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Journal of Medical Genetics|February 1, 1994
Linkage disequilibrium between FD1-D9S202 haplotypes and the Friedreich's ataxia locus in a central-southern Italian populationL Pianese, S Cocozza, G Campanella, et al.Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|May 29, 2000
Influence of GAA expansion size and disease duration on central nervous system impairment in Friedreich's ataxia: contribution to the understanding of the pathophysiology of the diseaseL Santoro, A Perretti, B Lanzillo, et al.American Journal of Human Genetics|June 23, 1998
A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3G De Michele, M De Fusco, F Cavalcanti, et al.Journal of Neurology|January 1, 1993
Evidence of a genetic marker associated with early onset in Friedreich's ataxiaS Cocozza, A Antonelli, G Campanella, et al.Acta Neurologica|August 1, 1992
Early onset hereditary ataxias of unknown etiology. Review of a personal seriesA Filla, G De Michele, F Barbieri, 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.Neurology|March 27, 2002
Early onset autosomal dominant dementia with ataxia, extrapyramidal features, and epilepsyA Filla, G De Michele, S Cocozza, 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.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.Pageof 21