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

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

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

Progressive neuronal degeneration of childhood with liver disease (Alpers' disease) presenting in young adultsHARDING, B. N; ALSANJARI, N; SMITH, S. J. M et al.Journal of neurology, neurosurgery and psychiatry. 1995, Vol 58, Num 3, pp 320-325, issn 0022-3050Conference Paper

Nigral dopaminergic cell loss in vitamin E deficient ratsDEXTER, D. T; ISHANTHI NANAYAKKARA; GOSS-SAMPSON, M. A et al.Neuroreport (Oxford). 1994, Vol 5, Num 14, pp 1773-1776, issn 0959-4965Article

The neuropathological features of neuroacanthocytosisRINNE, J. O; DANIEL, S. E; SCARAVILLI, F et al.Movement disorders. 1994, Vol 9, Num 3, pp 297-304, issn 0885-3185Article

Cortical myoclonus in Huntington's diseaseTHOMPSON, P. D; BHATIA, K. P; HARDING, A. E et al.Movement disorders. 1994, Vol 9, Num 6, pp 633-641, issn 0885-3185Article

Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosisKELLAR-WOOD, H; ROBERTSON, N; GOVAN, G. G et al.Annals of neurology. 1994, Vol 36, Num 1, pp 109-112, issn 0364-5134Article

The mitochondrial DNA transfer RNA^Lys A→G⁽⁸³⁴⁴⁾ mutation and the syndrome of myoclonic epilepsy with ragged red fibres (MERRF) : relationship of clinical phenotype to proportion of mutant mitochondrial DNAHAMMANS, S. R; SWEENEY, M. G; BROCKINGTON, M et al.Brain. 1993, Vol 116, pp 617-632, issn 0006-8950, 3Article

Transthyretin gene mutations in British and French patients with amyloid neuropathyBHATIA, K; REILLY, M; ADAMS, D et al.Journal of neurology, neurosurgery and psychiatry. 1993, Vol 56, Num 6, pp 694-697, issn 0022-3050Conference Paper

Evidence for intramitochondrial complementation between deleted and normal mitochondrial DNA in some patients with mitochondrial myopathyHAMMANS, S. R; SWEENEY, M. G; HOLT, I. J et al.Journal of the neurological sciences. 1992, Vol 107, Num 1, pp 87-92, issn 0022-510XArticle

Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's diseaseSMITH, C. A. D; GOUGH, A. C; ROLAND WOLF, C et al.Lancet (British edition). 1992, Vol 339, Num 8806, pp 1375-1377, issn 0140-6736Article

Mitochondrial encephalopathies : molecular genetic diagnosis from blood samplesHAMMANS, S. R; SWEENEY, M. G; BROCKINGTON, M et al.Lancet (British edition). 1991, Vol 337, Num 8753, pp 1311-1313, issn 0140-6736Article