A. Harding

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Persistent functional deficit in multiple sclerosis and autosomal dominant cerebellar ataxia is associated with axon loss.

A. Thompson, G. Barker, D. Miller, 1995, Brain : a journal of neurology.

Influence of vision on upper limb reaching movements in patients with cerebellar ataxia.

B. Day, P. Thompson, C. Marsden, 1998, Brain : a journal of neurology.

The phenotypic manifestations of chromosome 17p11.2 duplication.

A. Harding, P. Thomas, W. Marques, 1997, Brain : a journal of neurology.

The relationship between striatal dopamine receptor binding and cognitive performance in Huntington's disease.

T. Robbins, D. Brooks, A. Lawrence, 1998, Brain : a journal of neurology.

The neuropathological features of neuroacanthocytosis

Marsden, C. Marsden, F. Scaravilli, 1994, Movement disorders : official journal of the Movement Disorder Society.

Spinocerebellar degeneration secondary to chronic intestinal malabsorption: A vitamin E deficiency syndrome

A. Harding, H. Willison, D. Muller, 1982, Annals of neurology.

Parkinson's disease in twins studied with 18F‐dopa and positron emission tomography

A. E. Harding, T. R. Zimmerman, D. J. Brooks, 1992, Neurology.

Apo E genotypes in multiple sclerosis, Parkinson's disease, schwannomas and late-onset Alzheimer's disease.

D. Rubinsztein, J. Xuereb, A. Harding, 1994, Molecular and cellular probes.

‘Idiopathic’ late onset cerebellar ataxia A clinical and genetic study of 36 cases

A. Harding, 1981, Journal of the Neurological Sciences.

Degenerative cerebellar ataxia and focal dystonia

C. Marsden, A. Harding, N. Fletcher, 1988, Movement disorders : official journal of the Movement Disorder Society.

Hereditary demyelinating neuropathy of infancy. A genetically complex syndrome.

F. Muntoni, A. Harding, R. King, 1997, Brain : a journal of neurology.

Vitamin E and the nervous system.

A. Harding, 1987, Critical reviews in neurobiology.

Neuroleptic malignant syndrome associated with metoclopramide.

N. Legg, A. Harding, M. B. Robinson, 1985, Journal of neurology, neurosurgery, and psychiatry.

Spinal and cutaneous schwannomatosis is a variant form of type 2 neurofibromatosis: a clinical and molecular study.

D. Evans, T. Strachan, S. Huson, 1997, Journal of neurology, neurosurgery, and psychiatry.

Genomic imprinting and anticipation in idiopathic torsion dystonia

A. Korczyn, D. Pauls, R. Inzelberg, 1993, Neurology.

Intrafamilial correlation in idiopathic torsion dystonia

C. Marsden, A. Harding, N. Fletcher, 1991, Movement disorders : official journal of the Movement Disorder Society.

Carpal tunnel syndrome related to antebrachial Cimino-Brescia fistula.

A. Harding, J. Le Fanu, 1977, Journal of neurology, neurosurgery, and psychiatry.

Prenatal diagnosis of mitochondrial DNA8993 T----G disease.

A. Harding, M. Davis, M. Sweeney, 1992, American journal of human genetics.

Progressive myoclonic ataxia (the Ramsay Hunt syndrome).

C. Marsden, J. Obeso, A. Harding, 1990, Archives of neurology.

Autosomal dominant late onset cerebellar ataxia with myoclonus, peripheral neuropathy and sensorineural deafness: a clinicopathological report.

F. Scaravilli, P. Rudge, A. Halliday, 1984, Journal of neurology, neurosurgery, and psychiatry.

Spinocerebellar degeneration associated with a selective defect of vitamin E absorption.

A. Harding, D. Muller, C. Ellis, 1985, The New England journal of medicine.

Linkage analysis in British and French families with idiopathic torsion dystonia.

C. Marsden, A. Harding, M. Davis, 1993, Brain : a journal of neurology.

MATTERS ARISING

A. Harding, P. Thomas, R. Hardie, 1991 .

Early onset cerebellar ataxia with retained tendon reflexes: a clinical and genetic study of a disorder distinct from Friedreich's ataxia.

