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I Castaldo

Showing results (11-20 of 17) with videos related to

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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.
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.
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.
Neurology|November 26, 2003
Intergenerational instability and marked anticipation in SCA-17F Maltecca, A Filla, I Castaldo, 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.
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.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
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.
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.
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.
Neurology|November 26, 2003
Intergenerational instability and marked anticipation in SCA-17F Maltecca, A Filla, I Castaldo, 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.
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.
Pageof 2