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Journal of Inherited Metabolic Disease|January 1, 1992
Deletions of the mitochondrial genomeA E Harding, S R HammansJournal of the Neurological Sciences|March 1, 1980
Hereditary distal spinal muscular atrophy. A report on 34 cases and a review of the literatureA E Harding, P K ThomasBritish Journal of Hospital Medicine|July 1, 1991
Mitochondrial disease and mitochondrial DNAS R Hammans, A E HardingBailliere'S Clinical Neurology|August 1, 1994
Disorders of the motor neuroneK E Morrison, A E HardingJournal of Neurology|January 1, 1980
Distal and scapuloperoneal distributions of muscle involvement occurring within a family with type I hereditary motor and sensory neuropathyA E Harding, P K ThomasJournal of Neurology, Neurosurgery, and Psychiatry|May 1, 1977
Carpal tunnel syndrome related to antebrachial Cimino-Brescia fistulaA E Harding, J Le FanuJournal of Neurology, Neurosurgery, and Psychiatry|February 1, 1984
Peroneal muscular atrophy with pyramidal featuresA E Harding, P K ThomasJournal of Medical Genetics|December 1, 1993
Predictive testing for Huntington's disease: after the gene. The United Kingdom Huntington's Disease Prediction ConsortiumS A Simpson, A E HardingBrain : a Journal of Neurology|June 1, 1980
The clinical features of hereditary motor and sensory neuropathy types I and IIA E Harding, P K ThomasPageof 21