A. Harding, 1981, Journal of neurology, neurosurgery, and psychiatry.

Hereditary distal spinal muscular atrophy A report on 34 cases and a review of the literature

A. Harding, P. Thomas, P. Thomas, 1980, Journal of the Neurological Sciences.

Arg296 to Cys296 polymorphism in exon 6 of cytochrome P-450-2D6 (CYP2D6) is not associated with multiple system atrophy.

N. Quinn, A. Harding, G. Wenning, 1995, Journal of neurology, neurosurgery, and psychiatry.

Evaluation of four candidate genes encoding proteins of the dopamine pathway in familial and sporadic Parkinson's disease

C D Marsden, N W Wood, C. Marsden, 1997, Neurology.

Sequence ofthesuperoxide dismutase 1(SOD1) gene infamilial Parkinson's disease

C. Marsden, A. Harding, M. Davis, 1995 .

Sequence of the superoxide dismutase 1 (SOD 1) gene in familial Parkinson's disease.

C. Marsden, A. Harding, M. Davis, 1995, Journal of neurology, neurosurgery, and psychiatry.

Inherited movement disorders.

A. Harding, 1994, Bailliere's clinical neurology.

Chronic asymmetrical spinal muscular atrophy

N. Murray, A. Harding, P. Bradbury, 1983, Journal of the Neurological Sciences.

disease . polymorphism in familial Parkinson ' s Debrisoquine hydroxylase gene

C. Marsden, A. Harding, M. Davis, 2022 .

PLASMA EXCHANGE AND IMMUNOSUPPRESSION IN THE STIFF MAN SYNDROME

C. Marsden, A. Harding, J. R. Batchelor, 1989, The Lancet.

A familial disorder associated with palatal myoclonus, other brainstem signs, tetraparesis, ataxia and Rosenthal fibre formation.

C. Marsden, R. Greenwood, F. Scaravilli, 1993, Journal of neurology, neurosurgery, and psychiatry.

Familial amyloid polyneuropathy (TTR ala 60) in north west Ireland: a clinical, genetic, and epidemiological study.

H. Staunton, A. Harding, M. Reilly, 1995, Journal of neurology, neurosurgery, and psychiatry.

The diverse neurological features of Niemann‐Pick disease type C: A report of two cases

E. Brett, A. Harding, B. Lake, 1988, Movement disorders : official journal of the Movement Disorder Society.

Pontine myelinolysis presenting with acute parkinsonism as a sequel of corrected hyponatraemia.

A. Kermode, A. Harding, P. Anand, 1990, Journal of neurology, neurosurgery, and psychiatry.

Disorders of the motor neuron

A. Harding, K. Morrison, 1994 .

Disorders of the motor neurone.

A. Harding, K. Morrison, 1994, Bailliere's clinical neurology.

From the syndrome of Charcot, Marie and Tooth to disorders of peripheral myelin proteins.

A. Harding, 1995, Brain : a journal of neurology.

Deletions of chromosome 17p11.2 in multifocal neuropathies

A. Harding, J. Tyson, S. Malcolm, 1996, Annals of neurology.

Peroneal muscular atrophy with pyramidal features.

A. Harding, P. Thomas, 1984, Journal of neurology, neurosurgery, and psychiatry.

Progressive neuronal degeneration of childhood with liver disease (Alpers' disease) presenting in young adults.

S. Smith, B. Harding, F. Scaravilli, 1995 .

Transthyretin gene analysis in European patients with suspected familial amyloid polyneuropathy

D. Booth, A. Harding, P. Thomas, 1996, Neuromuscular Disorders.

Presymptomatic detection or exclusion of prion protein gene defects in families with inherited prion diseases.

T. Crow, J. Collinge, A. Harding, 1991, American journal of human genetics.

Contrast-enhanced lesions on computerised tomography in multiple sclerosis.

A. Whiteley, E. Radue, A. Harding, 1978, Journal of neurology, neurosurgery, and psychiatry.

Familial cerebral amyloid angiopathy with nonneuritic amyloid plaque formation.

G. Plant, T. Révész, R. Barnard, 1990, Brain : a journal of neurology.

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)--confirmation by cerebral biopsy in 2 cases.

M. Rossor, F. Scaravilli, A. Harding, 1995, Clinical neuropathology.

A study of the relationship between neurological function and serum vitamin E concentrations in patients with cystic fibrosis.

A. Kriss, A. Harding, H. Willison, 1985, Journal of neurology, neurosurgery, and psychiatry.

Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation.

