LIMONGELLI, GIUSEPPE ANTONIO
LIMONGELLI, GIUSEPPE ANTONIO
Current use of cardiac magnetic resonance in tertiary referral centres for the diagnosis of cardiomyopathy: the ESC EORP Cardiomyopathy/Myocarditis Registry
2021 Mizia-Stec, Katarzyna; Charron, Philippe; Gimeno Blanes, Juan Ramon; Elliott, Perry; Kaski, Juan Pablo; Maggioni, Aldo P; Tavazzi, Luigi; Tendera, Michał; Felix, Stephan B; Dominguez, Fernando; Ojrzynska, Natalia; Losi, Maria-Angela; Limongelli, Giuseppe; Barriales-Villa, Roberto; Seferovic, Petar M; Biagini, Elena; Wybraniec, Maciej; Laroche, Cecile; Caforio, Alida L P
Diagnosis and Management of Rare Cardiomyopathies in Adult and Paediatric Patients. A Position Paper of the Italian Society of Cardiology (SIC) and Italian Society of Paediatric Cardiology (SICP)
2022 Limongelli, Giuseppe; Adorisio, Rachele; Baggio, Chiara; Bauce, Barbara; Biagini, Elena; Castelletti, Silvia; Favilli, Silvia; Imazio, Massimo; Lioncino, Michele; Merlo, Marco; Monda, Emanuele; Olivotto, Iacopo; Parisi, Vanda; Pelliccia, Francesco; Basso, Cristina; Sinagra, Gianfranco; Indolfi, Ciro; Autore, Camillo
Molecular insight into mitochondrial DNA depletion syndrome in two patients with novel mutations in the deoxyguanosine kinase and thymidine kinase 2 genes
2005 Wang, L.; Limongelli, A.; Vila, M. R.; Carrara, F.; Zeviani, M.; Eriksson, S.
Mutation in AAC2, equivalent to human adPEO-associated ANT1 mutations, lead to defective oxidative phosphorylation in Saccharomyces cerevisiae and affect mitochondrial DNA stability
2004 Fontanesi, F.; Palmieri, L.; Scarcia, P.; Lodi, T.; Donnini, C.; Limongelli, A.; Tiranti, V.; Zeviani, M.; Ferrero, I.; Viola, A. M.
Variable penetrance of a familial progressive necrotising encephalopathy due to a novel tRNA(Ile) homoplasmic mutation in the mitochondrial genome
2004 Limongelli, A; Schaefer, J; Jackson, S; Invernizzi, F; Kirino, Y; Suzuki, T; Reichmann, H; Zeviani, M