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Annals of Neurology|November 1, 1982
Spinocerebellar degeneration secondary to chronic intestinal malabsorption: a vitamin E deficiency syndromeA E Harding, D P Muller, P K Thomas, et al.Brain : a Journal of Neurology|April 29, 1998
Influence of vision on upper limb reaching movements in patients with cerebellar ataxiaB L Day, P D Thompson, A E Harding, et al.Brain : a Journal of Neurology|June 1, 1995
Striatal D1 and D2 receptor binding in patients with Huntington's disease and other choreas. A PET studyN Turjanski, R Weeks, R Dolan, et al.Neurology|December 1, 1996
Anticipation in familial Parkinson's disease: a reanalysis of 13 United Kingdom kindredsD M Maraganore, D J Schaid, W A Rocca, 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.American Journal of Human Genetics|July 1, 1995
Pedigree analysis in Leber hereditary optic neuropathy families with a pathogenic mtDNA mutationA E Harding, M G Sweeney, G G Govan, et al.Archives of Neurology|October 1, 1990
Progressive myoclonic ataxia (the Ramsay Hunt syndrome)C D Marsden, A E Harding, J A Obeso, et al.British Journal of Rheumatology|November 1, 1984
Sjögren's syndrome presenting as a severe sensory neuropathy including involvement of the trigeminal nerveR G Hull, S H Morgan, A E Harding, et al.Annals of Neurology|March 1, 1991
A genetic study of idiopathic focal dystoniasH M Waddy, N A Fletcher, A E Harding, et al.Archives of Disease in Childhood|November 1, 1994
Mitochondrial DNA 8993 (NARP) mutation presenting with a heterogeneous phenotype including 'cerebral palsy'A Fryer, R Appleton, M G Sweeney, et al.Pageof 21