W. Mcdonald, A. Harding, D. Compston, 1992, Brain : a journal of neurology.

Intracerebral haemorrhage complicating dural arteriovenous fistula: a report of two cases.

M. Johnson, B. Kendall, A. Harding, 1984, Journal of neurology, neurosurgery, and psychiatry.

The sensory neuropathy of Friedreich's ataxia: an autopsy study of a case with prolonged survival

A. Harding, R. King, J. Muddle, 2004, Acta Neuropathologica.

Hereditary spastic paraplegias.

A. Harding, 1993, Seminars in neurology.

Haplotype analysis of French, British and other European patients with familial amyloid polyneuropathy (met 30 and tyr 77)

A. Harding, M. Davis, M. Reilly, 1995, Journal of Neurology.

Transthyretin gene analysis in European patients with suspected familial amyloid polyneuropathy.

D. Booth, A. Harding, P. Thomas, 1995 .

Erratum: Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease (The Lancet, vol. 339/8806 (1375-1377))

P. Leigh, A. Schapira, A. Harding, 1992 .

Diaphragmatic weakness in hereditary motor and sensory neuropathy.

A. Harding, P. Thomas, R. Hardie, 1990, Journal of neurology, neurosurgery, and psychiatry.

Serum vitamin E concentrations in degenerative ataxias.

A. Harding, D. Muller, C. Macevilly, 1989, Journal of neurology, neurosurgery, and psychiatry.

Degenerative ataxic disorders: still perplexing.

A. Harding, 1987, British medical journal.

Serum vitamin E concentrations are normal in Friedreich's ataxia.

A. Harding, D. Muller, S. Matthews, 1987, Journal of neurology, neurosurgery, and psychiatry.

CLASSIFICATION OF THE HEREDITARY ATAXIAS AND PARAPLEGIAS

A. Harding, 1983, The Lancet.

MOLECULAR GENETICS OF AMYLOID NEUROPATHY IN EUROPE

A. Harding, P. Thomas, R. King, 1989, The Lancet.

Mutation analysis in patients with possible but apparently sporadic Huntington's disease

C. Marsden, N. Quinn, A. Harding, 1994, The Lancet.

A follow‐up study of isolated cases of suspected Huntington's disease

C. Marsden, F. Scaravilli, A. Harding, 1992, Annals of neurology.

Neuroacanthocytosis. A clinical, haematological and pathological study of 19 cases.

J S Owen, V. P. Misra, A. Harding, 1991, Brain : a journal of neurology.

The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'.

A. Harding, 1982, Brain : a journal of neurology.

X-linked recessive bulbospinal neuronopathy: a report of ten cases.

A. Harding, P. Thomas, M. Baraitser, 1982, Journal of neurology, neurosurgery, and psychiatry.

Clinical and molecular neurogenetics in neurosurgery.

A. Harding, 1993, Advances and technical standards in neurosurgery.

Transthyretin gene mutations in British and French patients with amyloid neuropathy.

K. Bhatia, A. Harding, P. Thomas, 1993, Journal of neurology, neurosurgery, and psychiatry.

French patients with amyloid neuropathy . Transthyretin gene mutations in British and

A. Harding, P. Thomas, M. Davis, 2022 .

Age at onset in Huntington's disease and methylation at D4S95.

W. Reik, A. Harding, E. Maher, 1993, Journal of medical genetics.

The clinical features of hereditary motor and sensory neuropathy types I and II.

P K Thomas, A. Harding, P. Thomas, 1980, Brain : a journal of neurology.

The gene for Huntington's disease.

A. Harding, 1993, BMJ.

Inherited Neuronal Atrophy and Degeneration Predominantly of Lower Motor Neurons

A. Harding, 2005 .

Discordance for late-onset degenerative ataxia in monozygous triplets

A. Harding, T. Sura, A. Boughey, 1991, Journal of Neurology.

Peripheral neuropathy in the Chediak-Higashi syndrome

V. P. Misra, A. Harding, R. King, 2004, Acta Neuropathologica.

A novel point mutation in the mcleod syndrome gene in neuroacanthocytosis

A. Monaco, A. Harding, A. Harding, 1996, Annals of neurology.

Acanthocytosis, Retinitis Pigmentosa, and Pallidal Degeneration

A. E. Harding, J. S. Owen, C. Marsden, 1995, Neurology.

Nigral degeneration in neuroacanthocytosis

C D Marsden, F Scaravilli, J O Rinne, 1994, Neurology.

