Pubblicazioni

Uniparental disomy of chromosome 1 unmasks recessive mutations of PPT1 in a boy with neuronal ceroid lipofuscinosis type 1

2017 - BRAIN & DEVELOPMENT
Travaglini, Lorena; Aiello, Chiara; Alesi, Viola; Loddo, Sara; Novelli, Antonio; Tozzi, Giulia; Bertini, Enrico; Leuzzi, Vincenzo; Brancati, Francesco

Remarks about “a pediatric patient of hemorrhagic acute transverse myelitis”

2017 - BRAIN & DEVELOPMENT
Coraci, Daniele; Santilli, Valter; Giovannini, Silvia; Padua, Luca

Infantile neuroaxonal dystrophy and PLA2G6-associated neurodegeneration: An update for the diagnosis

2017 - BRAIN & DEVELOPMENT
Iodice, A.; Spagnoli, C.; Salerno, G. G.; Frattini, D.; Bertani, G.; Bergonzini, P.; Pisani, F.; Fusco, C.

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