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Journal of Neurology, Neurosurgery, and Psychiatry|February 1, 1996
Autosomal dominant optic atrophy with asymptomatic peripheral neuropathyR M Chalmers, A C Bird, A E HardingAnnals of Neurology|August 1, 1996
Sequence of mitochondrial DNA in patients with multiple sclerosisR M Chalmers, N Robertson, DAS Compston, et al.Journal of the Neurological Sciences|February 1, 1996
HLA class I genotypes in Leber's hereditary optic neuropathyR M Chalmers, G G Govan, A H Schapira, et al.Journal of Neurology|May 1, 1995
Sequence of the human homologue of a mitochondrially encoded murine transplantation antigen in patients with multiple sclerosisR M Chalmers, N Robertson, H Kellar-Wood, et al.American Journal of Human Genetics|July 1, 1996
Evidence against an X-linked visual loss susceptibility locus in Leber hereditary optic neuropathyR M Chalmers, M B Davis, M G Sweeney, et al.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.Journal of the Neurological Sciences|November 1, 1996
Mitochondrial encephalopathy with multiple mitochondrial DNA deletions: a report of two families and two sporadic cases with unusual clinical and neuropathological featuresR M Chalmers, M Brockington, R S Howard, et al.Neurology|August 1, 1997
A mitochondrial DNA tRNA(Val) point mutation associated with adult-onset Leigh syndromeR M Chalmers, P J Lamont, I Nelson, et al.Parasite (Paris, France)|September 26, 2008
Cryptosporidium: from laboratory diagnosis to surveillance and outbreaksR M ChalmersJournal of Neurology, Neurosurgery, and Psychiatry|October 1, 1981
Hereditary "pure" spastic paraplegia: a clinical and genetic study of 22 familiesA E HardingPageof 56