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The Quarterly Journal of Medicine|January 1, 1988
Psychiatric and neurological manifestations in systemic lupus erythematosusL Lim, M A Ron, I E Ormerod, et al.QJM : Monthly Journal of the Association of Physicians|March 1, 1995
Management of mitochondrial disease on an intensive care unitR S Howard, S Russell, N Losseff, et al.Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 1993
Linkage analysis with chromosome 9 markers in hereditary essential tremorD Conway, P G Bain, T T Warner, et al.Brain : a Journal of Neurology|June 1, 1993
Linkage analysis in British and French families with idiopathic torsion dystoniaT T Warner, N A Fletcher, M B Davis, et al.Brain : a Journal of Neurology|August 1, 1992
Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutationA E Harding, M G Sweeney, D H Miller, et al.Experimental Neurology|May 1, 1991
Insertions in the prion protein gene in atypical dementiasF Owen, M Poulter, J Collinge, et al.Annals of Neurology|August 1, 1991
Presynaptic and postsynaptic striatal dopaminergic function in neuroacanthocytosis: a positron emission tomographic studyD J Brooks, V Ibanez, E D Playford, et al.Brain : a Journal of Neurology|December 1, 1995
Persistent functional deficit in multiple sclerosis and autosomal dominant cerebellar ataxia is associated with axon lossC A Davie, G J Barker, S Webb, et al.Nature Genetics|December 1, 1992
Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophyA R La Spada, D B Roling, A E Harding, et al.Journal of the Neurological Sciences|January 1, 1992
Evidence for intramitochondrial complementation between deleted and normal mitochondrial DNA in some patients with mitochondrial myopathyS R Hammans, M G Sweeney, I J Holt, et al.Pageof 21