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Annals of Neurology|May 1, 1996
A novel point mutation in the McLeod syndrome gene in neuroacanthocytosisM F Ho, R M Chalmers, M B Davis, et al.The Quarterly Journal of Medicine|October 1, 1993
Smoking and mitochondrial function: a model for environmental toxinsP R Smith, J M Cooper, G G Govan, et al.Brain : a Journal of Neurology|June 1, 1990
Familial cerebral amyloid angiopathy with nonneuritic amyloid plaque formationG T Plant, T Révész, R O Barnard, et al.Journal of Neurology, Neurosurgery, and Psychiatry|September 1, 1993
A familial disorder associated with palatal myoclonus, other brainstem signs, tetraparesis, ataxia and Rosenthal fibre formationR S Howard, R Greenwood, J Gawler, et al.Journal of the Neurological Sciences|November 1, 1994
HLA class II genotypes in Leber's hereditary optic neuropathyG G Govan, P R Smith, H Kellar-Wood, et al.Lancet (London, England)|June 1, 1991
Mitochondrial encephalopathies: molecular genetic diagnosis from blood samplesS R Hammans, M G Sweeney, M Brockington, et al.Brain : a Journal of Neurology|October 6, 1997
Cortical control of movement in Huntington's disease. A PET activation studyR A Weeks, A Ceballos-Baumann, P Piccini, et al.Human Molecular Genetics|March 1, 1996
Dopa-responsive dystonia in British patients: new mutations of the GTP-cyclohydrolase I gene and evidence for genetic heterogeneityO Bandmann, T G Nygaard, R Surtees, et al.Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1988
Leukocyte glutamate dehydrogenase activity in patients with degenerative neurological disordersD Aubby, H K Saggu, P Jenner, et al.Annals of Neurology|March 1, 1995
A new mitochondrial DNA mutation associated with progressive dementia and chorea: a clinical, pathological, and molecular genetic studyI Nelson, M G Hanna, N Alsanjari, et al.Pageof 21