1. 245 Arrhythmogenic cardiomyopathy in children according to 'padua criteria': single paediatric centre experience. (8th December 2021) Authors: Cicenia, Marianna; Cantarutti, Nicoletta; Adorisio, Rachele; Silvetti, Massimo Stefano; Secinaro, Aurelio; Ciancarella, Paolo; Di Mambro, Corrado; Magliozzi, Monia; Novelli, Antonio; Amodeo, Antonio; Baban, Anwar; Drago, Fabrizio 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. 879 STUDY OF ATRIOVENTRICULAR CONDUCTION DEFECTS AND ARRHYTHMIAS IN PATIENTS WITH DILATATIVE CARDIOMIOPATHY CLINICAL PROGNOSTIC VALUE OF THE GENETIC ANALYSIS USING NEXT GENERATION SEQUENCING AT THREE YEARS. (15th December 2022) Authors: Campisi, Mariapaola; Di Bella, Gianluca; De Gregorio, Cesare; De Sarro, Rosalba; Luongo, Alfredo; Greco, Vittoria; Vacirca, Veronica; Luigi, Alioto; La Rosa, Maria Angela; Magliozzi, Monia; Antonio, Novelli; Silvana, Briguglia 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. 8p23.1 deletion: Look out for left ventricular hypertrabeculation and not only congenital heart diseases. Single‐center experience and literature revision. Issue 3 (13th December 2021) Authors: Cicenia, Marianna; Alesi, Viola; Orlando, Valeria; Magliozzi, Monia; Di Tommaso, Silvia; Iodice, Francesca G.; Pompei, Emanuela; Toscano, Alessandra; Digilio, Maria C.; Drago, Fabrizio; Novelli, Antonio; Baban, Anwar Journal: American journal of medical genetics Issue: Volume 188:Issue 3(2022) Page Start: 883 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Arrhythmogenic cardiomyopathy in children according to "Padua criteria": Single pediatric center experience. (1st March 2022) Authors: Cicenia, Marianna; Cantarutti, Nicoletta; Adorisio, Rachele; Silvetti, Massimo Stefano; Secinaro, Aurelio; Ciancarella, Paolo; Di Mambro, Corrado; Magliozzi, Monia; Novelli, Antonio; Amodeo, Antonio; Baban, Anwar; Drago, Fabrizio Journal: International journal of cardiology Issue: Volume 350(2022) Page Start: 83 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Clinical and molecular characterizations of 11 new patients with type 1 Feingold syndrome: Proposal for selecting diagnostic criteria and further genetic testing in patients with severe phenotype. Issue 4 (14th January 2021) Authors: Tedesco, Maria Giovanna; Lonardo, Fortunato; Ceccarini, Caterina; Cesarano, Carla; Digilio, Maria Cristina; Magliozzi, Monia; Rogaia, Daniela; Mencarelli, Amedea; Leoni, Chiara; Piscopo, Carmelo; Imperatore, Valentina; Falco, Maria Teresa; Fontana, Paolo; Nardone, Anna Maria; Novelli, Antonio; Tr... Journal: American journal of medical genetics Issue: Volume 185:Issue 4(2021) Page Start: 1204 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Cover Image, Volume 38, Issue 4. Issue 4 (April 2017) Authors: Pannone, Luca; Bocchinfuso, Gianfranco; Flex, Elisabetta; Rossi, Cesare; Baldassarre, Giuseppina; Lissewski, Christina; Pantaleoni, Francesca; Consoli, Federica; Lepri, Francesca; Magliozzi, Monia; Anselmi, Massimiliano; Delle Vigne, Silvia; Sorge, Giovanni; Karaer, Kadri; Cuturilo, Goran; Sartor... Journal: Human mutation Issue: Volume 38:Issue 4(2017) Page Start: i Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Defining the Epsilon‐Sarcoglycan (SGCE) Gene Phenotypic Signature in Myoclonus‐Dystonia: A Reappraisal of Genetic Testing Criteria. Issue 6 (15th May 2013) Authors: Carecchio, Miryam; Magliozzi, Monia; Copetti, Massimiliano; Ferraris, Alessandro; Bernardini, Laura; Bonetti, Monica; Defazio, Giovanni; Edwards, Mark J.; Torrente, Isabella; Pellegrini, Fabio; Comi, Cristoforo; Bhatia, Kailash P.; Valente, Enza Maria Journal: Movement disorders Issue: Volume 28:Issue 6(2013) Page Start: 787 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Delayed appearance of 3‐methylglutaconic aciduria in neonates with early onset metabolic cardiomyopathies: A potential pitfall for the diagnosis. Issue 1 (15th November 2019) Authors: Baban, Anwar; Adorisio, Rachele; Corica, Bernadette; Rizzo, Cristiano; Calì, Federica; Semeraro, Michela; Taurisano, Roberta; Magliozzi, Monia; Carrozzo, Rosalba; Parisi, Francesco; Dallapiccola, Bruno; Vaz, Frédéric M.; Drago, Fabrizio; Dionisi‐Vici, Carlo Journal: American journal of medical genetics Issue: Volume 182:Issue 1(2020) Page Start: 64 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. DHPLC Screening of ATM Gene in Italian Patients Affected by Ataxia-Telangiectasia: Fourteen Novel ATM Mutations. Issue 4 (9th June 2013) Authors: Magliozzi, Monia; Piane, Maria; Torrente, Isabella; Sinibaldi, Lorenzo; Rizzo, Giovanni; Savio, Camilla; Lulli, Patrizia; De Luca, Alessandro; Dallapiccola, Bruno; Chessa, Luciana Journal: Disease markers Issue: Volume 22:Issue 4(2006) Page Start: 257 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Familial aggregation of "apple peel" intestinal atresia and cardiac left‐sided obstructive lesions: A possible causal relationship with NOTCH1 gene mutations. Issue 8 (20th May 2019) Authors: Digilio, M. Cristina; Magliozzi, Monia; Di Pede, Alessandra; Valfrè, Laura; Dentici, Maria Lisa; Auriti, Cinzia; Marino, Bruno; Novelli, Antonio; Dallapiccola, Bruno Journal: American journal of medical genetics Issue: Volume 179:Issue 8(2019) Page Start: 1570 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