An adult onset hexosaminidase A deficiency syndrome with sensory neuropathy and internuclear ophthalmoplegia.

V. P. Misra, A. Harding, P. Thomas, 1991, Journal of neurology, neurosurgery, and psychiatry.

Adult onset supranuclear ophthalmoplegia, cerebellar ataxia, and neurogenic proximal muscle weakness in a brother and sister: another hexosaminidase A deficiency syndrome.

A. Harding, E. Young, F. Schon, 1987, Journal of neurology, neurosurgery, and psychiatry.

Presynaptic and postsynaptic striatal dopaminergic function in neuroacanthocytosis: A positron emission tomographic study

V. Ibáñez, G. Sawle, D. Brooks, 1991, Annals of neurology.

Friedreich's ataxia: a clinical and genetic study of 90 families with an analysis of early diagnostic criteria and intrafamilial clustering of clinical features.

A. Harding, 1981, Brain : a journal of neurology.

Degenerative ataxic disorders

A. Harding, 1986, Trends in Neurosciences.

Molecular genetics of peripheral neuropathies.

A. Harding, 1995, Bailliere's clinical neurology.

Autosomal recessive forms of hereditary motor and sensory neuropathy.

P K Thomas, A. Harding, P. Thomas, 1980, Journal of neurology, neurosurgery, and psychiatry.

Hereditary "pure" spastic paraplegia: a clinical and genetic study of 22 families.

A. Harding, 1981, Journal of neurology, neurosurgery, and psychiatry.

Movement disorders in mitochondrial myopathies. A study of nine cases with two autopsy studies

C. Marsden, S. Smith, F. Scaravilli, 1990, Movement disorders : official journal of the Movement Disorder Society.

Autosomal dominant cerebellar ataxia with pigmentary macular dystrophy. A clinical and genetic study of eight families.

M. Sanders, A. Harding, T. Enevoldson, 1994, Brain : a journal of neurology.

Central nervous system haemangioblastoma: a clinical and genetic study of 52 cases.

A. Harding, N. Fletcher, A. Boughey, 1990, Journal of neurology, neurosurgery, and psychiatry.

Genetic aspects of hereditary motor and sensory neuropathy (types I and II)

A. Harding, A. Harding, P. Thomas, 1980, Journal of medical genetics.

Clinical features and classification of inherited ataxias.

A. Harding, 1993, Advances in neurology.

Peripheral neuropathy associated with the sicca syndrome.

A. Harding, R. Kennett, 1986, Journal of neurology, neurosurgery, and psychiatry.

Sjögren's syndrome presenting as a severe sensory neuropathy including involvement of the trigeminal nerve.

G. Hughes, A. Harding, S. Morgan, 1984, British journal of rheumatology.

Cerebellar and spinocerebellar disorders

Nw Wood, Ae Harding, N. Wood, 2000 .

Striatal D1 and D2 receptor binding in patients with Huntington's disease and other choreas. A PET study.

D. Brooks, R. Dolan, D. Brooks, 1995, Brain : a journal of neurology.

Ataxia telangiectasia: A reappraisal of the ocular motor features and their value in the diagnosis of atypical cases

G. Plant, A. Bronstein, A. Harding, 1989, Movement disorders : official journal of the Movement Disorder Society.

Dementia associated with a 216 base pair insertion in the prion protein gene. Clinical and neuropathological features.

A. Harding, L. Duchen, M. Poulter, 1993, Brain : a journal of neurology.

Regeneration following tibial nerve crush in the rabbit: the effect of proximal constriction.

A. Harding, K. Reiners, R. Gilliatt, 1987, Journal of neurology, neurosurgery, and psychiatry.

A study of hereditary essential tremor.

C D Marsden, P. Thompson, C. Marsden, 1994, Brain : a journal of neurology.

The hereditary ataxias and related disorders

A. Harding, 1984 .

Inherited Neuropathies: The Interface between Molecular Genetics and Pathology

A. Harding, P. Thomas, 1993, Brain pathology.

Pupillary light-near dissociation in paraproteinaemic neuropathy: A case report

A. Harding, R. Williams, 1985 .

Demyelination following diphtheria toxin in the presence of axonal atrophy

A. Harding, M. Baba, K. Reiners, 1984, Journal of the Neurological Sciences.

A clinical and genetic study of familial Parkinson's disease

C. Marsden, D. Maraganore, A. Harding, 1991, Movement disorders : official journal of the Movement Disorder Society.

Hereditary motor and sensory neuropathies and hereditary spastic paraplegia: A magnetic stimulation study

N. Murray, A. Harding, P. Thomas, 1990, Annals of neurology.

Intracranial hypertension following psittacosis.

