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American Journal of Human Genetics|September 1, 1996
The relationship between trinucleotide (GAA) repeat length and clinical features in Friedreich ataxiaA Filla, G De Michele, F Cavalcanti, et al.Human Molecular Genetics|November 13, 1998
Parental gender, age at birth and expansion length influence GAA repeat intergenerational instability in the X25 gene: pedigree studies and analysis of sperm from patients with Friedreich's ataxiaG De Michele, F Cavalcanti, C Criscuolo, et al.Journal of Neurology|April 29, 1998
Determinants of onset age in Friedreich's ataxiaG De Michele, A Filla, C Criscuolo, et al.Neuropediatrics|February 1, 1996
Childhood onset of Friedreich ataxia: a clinical and genetic study of 36 casesG De Michele, L Di Maio, A Filla, et al.Acta Neurologica|August 1, 1992
Classifications of hereditary ataxias. A critical overviewG Campanella, A Filla, G De MicheleEuropean Neurology|January 1, 1978
Smell and taste acuity in epileptic syndromesG Campanella, A Filla, G De MicheleActa Neurologica|August 1, 1992
Friedreich's disease. A linkage study in southern and central ItalyF Cavalcanti, S Cocozza, A Filla, et al.Journal of Neurology, Neurosurgery, and Psychiatry|January 14, 1999
Relation between trinucleotide GAA repeat length and sensory neuropathy in Friedreich's ataxiaL Santoro, G De Michele, A Perretti, et al.Journal of the Neurological Sciences|October 1, 1996
Autosomal dominant cerebellar ataxia type I: multimodal electrophysiological study and comparison between SCA1 and SCA2 patientsA Perretti, L Santoro, B Lanzillo, et al.European Journal of Human Genetics : EJHG|January 1, 1993
Linkage disequilibrium analysis of Friedreich's ataxia in 140 Caucasian families: positioning of the disease locus and evaluation of allelic heterogeneityG Sirugo, S Cocozza, A Brice, et al.Pageof 21