Showing results (371-380 of 946) with videos related to
Sort By:
Pageof 95
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|April 1, 1986
Loss of striatal [76Br]bromospiperone binding sites demonstrated by positron tomography in progressive supranuclear palsyJ C Baron, B Mazière, C Loc'h, et al.Brain Research|April 11, 1994
Sulfonylurea binding sites in normal human brain and in Parkinson's disease, progressive supranuclear palsy and Huntington's diseaseS Holemans, F Javoy-Agid, Y Agid, et al.Annals of Neurology|February 28, 2001
14-3-3 protein cerebrospinal fluid detection in human growth hormone-treated Creutzfeldt-Jakob disease patientsJ P Brandel, K Peoc'h, P Beaudry, et al.Annals of Neurology|December 1, 1995
Striatal dopaminergic denervation in pallidopyramidal disease demonstrated by positron emission tomographyP Remy, H Hosseini, J D Degos, et al.American Journal of Medical Genetics|October 9, 1995
SCA2 is not a major locus for ADCA type I in French familiesG Cancel, G Stevanin, A Dürr, et al.Neuroscience|August 1, 1994
Somatostatin messenger RNA-containing neurons in Alzheimer's disease: an in situ hybridization study in hippocampus, parahippocampal cortex and frontal cortexP Dournaud, P Cervera-Pierot, E Hirsch, et al.Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1987
Brain somatostatin concentrations do not decrease in progressive supranuclear palsyJ Epelbaum, F Javoy-Agid, E Hirsch, et al.The European Journal of Neuroscience|December 1, 1996
DA uptake sites, D1 and D2 receptors, D2 and preproenkephalin mRNAs and Fos immunoreactivity in rat striatal subregions after partial dopaminergic degenerationM Chritin, V Blanchard, R Raisman-Vozari, et al.Neuroreport|March 3, 1997
An immunocytochemical study of a G-protein-gated inward rectifier K+ channel (GIRK2) in the weaver mouse mesencephalonC Adelbrecht, M G Murer, I Lauritzen, et al.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.Pageof 95