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Neurology|November 26, 2003
Intergenerational instability and marked anticipation in SCA-17F Maltecca, A Filla, I Castaldo, et al.Neurology|February 11, 2000
Atypical Friedreich ataxia phenotype associated with a novel missense mutation in the X25 geneG De Michele, A Filla, F Cavalcanti, et al.European Journal of Neurology|March 18, 2011
Myelinated retinal fibers in autosomal recessive spastic ataxia of Charlevoix-SaguenayE M Vingolo, R Di Fabio, S Salvatore, et al.Journal of Neurology|July 10, 1999
Why do some Friedreich's ataxia patients retain tendon reflexes? A clinical, neurophysiological and molecular studyG Coppola, G De Michele, F Cavalcanti, et al.Cell|July 11, 1998
Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloproteaseG Casari, M De Fusco, S Ciarmatori, et al.European Neurology|July 15, 2000
Relative frequencies of CAG expansions in spinocerebellar ataxia and dentatorubropallidoluysian atrophy in 116 Italian familiesA Filla, C Mariotti, G Caruso, et al.Human Molecular Genetics|August 1, 1997
The Friedreich ataxia GAA triplet repeat: premutation and normal allelesL Montermini, E Andermann, M Labuda, et al.Journal of Neurology|August 4, 1999
Spinocerebellar ataxia type 2 in southern Italy: a clinical and molecular study of 30 familiesA Filla, G De Michele, L Santoro, et al.European Journal of Neurology|March 21, 2020
Monogenic cerebral small-vessel diseases: diagnosis and therapy. Consensus recommendations of the European Academy of NeurologyM Mancuso, M Arnold, A Bersano, et al.Journal of Neurology|November 5, 2015
Powerhouse failure and oxidative damage in autosomal recessive spastic ataxia of Charlevoix-SaguenayChiara Criscuolo, C Procaccini, M C Meschini, et al.Pageof 13