The Mitochondrial Dysfunction Hypothesis in Autism Spectrum Disorders: Current Status and Future Perspectives

Por Citrigno, Luigi, Muglia, Maria, Qualtieri, Antonio, Spadafora, Patrizia, Cavalcanti, Francesca, Pioggia, Giovanni, Cerasa, Antonio
Publicado no Int J Mol Sci (2020)

A rare association between multiple sclerosis and Charcot‐Marie‐Tooth type 1B

Por Cortese, Rosa, Zoccolella, Stefano, Muglia, Maria, Patitucci, Alessandra, Scarafino, Antonio, Paolicelli, Damiano, Simone, Isabella Laura
Publicado no Brain Behav (2016)

A novel founder mutation in the MFN2 gene associated with variable Charcot–Marie–Tooth type 2 phenotype in two families from Southern Italy

Por Muglia, Maria, Vazza, Giovanni, Patitucci, Alessandra, Milani, Micaela, Pareyson, Davide, Taroni, Franco, Quattrone, Aldo, Mostacciuolo, Maria Luisa
Publicado em 2009

5-HTTLPR, anxiety and gender interaction moderates right amygdala volume in healthy subjects

Por Cerasa, Antonio, Quattrone, Aldo, Piras, Fabrizio, Mangone, Graziella, Magariello, Angela, Fagioli, Sabrina, Girardi, Paolo, Muglia, Maria, Caltagirone, Carlo, Spalletta, Gianfranco
Publicado em 2014

SMN1 gene copy number analyses for SMA healthy carriers in Italian population

Por Patitucci, Alessandra, Magariello, Angela, Ungaro, Carmine, Muglia, Maria, Conforti, Francesca L., Gabriele, Anna L., Citrigno, Luigi, Sproviero, William, Mazzei, Rosalucia
Publicado no J Pediatr Genet (2012)

ALS and CHARGE syndrome: a clinical and genetic study

Por Ungaro, Carmine, Citrigno, Luigi, Trojsi, Francesca, Sprovieri, Teresa, Gentile, Giulia, Muglia, Maria, Monsurrò, Maria Rosaria, Tedeschi, Gioacchino, Cavallaro, Sebastiano, Conforti, Francesca Luisa
Publicado no Acta Neurol Belg (2018)

Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case report

Por Sprovieri, Teresa, Ungaro, Carmine, Sivo, Serena, Quintiliani, Michela, Contaldo, Ilaria, Veredice, Chiara, Citrigno, Luigi, Muglia, Maria, Cavalcanti, Francesca, Cavallaro, Sebastiano, Mercuri, Eugenio, Battaglia, Domenica
Publicado no BMC Med Genet (2019)

NeuroArray: A Customized aCGH for the Analysis of Copy Number Variations in Neurological Disorders

Por La Cognata, Valentina, Morello, Giovanna, Gentile, Giulia, Cavalcanti, Francesca, Cittadella, Rita, Conforti, Francesca Luisa, De Marco, Elvira Valeria, Magariello, Angela, Muglia, Maria, Patitucci, Alessandra, Spadafora, Patrizia, D’Agata, Velia, Ruggieri, Martino, Cavallaro, Sebastiano
Publicado no Curr Genomics (2018)

Sporadic ALS is not associated with VAPB gene mutations in Southern Italy

Por Conforti, Francesca Luisa, Sprovieri, Teresa, Mazzei, Rosalucia, Ungaro, Carmine, Tessitore, Alessandro, Tedeschi, Gioacchino, Patitucci, Alessandra, Magariello, Angela, Gabriele, AnnaLia, Labella, Vincenzo, Simone, Isabella Laura, Majorana, Giovanni, Monsurrò, Maria Rosaria, Valentino, Paola, Muglia, Maria, Quattrone, Aldo
Publicado em 2006