Reply to: Double trouble progressive external ophthalmoplegia and Huntington's disease

by Filosto, Massimiliano, Santorelli, Filippo M.
Published 2016

Tetracyclines and Neuromuscular Disorders

by Orsucci, Daniele, Mancuso, Michelangelo, Filosto, Massimiliano, Siciliano, Gabriele
Published 2012

Mitochondrial DNA sequence variation and neurodegeneration

by Mancuso, Michelangelo, Filosto, Massimiliano, Orsucci, Daniele, Siciliano, Gabriele
Published 2008

A complex craniovertebral junction malformation in a patient with late onset glycogenosis 2

by Cotelli, Mariasofia, Fontanella, Marco, Padovani, Alessandro, Filosto, Massimiliano
Published 2014

Mitochondrial Sensorineural Hearing Loss: A Retrospective Study and a Description of Cochlear Implantation in a MELAS Patient

by Scarpelli, Mauro, Zappini, Francesca, Filosto, Massimiliano, Russignan, Anna, Tonin, Paola, Tomelleri, Giuliano
Published 2012

May “Mitochondrial Eve” and Mitochondrial Haplogroups Play a Role in Neurodegeneration and Alzheimer's Disease?

by Ienco, Elena Caldarazzo, Simoncini, Costanza, Orsucci, Daniele, Petrucci, Loredana, Filosto, Massimiliano, Mancuso, Michelangelo, Siciliano, Gabriele
Published 2011

Small Nerve Fiber Pathology in Critical Illness

by Latronico, Nicola, Filosto, Massimiliano, Fagoni, Nazzareno, Gheza, Laura, Guarneri, Bruno, Todeschini, Alice, Lombardi, Raffaella, Padovani, Alessandro, Lauria, Giuseppe
Published 2013

Non-muscle involvement in late-onset Glycogenosis II

by FILOSTO, MASSIMILIANO, TODESCHINI, ALICE, COTELLI, MARIA SOFIA, VIELMI, VALENTINA, RINALDI, FABRIZIO, ROTA, SILVIA, SCARPELLI, MAURO, PADOVANI, ALESSANDRO
Published 2013

A novel mitochondrial tRNAAla gene variant causes chronic progressive external ophthalmoplegia in a patient with Huntington disease

by Filosto, Massimiliano, Lanzi, Gaetana, Nesti, Claudia, Vielmi, Valentina, Marchina, Eleonora, Galvagni, Anna, Giliani, Silvia, Santorelli, Filippo M., Padovani, Alessandro
Published 2016

Very Late-Onset Friedreich Ataxia with Laryngeal Dystonia

by Rota, Silvia, Marchina, Eleonora, Todeschini, Alice, Nanetti, Lorenzo, Rinaldi, Fabrizio, Vanotti, Alessandra, Mariotti, Caterina, Padovani, Alessandro, Filosto, Massimiliano
Published 2014

Poor Outcome in a Mitochondrial Neurogastrointestinal Encephalomyopathy Patient with a Novel TYMP Mutation: The Need for Early Diagnosis

by Scarpelli, Mauro, Russignan, Anna, Zombor, Melinda, Bereczki, Csaba, Zappini, Francesca, Buono, Romina, Bax, Bridget E., Padovani, Alessandro, Tonin, Paola, Filosto, Massimiliano
Published 2012

Erythropoietin in amyotrophic lateral sclerosis: a multicentre, randomised, double blind, placebo controlled, phase III study

by Lauria, Giuseppe, Dalla Bella, Eleonora, Antonini, Giovanni, Borghero, Giuseppe, Capasso, Margherita, Caponnetto, Claudia, Chiò, Adriano, Corbo, Massimo, Eleopra, Roberto, Fazio, Raffaella, Filosto, Massimiliano, Giannini, Fabio, Granieri, Enrico, La Bella, Vincenzo, Logroscino, Giancarlo, Mandrioli, Jessica, Mazzini, Letizia, Monsurrò, Maria Rosaria, Mora, Gabriele, Pietrini, Vladimiro, Quatrale, Rocco, Rizzi, Romana, Salvi, Fabrizio, Siciliano, Gabriele, Sorarù, Gianni, Volanti, Paolo, Tramacere, Irene, Filippini, Graziella
Published 2015

A novel clinical tool to classify facioscapulohumeral muscular dystrophy phenotypes

by Ricci, Giulia, Ruggiero, Lucia, Vercelli, Liliana, Sera, Francesco, Nikolic, Ana, Govi, Monica, Mele, Fabiano, Daolio, Jessica, Angelini, Corrado, Antonini, Giovanni, Berardinelli, Angela, Bucci, Elisabetta, Cao, Michelangelo, D’Amico, Maria Chiara, D’Angelo, Grazia, Di Muzio, Antonio, Filosto, Massimiliano, Maggi, Lorenzo, Moggio, Maurizio, Mongini, Tiziana, Morandi, Lucia, Pegoraro, Elena, Rodolico, Carmelo, Santoro, Lucio, Siciliano, Gabriele, Tomelleri, Giuliano, Villa, Luisa, Tupler, Rossella
Published 2016

Genotype-phenotype correlation in Pompe disease, a step forward

by De Filippi, Paola, Saeidi, Kolsoum, Ravaglia, Sabrina, Dardis, Andrea, Angelini, Corrado, Mongini, Tiziana, Morandi, Lucia, Moggio, Maurizio, Di Muzio, Antonio, Filosto, Massimiliano, Bembi, Bruno, Giannini, Fabio, Marrosu, Giovanni, Rigoldi, Miriam, Tonin, Paola, Servidei, Serenella, Siciliano, Gabriele, Carlucci, Annalisa, Scotti, Claudia, Comelli, Mario, Toscano, Antonio, Danesino, Cesare
Published 2014

Large scale genotype–phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophy

by Ricci, Giulia, Scionti, Isabella, Sera, Francesco, Govi, Monica, D’Amico, Roberto, Frambolli, Ilaria, Mele, Fabiano, Filosto, Massimiliano, Vercelli, Liliana, Ruggiero, Lucia, Berardinelli, Angela, Angelini, Corrado, Antonini, Giovanni, Bucci, Elisabetta, Cao, Michelangelo, Daolio, Jessica, Di Muzio, Antonio, Di Leo, Rita, Galluzzi, Giuliana, Iannaccone, Elisabetta, Maggi, Lorenzo, Maruotti, Valerio, Moggio, Maurizio, Mongini, Tiziana, Morandi, Lucia, Nikolic, Ana, Pastorello, Ebe, Ricci, Enzo, Rodolico, Carmelo, Santoro, Lucio, Servida, Maura, Siciliano, Gabriele, Tomelleri, Giuliano, Tupler, Rossella
Published 2013