Showing results (71-80 of 123) with videos related to
Sort By:
Pageof 13
Acta Neurologica Scandinavica|September 16, 2015
SPG5 and multiple sclerosis: clinical and genetic overlap?C Criscuolo, R Carbone, M Lieto, 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.Acta Neurologica|December 1, 1989
Steroid-induced disappearance of primary central nervous system lymphoma. Clinical, neuroradiological and pathological findingsA Filla, G De Michele, F P D'Armiento, et al.European Journal of Nuclear Medicine|December 1, 1994
Ambulatory monitoring of left ventricular function in patients with Parkinson's disease and postural hypotensionA Nappi, A Cuocolo, N Iazzetta, et al.Journal of the Neurological Sciences|August 30, 2008
Autonomic nervous system abnormalities in spinocerebellar ataxia type 2: a cardiovascular neurophysiologic studyG De Joanna, A De Rosa, E Salvatore, 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.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|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.Journal of Neurology, Neurosurgery, and Psychiatry|July 20, 2007
Brain structural damage in Friedreich's ataxiaR Della Nave, A Ginestroni, M Giannelli, 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.Pageof 13