M.; Orteschi D.; Bianchi P.; Faravelli F.; Forzano F.; Seri M.; Wischmeijer A.; Turchetti D.; Pompilii E.; Gnoli M.; Cocchi G.; Mazzanti L.; Bergamaschi R.; De Brasi D.; Sperandeo M.P.; Mari F.; Uliana V.; Mostardini R.; Cecconi M.; Grasso M.; Sassi S.; Sebastio G.; Renieri A.; Silengo M.; Bernasconi S.; Wakamatsu N.; Neri G., Mowat-Wilson syndrome: Facial phenotype changing with age: Study of 19 Italian patients and review of the literature, «AMERICAN JOURNAL OF MEDICAL GENETICS. PART A», 2009, 149A, pp. 417 - 426 [articolo]
