Harding, A. E.

The clinical features of mitochondrial myopathy

PETTY, R. K. H., HARDING, A. E., & MORGAN-HUGHES, J. A. (1986) · Brain

Mitochondrial Function and PathologyMetabolism and Genetic Disorders

Cited by 417

A study of hereditary essential tremor

Bain, P. G., Findley, L. J., Thompson, P. D., Gresty, M. A., Rothwell, J. C., Harding, A. E., & Marsden, C. D. (1994) · Brain

Deep Brain Stimulation and Movement DisordersNeurological and metabolic disorders

Cited by 392

Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy.

Holt, I. J., Miller, D. H., & Harding, A. E. (1989) · Journal of Medical Genetics

Mitochondrial Function and PathologyHereditary Neurological Disorders

Cited by 159

Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis

Kellar‐Wood, H., Robertson, N., Govan, G. G., Compston, D. A. S., & Harding, A. E. (1994) · Annals of Neurology

Multiple Sclerosis Research StudiesMitochondrial Function and Pathology

Cited by 145