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Journal of Neurology|July 1, 1992

Prevalence of hereditary ataxias and spastic paraplegias in Molise, a region of ItalyA Filla, G De Michele, R Marconi, et al.

Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1994

Late onset Friedreich's disease: clinical features and mapping of mutation to the FRDA locusG De Michele, A Filla, F Cavalcanti, et al.

Cerebellum (London, England)|August 31, 2019

The Working Life of People with Degenerative Cerebellar AtaxiaA Ranavolo, M Serrao, T Varrecchia, et al.

Neurology|March 27, 2002

Early onset autosomal dominant dementia with ataxia, extrapyramidal features, and epilepsyA Filla, G De Michele, S Cocozza, et al.

Journal of Medical Genetics|August 14, 2008

DNA methylation in intron 1 of the frataxin gene is related to GAA repeat length and age of onset in Friedreich ataxia patientsI Castaldo, M Pinelli, A Monticelli, et al.

Neurology|December 31, 1997

Broadened Friedreich's ataxia phenotype after gene cloning. Minimal GAA expansion causes late-onset spastic ataxiaM Ragno, G De Michele, F Cavalcanti, et al.

The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|June 2, 2006

Cervico-oculo-Acoustic syndrome in a male with consanguineous parentsL Di Maio, V Marcelli, C Vitale, et al.

Neurology|January 14, 2004

A novel mutation in SACS gene in a family from southern ItalyC Criscuolo, S Banfi, M Orio, et al.

Journal of the Neurological Sciences|October 1, 1996

Autosomal dominant cerebellar ataxia type I. Clinical and molecular study in 36 Italian families including a comparison between SCA1 and SCA2 phenotypesA Filla, G De Michele, G Campanella, et al.

Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 5, 2003

Dementia, ataxia, extrapyramidal features, and epilepsy: phenotype spectrum in two Italian families with spinocerebellar ataxia type 17G De Michele, F Maltecca, M Carella, et al.

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Showing results (81-90 of 130) with videos related to

Sort By:

Pageof 13

Journal of Neurology|July 1, 1992

Prevalence of hereditary ataxias and spastic paraplegias in Molise, a region of ItalyA Filla, G De Michele, R Marconi, et al.

Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1994

Late onset Friedreich's disease: clinical features and mapping of mutation to the FRDA locusG De Michele, A Filla, F Cavalcanti, et al.

Cerebellum (London, England)|August 31, 2019

The Working Life of People with Degenerative Cerebellar AtaxiaA Ranavolo, M Serrao, T Varrecchia, et al.

Neurology|March 27, 2002

Early onset autosomal dominant dementia with ataxia, extrapyramidal features, and epilepsyA Filla, G De Michele, S Cocozza, et al.

Journal of Medical Genetics|August 14, 2008

DNA methylation in intron 1 of the frataxin gene is related to GAA repeat length and age of onset in Friedreich ataxia patientsI Castaldo, M Pinelli, A Monticelli, et al.

Neurology|December 31, 1997

Broadened Friedreich's ataxia phenotype after gene cloning. Minimal GAA expansion causes late-onset spastic ataxiaM Ragno, G De Michele, F Cavalcanti, et al.

The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|June 2, 2006

Cervico-oculo-Acoustic syndrome in a male with consanguineous parentsL Di Maio, V Marcelli, C Vitale, et al.

Neurology|January 14, 2004

A novel mutation in SACS gene in a family from southern ItalyC Criscuolo, S Banfi, M Orio, et al.

Journal of the Neurological Sciences|October 1, 1996

Autosomal dominant cerebellar ataxia type I. Clinical and molecular study in 36 Italian families including a comparison between SCA1 and SCA2 phenotypesA Filla, G De Michele, G Campanella, et al.

Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 5, 2003

Dementia, ataxia, extrapyramidal features, and epilepsy: phenotype spectrum in two Italian families with spinocerebellar ataxia type 17G De Michele, F Maltecca, M Carella, et al.

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