Showing results (301-310 of 558) with videos related to
Sort By:
Pageof 56
Clinical Neuroscience (New York, N.Y.)|January 1, 1995
Autosomal dominant cerebellar ataxia type I linked to chromosome 12q (SCA2: spinocerebellar ataxia type 2)A Dürr, A Brice, A Lepage-Lezin, et al.Annals of Neurology|February 1, 1995
Analysis of the SCA1 CAG repeat in a large number of families with dominant ataxia: clinical and molecular correlationsO Dubourg, A Dürr, G Cancel, et al.Neuroscience Letters|June 15, 1984
Cortical cholinergic projections from the basal forebrain of the rat, with special reference to the prefrontal cortex innervationW Mayo, B Dubois, A Ploska, et al.Journal of Neurochemistry|August 1, 1993
Cellular quantification of tyrosine hydroxylase in the rat brain by immunoautoradiographyV Blanchard, R Raisman-Vozari, M Savasta, et al.European Journal of Pharmacology|November 8, 1988
[3H]GBR 12935 binding to dopamine uptake sites: subcellular localization and reduction in Parkinson's disease and progressive supranuclear palsyJ M Maloteaux, M A Vanisberg, C Laterre, et al.Neuroreport|October 6, 1997
Nuclear translocation of NF-kappaB in cholinergic neurons of patients with Alzheimer's diseaseF Boissière, S Hunot, B Faucheux, et al.Experimental Brain Research|June 18, 1998
Effects of anterior cingulate cortex lesions on ocular saccades in humansB Gaymard, S Rivaud, J F Cassarini, et al.Clinical Neuropharmacology|May 14, 1998
Attentional deficits in Parkinson's disease: partial reversibility with naphtoxazine (SDZ NVI-085), a selective noradrenergic alpha 1 agonistM A Bédard, F el Massioui, C Malapani, et al.Neuroreport|May 9, 1995
Congruent unilateral impairments for real and imagined hand movementsA Sirigu, L Cohen, J R Duhamel, et al.Brain : a Journal of Neurology|December 1, 1993
Phenotypic variability in autosomal dominant cerebellar ataxia type I is unrelated to genetic heterogeneityA Dürr, H Chneiweiss, C Khati, et al.Pageof 56