Showing results (61-70 of 208) with videos related to
Sort By:
Pageof 21
Nucleic Acids Research|June 26, 1989
Deletions of muscle mitochondrial DNA in mitochondrial myopathies: sequence analysis and possible mechanismsI J Holt, A E Harding, J A Morgan-HughesAnnals of Neurology|February 1, 1996
Deletions of chromosome 17p11.2 in multifocal neuropathiesJ Tyson, S Malcolm, P K Thomas, et al.Journal of the Neurological Sciences|May 1, 1984
Demyelination following diphtheria toxin in the presence of axonal atrophyM Baba, R W Gilliatt, A E Harding, et al.Annals of Neurology|August 1, 1996
Sequence of mitochondrial DNA in patients with multiple sclerosisR M Chalmers, N Robertson, DAS Compston, et al.Brain : a Journal of Neurology|October 1, 1986
The clinical features of mitochondrial myopathyR K Petty, A E Harding, J A Morgan-HughesNature|February 25, 1988
Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathiesI J Holt, A E Harding, J A Morgan-HughesJournal of Medical Genetics|March 1, 1992
Distal spinal muscular atrophy with vocal cord paralysisC Pridmore, M Baraitser, E M Brett, et al.Journal of Neurology, Neurosurgery, and Psychiatry|September 1, 1985
A study of the effects of isaxonine on vincristine-induced peripheral neuropathy in man and regeneration following peripheral nerve crush in the ratP M Le Quesne, C J Fowler, A E HardingActa Neuropathologica|January 1, 1985
Encephalomyeloneuropathy in the absence of a detectable neoplasm. Clinical and postmortem findings in three casesS E Daniel, S Love, F Scaravilli, et al.Human Genetics|May 1, 1988
Mitochondrial DNA polymorphism in mitochondrial myopathyI J Holt, A E Harding, J A Morgan-HughesPageof 21