1. 596 Multidisciplinary in-depth investigation in a young athlete suffering from syncope caused by myocardial bridge. (8th December 2021) Authors: Brancaccio, Mariarita; Cesaro, Arturo; Monda, Emanuele; D'Argenio, Valeria; Casaburi, Giorgio; Mazzaccara, Cristina; Limongelli, Giuseppe; Calabro, Paolo; Lombardo, Barbara; Scudiero, Olga; Frisso, Giulia Journal: European heart journal supplements Issue: Volume 23(2021)Supplement G Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. 835 CARDIOMYOPATHIES: IS IT USEFUL TO ANALYZE MINOR GENES?. (15th December 2022) Authors: Mazzaccara, Cristina; Barretta, Ferdinando; Uomo, Fabiana; Caiazza, Martina; Monda, Emanuele; Lombardi, Raffaella; Losi, Maria Angela; Limongelli, Giuseppe; D´argenio, Valeria; Frisso, Giulia Journal: European heart journal supplements Issue: Volume 24(2022)Supplement K Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A common polymorphism in the SCN5A gene is associated with dilated cardiomyopathy. Issue 7 (July 2018) Authors: Mazzaccara, Cristina; Limongelli, Giuseppe; Petretta, Mario; Vastarella, Rossella; Pacileo, Giuseppe; Bonaduce, Domenico; Salvatore, Francesco; Frisso, Giulia Journal: Journal of cardiovascular medicine Issue: Volume 19:Issue 7(2018:Jul.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Contemporary genetic testing in inherited cardiac disease: tools, ethical issues, and clinical applications. Issue 1 (January 2018) Authors: Girolami, Francesca; Frisso, Giulia; Benelli, Matteo; Crotti, Lia; Iascone, Maria; Mango, Ruggiero; Mazzaccara, Cristina; Pilichou, Kalliope; Arbustini, Eloisa; Tomberli, Benedetta; Limongelli, Giuseppe; Basso, Cristina; Olivotto, Iacopo Journal: Journal of cardiovascular medicine Issue: Volume 19:Issue 1(2018:Jan.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. First trimester ultrasound features of X-linked Opitz syndrome and early molecular diagnosis: case report and review of the literature. (17th September 2021) Authors: Sarno, Laura; Maruotti, Giuseppe Maria; Izzo, Antonella; Mazzaccara, Cristina; Carbone, Luigi; Esposito, Giuseppina; Di Cresce, Marco; Saccone, Gabriele; Sirico, Angelo; Genesio, Rita; Mollo, Nunzia; Martinelli, Pasquale; Conti, Anna; Zullo, Fulvio; Frisso, Giulia Journal: Journal of maternal-fetal & neonatal medicine Issue: Volume 34:Number 18(2021) Page Start: 3089 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genetic analysis resolves differential diagnosis of a familial syndromic dilated cardiomyopathy: A new case of Alström syndrome. Issue 7 (12th May 2020) Authors: Lombardo, Barbara; D'Argenio, Valeria; Monda, Emanuele; Vitale, Andrea; Caiazza, Martina; Sacchetti, Lucia; Pastore, Lucio; Limongelli, Giuseppe; Frisso, Giulia; Mazzaccara, Cristina Journal: Molecular genetics & genomic medicine Issue: Volume 8:Issue 7(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Mild dehydration in dyspeptic athletes is able to increase gastrointestinal symptoms: Protective effects of an appropriate hydration. Issue 1 (16th December 2018) Authors: Zito, Francesco Paolo; Gala, Antonietta; Genovese, Daniela; Vozzella, Letizia; Polese, Barbara; Cassarano, Sara; Cargiolli, Martina; Andreozzi, Paolo; Gelzo, Monica; Sarnelli, Giovanni; Frisso, Giulia; Cuomo, Rosario Journal: Neurogastroenterology & motility Issue: Volume 31:Issue 1(2019) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Mulibrey nanism: Two novel mutations in a child identified by Array CGH and DNA sequencing. Issue 8 (3rd June 2016) Authors: Mozzillo, Enza; Cozzolino, Carla; Genesio, Rita; Melis, Daniela; Frisso, Giulia; Orrico, Ada; Lombardo, Barbara; Fattorusso, Valentina; Discepolo, Valentina; Della Casa, Roberto; Simonelli, Francesca; Nitsch, Lucio; Salvatore, Francesco; Franzese, Adriana Journal: American journal of medical genetics Issue: Volume 170:Issue 8(2016) Page Start: 2196 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Prevalence and clinical significance of red flags in patients with hypertrophic cardiomyopathy. (15th January 2020) Authors: Limongelli, Giuseppe; Monda, Emanuele; Tramonte, Stefania; Gragnano, Felice; Masarone, Daniele; Frisso, Giulia; Esposito, Augusto; Gravino, Rita; Ammendola, Ernesto; Salerno, Gemma; Rubino, Marta; Caiazza, Martina; Russo, Mariagiovanna; Calabrò, Paolo; Elliott, Perry Mark; Pacileo, Giuseppe Journal: International journal of cardiology Issue: Volume 299(2020) Page Start: 186 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Should a BRCA2 stop codon human variant, usually considered a polymorphism, be classified as a predisposing mutation?. Issue 10 (5th February 2014) Authors: D'Argenio, Valeria; Esposito, Maria Valeria; Gilder, Jean Ann; Frisso, Giulia; Salvatore, Francesco Journal: Cancer Issue: Volume 120:Issue 10(2014) Page Start: 1594 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