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Revue Neurologique|March 1, 1979
[Neuropathological study of adult intracranial hemorrhage. General data in 500 cases]G Boudouresques, J J Hauw, V Meininger, et al.Revue Neurologique|January 1, 1985
[Spinal forms of multiple sclerosis. Value and criticism of examination by cerebral magnetic resonance. Apropos of 4 cases]O Lyon-Caen, M T Iba-Zizen, J Tamraz, et al.Brain Research. Molecular Brain Research|November 1, 1996
Effects of L-DOPA-therapy on dopamine D2 receptor mRNA expression in the striatum of MPTP-intoxicated parkinsonian monkeysM T Herrero, S J Augood, H Asensi, et al.Neurology|April 1, 1994
Role of pontine nuclei damage in smooth pursuit impairment of progressive supranuclear palsy: a clinical-pathologic studyS Malessa, B Gaymard, S Rivaud, et al.Annals of Neurology|April 1, 1994
Eye movements in parkinsonian syndromesM Vidailhet, S Rivaud, N Gouider-Khouja, et al.Journal of Neurology, Neurosurgery, and Psychiatry|March 7, 1998
Are cognitive changes the first symptoms of Huntington's disease? A study of gene carriersV Hahn-Barma, B Deweer, A Dürr, et al.Revue Neurologique|December 1, 1995
[Phenotype of familial forms of early-onset Alzheimer's disease linked to chromosome 14. Clinical and neuropsychological characteristics of a large group]D Hannequin, D Campion, S Tardieu, et al.Annals of Neurology|May 1, 1989
Continuous and intermittent levodopa differentially affect basal ganglia functionJ L Juncos, T M Engber, R Raisman, et al.Annals of Neurology|March 20, 1998
Eye movement abnormalities correlate with genotype in autosomal dominant cerebellar ataxia type IS Rivaud-Pechoux, A Dürr, B Gaymard, et al.American Journal of Human Genetics|January 1, 1995
The gene for spinal cerebellar ataxia 3 (SCA3) is located in a region of approximately 3 cM on chromosome 14q24.3-q32.2G Stevanin, G Cancel, A Dürr, et al.Pageof 56