MicroRNAs are appropriate in mitochondrial related hearing loss? Answer to the skepticism

Por Arianna Di Stadio, Corrado Angelini
Publicado em 2018-07-01

Characterization of two ETFDH mutations in a novel case of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency

Por Sara Missaglia, Daniela Tavian, Laura Moro, Corrado Angelini
Publicado em 2018-11-01

Correlation between ETFDH mutations and dysregulation of serum myomiRs in MADD patients

Por Sara Missaglia, Valentina Pegoraro, Roberta Marozzo, Daniela Tavian, Corrado Angelini
Publicado em 2020-03-01

Integrated care of muscular dystrophies in Italy. Part 2. Psychological treatments, social and welfare support, and financial costs

Por Lorenza, Magliano, Marianna, Scutifero, Melania, Patalano, Alessandra, Sagliocchi, Antonella, Zaccaro, Federica, Civati, Erika, Brighina, Gianluca, Vita, Sonia, Messina, Maria, Sframeli, Maria_Elena, Lombardo, Roberta, Scalise, Giulia, Colia, Maria, Catteruccia, Angela, Berardinelli, Maria_Chiara, Motta, Alessandra, Gaiani, Claudio, Semplicini, Luca, Bello, Guja, Astrea, Giulia, Ricci, Maria_Grazia, D'Angelo, Giuseppe, Vita, Marika, Pane, Adele, D'Amico, Umberto, Balottin, Corrado, Angelini, Roberta, Battini, Luisa, Politano
Publicado no Acta Myol (2017)

Interpretation of the Epigenetic Signature of Facioscapulohumeral Muscular Dystrophy in Light of Genotype-Phenotype Studies

Por Ana Nikolic, Takako I Jones, Monica Govi, Fabiano Mele, Louise Maranda, Francesco Sera, Giulia Ricci, Lucia Ruggiero, Liliana Vercelli, Simona Portaro, Luisa Villa, Chiara Fiorillo, Lorenzo Maggi, Lucio Santoro, Giovanni Antonini, Massimiliano Filosto, Maurizio Moggio, Corrado Angelini, Elena Pegoraro, Angela Berardinelli, Maria Antonetta Maioli, Grazia D’Angelo, Antonino Di Muzio, Gabriele Siciliano, Giuliano Tomelleri, Maurizio D’Esposito, Floriana Della Ragione, Arianna Brancaccio, Rachele Piras, Carmelo Rodolico, Tiziana Mongini, Frederique Magdinier, Valentina Salsi, Peter L. Jones, Rossella Tupler
Publicado em 2020-04-01