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Italian Journal of Neurological Sciences|August 10, 2000
Cerebellar ataxia, hypogonadism and chorioretinopathy: molecular analysis of an Italian familyR Rizzi, V Carelli, L Monari, et al.Journal of Neurology, Neurosurgery, and Psychiatry|December 1, 1989
Late onset recessive ataxia with Friedreich's disease phenotypeG De Michele, A Filla, F Barbieri, et al.Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1990
Clinical and genetic heterogeneity in early onset cerebellar ataxia with retained tendon reflexesA Filla, G De Michele, F Cavalcanti, et al.Rivista Di Neurologia|March 1, 1989
[Chronic experimentation with TRH administered intramuscularly in spinocerebellar degeneration. Double-blind cross-over study in 30 subjects]A Filla, G De Michele, L Di Martino, et al.Muscle & Nerve|June 1, 1990
Electrophysiological and histological follow-up study in 15 Friedreich's ataxia patientsL Santoro, A Perretti, C Crisci, et al.Journal of Neural Transmission. Supplementum|January 1, 1995
A genetic study of Parkinson's diseaseG De Michele, A Filla, R Marconi, et al.Journal of the Neurological Sciences|June 10, 1998
Determinants of cognitive disorders in Autosomal Dominant Cerebellar Ataxia type 1L Trojano, L Chiacchio, D Grossi, et al.Rivista Di Neurologia|November 1, 1987
[Computerized tomography in the study of degenerative ataxia]G De Michele, A Filla, E Mansi, et al.Neurology|March 29, 2006
Electrophysiologic characterization in spinocerebellar ataxia 17F Manganelli, A Perretti, M Nolano, et al.Journal of Neurochemistry|February 1, 1986
Glutamate dehydrogenase in human brain: regional distribution and propertiesA Filla, G De Michele, V Brescia Morra, et al.Pageof 21