Subdural haematoma in two patients with chronic neurological disordersHARDING, A. E.British medical journal (1857). 1984, Vol 288, Num 6435, pp 1986-1987, issn 0007-1447Article

From the syndrome of Charcot, Marie and Tooth to disorders of peripheral myelin proteinsHARDING, A. E.Brain. 1995, Vol 118, pp 809-818, issn 0006-8950, 3Article

Viewpoints on the Ramsay Hunt syndrome. III: Ramsay Hunt syndrome, Unverricht-Lundborg disease, or what?HARDING, A. E.Movement disorders. 1989, Vol 4, Num 1, pp 18-19, issn 0885-3185Article

Neurogenetics updateHARDING, A. E.Journal of the neurological sciences. 1994, Vol 126, Num 1, pp 90-93, issn 0022-510XArticle

Clinical and molecular neurogenetics in neurosurgeryHARDING, A. E.Advances and technical standards in neurosurgery. 1993, Vol 20, pp 81-104, issn 0095-4829Article

The DNA laboratory and neurological practiceHARDING, A. E.Journal of neurology, neurosurgery and psychiatry. 1993, Vol 56, Num 3, pp 229-233, issn 0022-3050Article

Clinical features and classification of inherited ataxiasHARDING, A. E.Advances in neurology. 1993, Vol 61, pp 1-14, issn 0091-3952Article

Genetic prediction in Huntington's disease: what are the limitations imposed by pedigree structure?MISRA, V. P; BARAITSER, M; HARDING, A. E et al.Movement disorders. 1988, Vol 3, Num 3, pp 233-236, issn 0885-3185Article

Dementia associated with a 216 base pair insertion in the prion protein gene : clinical and neuropathological featuresDUCHEN, L. W; POULTER, M; HARDING, A. E et al.Brain. 1993, Vol 116, pp 555-567, issn 0006-8950, 3Article

Mitochondrial myopathiesHARDING, A. E; HOLT, I. J.British medical bulletin. 1989, Vol 45, Num 3, pp 760-771, issn 0007-1420Article

Adult onset supranuclear ophthalmoplegia, cerebellar ataxia, and neurogenic proximal muscle weakness in a brother and sister: another hexosaminidase A deficiency syndromeHARDING, A. E; YOUNG, E. P; SCHON, F et al.Journal of neurology, neurosurgery and psychiatry. 1987, Vol 50, Num 6, pp 687-690, issn 0022-3050Article

Peripheral neuropathy associated with the sicca syndromeKENNETT, R. P; HARDING, A. E.Journal of neurology, neurosurgery and psychiatry. 1986, Vol 49, Num 1, pp 90-92, issn 0022-3050Article

Peroneal muscular atrophy with pyramidal featuresHARDING, A. E; THOMAS, P. K.Journal of neurology, neurosurgery and psychiatry. 1983, Vol 47, Num 2, pp 168-172, issn 0022-3050Article

Detection of the Machado-Joseph disease/spinocerebellar ataxia three trinucleotide repeat expansion in families with autosomal dominant motor disorders, including the Drew family of WalworthGIUNTI, P; SWEENEY, M. G; HARDING, A. E et al.Brain. 1995, Vol 118, pp 1077-1085, issn 0006-8950, 5Article

EEG and evoked potential findings in mitochondrial myopathiesSMITH, S. J. M; HARDING, A. E.Journal of neurology. 1993, Vol 240, Num 6, pp 367-372, issn 0340-5354Article

Predictive testing for Huntington's disease : after the geneSIMPSON, S. A; HARDING, A. E.Journal of medical genetics. 1993, Vol 30, Num 12, pp 1036-1038, issn 0022-2593Article

The relationship between striatal dopamine receptor binding and cognitive performance in Huntington's diseaseLAWRENCE, A. D; WEEKS, R. A; BROOKS, D. J et al.Brain. 1998, Vol 121, pp 1343-1355, issn 0006-8950, 7Article

¹¹C-diprenorphine binding in Huntington's disease : A comparison of region of interest analysis with statistical parametric mappingWEEKS, R. A; CUNNINGHAM, V. J; PICCINI, P et al.Journal of cerebral blood flow and metabolism. 1997, Vol 17, Num 9, pp 943-949, issn 0271-678XArticle

A novel point mutation in the McLeod syndrome gene in neuroacanthocytosisHO, M. F; CHALMERS, R. M; DAVIS, M. B et al.Annals of neurology. 1996, Vol 39, Num 5, pp 672-675, issn 0364-5134Article

Evidence against an X-linked visual loss susceptibility locus in leber hereditary optic neuropathyCHALMERS, R. M; DAVIS, M. B; SWEENEY, M. G et al.American journal of human genetics. 1996, Vol 59, Num 1, pp 103-108, issn 0002-9297Article

The GTP-cyclohydrolase I gene in atypical Parkinsonian patients : a clinico-genetic studyBANDMANN, O; DANIEL, S; MARSDEN, C. D et al.Journal of the neurological sciences. 1996, Vol 141, Num 1-2, pp 27-32, issn 0022-510XArticle

A new mitochondrial DNA mutation associated with progressive dementia and chorea : a clinical, pathological, and molecular genetic studyNELSON, I; HANNA, M. G; ALSANJARI, N et al.Annals of neurology. 1995, Vol 37, Num 3, pp 400-403, issn 0364-5134Article

Haplotype analysis of French, British and other European patients with familial amyloid polyneuropathy (met 30 and tyr 77)REILLY, M. M; ADAMS, M; DAVIS, M. B et al.Journal of neurology. 1995, Vol 242, Num 10, pp 664-668, issn 0340-5354Article

The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutationRIORDAN-EVA, P; SANDERS, M. D; GOVAN, G. G et al.Brain. 1995, Vol 118, pp 319-337, issn 0006-8950, 2Article

Persistent functional deficit in multiple sclerosis and autosomal dominant cerebellar ataxia is associated with axon lossDAVIE, C. A; BARKER, G. J; WEBB, S et al.Brain. 1995, Vol 118, pp 1583-1592, issn 0006-8950, 6Article