Elena Ronchetti

Biologo

napolitano c., schwartz p.j., brown a.m., ronchetti e., bianchi l., pinnavia a., acquaro g. and priori s.g. evidence for cardiac ion-channel mutation underlyng drug-induced torsades de pointes. j cardiovasc electrophysiol.691-696, vol 11, no 6, june 2000 , futura publishing company , armonk ny , usa.

priori s., ronchetti e., memmi m. gene specific therapy for arrythmogenic disorders. ital. heart j. 2000; 1 (suppl3): s52-s54.

priori s.g., napolitano c., schwartz p.j., bloise r., crotti l., ronchetti e. the elusive link between lqt3 and brugada syndrome. the role of flecainide challenge. circulation.2000; 102:945-947.

shwartz p.j., priori s.g., bloise r., napolitano c., ronchetti e., piccinini a., goj c., breithardt g., shulze-bhar e., wedekind h., nastoli j. molecular diagnosis in a child with sudden infant death syndrome. the lancet, 2001 vol.358 1342-1343

priori s.g, schwartz p.j., napolitano c., bloise r., ronchetti e., grillo m., vicentini a., spazzolini c., nastoli j., bottelli g., folli r., cappelletti d., risk stratification in the long-qt syndrome. the new england journal of medecine may 2003; 348:1866-74

priori sg, napolitano c, schwartz pj, grillo m, bloise r, ronchetti e, moncalvo c, tulipani c, veia a, bottelli g, nastoli j. association of long qt syndrome loci and cardiac events among patients treated with beta-blockers. jama. 2004 sep 15;292(11):1341-4.

priori sg, schwartz pj, napolitano c, bloise r, ronchetti e, grillo m, vicentini a, spazzolini c, nastoli j, bottelli g, folli r, cappelletti d.  risk stratification in the long-qt syndrome. n engl j med. 2003 may 8;348(19):1866-74

napolitano c, priori sg, schwartz pj, bloise r, ronchetti e, nastoli j, bottelli g, cerrone m, leonardi s.. genetic testing in the long qt syndrome: development and validation of an efficient approach to genotyping in clinical practice. 2005 dec 21;294(23):2975-80

priori sg, pandit sv, rivolta i, berenfeld o, ronchetti e, dhamoon a, napolitano c, anumonwo j, di barletta mr, gudapakkam s, bosi g, stramba-badiale m, jalife j. a novel form of short qt syndrome (sqt3) is caused by a mutation in the kcnj2 gene. circ res. 2005 apr 15;96(7):800-7.

genetic testing in the long qt syndrome: development and validation of an efficient approach to genotyping in clinical practice. napolitano c, priori sg, schwartz pj, bloise r, ronchetti e, nastoli j, bottelli g, cerrone m, leonardi s. jama. 2005 dec 21;294(23):2975-80.

beltrame l1, di marino m1, fruscio r2, calura e3, chapman b4, clivio l1, sina f2, mele c5, iatropoulos p5, grassi t2, fotia v6, romualdi c3, martini p3, noris m5, paracchini l1, craparotta i1, petrillo m7, milani r2, perego p8, ravaggi a9, zambelli a10, ronchetti e11, d'incalci m12, marchini s1. profiling cancer gene mutations in longitudinal epithelial ovarian cancer biopsies by targeted next-generation sequencing: a retrospective study. ann oncol. 2015 apr 6. pii: mdv164. [epub ahead of print]