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Journal of the Neurological Sciences|September 15, 1996
The GTP-cyclohydrolase I gene in atypical parkinsonian patients: a clinico-genetic studyO Bandmann, S Daniel, C D Marsden, et al.Journal of the Neurological Sciences|June 1, 1995
Impaired mitochondrial translation in human myoblasts harbouring the mitochondrial DNA tRNA lysine 8344 A-->G (MERRF) mutation: relationship to proportion of mutant mitochondrial DNAM G Hanna, I P Nelson, J A Morgan-Hughes, et al.Annals of Neurology|March 1, 1992
A follow-up study of isolated cases of suspected Huntington's diseaseD Bateman, A M Boughey, F Scaravilli, et al.Annals of Neurology|May 1, 1992
Duplication of part of chromosome 17 is commonly associated with hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease type 1)P J Hallam, A E Harding, J Berciano, et al.American Journal of Human Genetics|March 1, 1990
A new mitochondrial disease associated with mitochondrial DNA heteroplasmyI J Holt, A E Harding, R K Petty, et al.Clinical Neuropathology|July 1, 1995
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)--confirmation by cerebral biopsy in 2 casesG A Lammie, J Rakshi, M N Rossor, et al.Archives of Neurology|February 1, 1992
The neuropsychological features of mitochondrial myopathies and encephalomyopathiesL D Kartsounis, D D Troung, J A Morgan-Hughes, et al.American Journal of Human Genetics|January 1, 1990
Linkage of hereditary motor and sensory neuropathy type I to the pericentromeric region of chromosome 17H R Middleton-Price, A E Harding, C Monteiro, et al.Journal of Neurology|October 1, 1995
Haplotype analysis of French, British and other European patients with familial amyloid polyneuropathy (met 30 and tyr 77)M M Reilly, D Adams, M B Davis, et al.Lancet (London, England)|September 10, 1994
Mutation analysis in patients with possible but apparently sporadic Huntington's diseaseM B Davis, D Bateman, N P Quinn, et al.Pageof 21