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Brain : a Journal of Neurology|June 1, 1993
Dementia associated with a 216 base pair insertion in the prion protein gene. Clinical and neuropathological featuresL W Duchen, M Poulter, A E HardingMuscle & Nerve. Supplement|January 1, 1995
Mitochondrial DNA diseases: genotype and phenotype in Leber's hereditary optic neuropathyA E Harding, P Riordan-Eva, G G GovanJournal of Medical Genetics|December 1, 1989
Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathyI J Holt, D H Miller, A E HardingRevue Neurologique|January 1, 1992
[Demonstration of genetic mutation in most of the amyloid neuropathies with sporadic occurrence]D Adams, M Reilly, A E Harding, et al.Journal of Medical Genetics|March 1, 1990
Pontobulbar palsy and neurosensory deafness (Brown-Vialetto-Van Laere syndrome) with possible autosomal dominant inheritanceS A Hawkins, N C Nevin, A E HardingBrain : a Journal of Neurology|June 1, 1994
Autosomal dominant cerebellar ataxia with pigmentary macular dystrophy. A clinical and genetic study of eight familiesT P Enevoldson, M D Sanders, A E HardingPostgraduate Medical Journal|April 1, 1986
Acute polyradiculoneuropathy complicating systemic lupus erythematosusS H Morgan, R P Kennett, C Dudley, et al.Brain : a Journal of Neurology|April 1, 1990
A genetic study of idiopathic torsion dystonia in the United KingdomN A Fletcher, A E Harding, C D MarsdenJournal of Neurology, Neurosurgery, and Psychiatry|February 1, 1996
Autosomal dominant optic atrophy with asymptomatic peripheral neuropathyR M Chalmers, A C Bird, A E HardingJournal of Neurology, Neurosurgery, and Psychiatry|August 1, 1984
Autosomal recessive late onset multisystem disorder with cerebellar cortical atrophy at necropsy: report of a familyA E Harding, J V Diengdoh, A J LeesPageof 21