A. Harding, M. Prevett, 1993, Journal of neurology, neurosurgery, and psychiatry.

AN INVESTIGATION INTO THE CAUSE OF ARTHRITIC MUSCULAR ATROPHY.

A. Harding, 1929 .

Debrisoquine hydroxylase gene polymorphism in familial Parkinson's disease.

C. Marsden, A. Harding, M. Davis, 1994, Journal of neurology, neurosurgery, and psychiatry.

A genetic study of idiopathic focal dystonias

C. Marsden, A. Harding, N. Fletcher, 1991, Annals of neurology.

Type 1 Arnold-Chiari malformation in a 77 year old woman.

P. Trend, A. Harding, D. M. Halpin, 1990, Journal of neurology, neurosurgery, and psychiatry.

Tyrosine hydroxylase and levodopa responsive dystonia.

C. Marsden, J. Mallet, A. Harding, 1989, Journal of neurology, neurosurgery, and psychiatry.

Exclusion of the DYT1 locus in familial torticollis

N. Risch, D. Maraganore, L. Almasy, 1996, Annals of neurology.

A case‐control study of idiopathic torsion dystonia

C. Marsden, A. Harding, N. Fletcher, 1991, Movement disorders : official journal of the Movement Disorder Society.

A genetic study of idiopathic torsion dystonia in the United Kingdom.

C. Marsden, A. Harding, N. Fletcher, 1990, Brain : a journal of neurology.

EEG and evoked potential findings in mitochondrial myopathies

S. Smith, A. Harding, 1993, Journal of Neurology.

Arthritic muscular atrophy: The oxygen consumption of atrophied muscles

A. Harding, 1926 .

Magnetic resonance imaging in degenerative ataxic disorders.

G Johnson, E P du Boulay, D. MacManus, 1994, Journal of neurology, neurosurgery, and psychiatry.

[Demonstration of genetic mutation in most of the amyloid neuropathies with sporadic occurrence].

A. Harding, M. Reilly, D. Adams, 1992, Revue neurologique.

A dementing illness associated with a novel insertion in the prion protein gene.

T. Crow, J. Collinge, A. Harding, 1992, Brain research. Molecular brain research.

X-linked recessivebulbospinal neuronopathy: areportoftencases

A. Harding, P. Thomas, M. Baraitser, 1982 .

Striatal D1 and D2 dopamine receptor loss in asymptomatic mutation carriers of Huntington's disease

D. Brooks, D. Brooks, P. Piccini, 1996, Annals of neurology.

The relationship between trauma and idiopathic torsion dystonia.

C. Marsden, A. Harding, N. Fletcher, 1991, Journal of neurology, neurosurgery, and psychiatry.

Coexistence of hereditary motor and sensory neuropathy type IA and IGM paraproteinemic neuropathy

A. Harding, R. King, S. Malcolm, 1993, Annals of neurology.

Cerebellar presentation of multiple system atrophy

C. Mathias, N. Quinn, E. Kraft, 1997, Movement disorders : official journal of the Movement Disorder Society.

A CLINICAL AND MOLECULAR-GENETIC STUDY OF DENTATORUBROPALLIDOLUYSIAN ATROPHY IN 4 EUROPEAN FAMILIES

M. Honavar, T. Warner, A. Harding, 1995 .

Leukocyte glutamate dehydrogenase activity in patients with degenerative neurological disorders.

C. Marsden, N. Quinn, A. Harding, 1988, Journal of neurology, neurosurgery, and psychiatry.

Autosomal recessive late onset multisystem disorder with cerebellar cortical atrophy at necropsy: report of a family.

A. Lees, A. Harding, J. Diengdoh, 1984, Journal of neurology, neurosurgery, and psychiatry.

Cortical control of movement in Huntington's disease. A PET activation study.

D. Brooks, D. Brooks, P. Piccini, 1997, Brain : a journal of neurology.

Central motor conduction in degenerative ataxic disorders: a magnetic stimulation study.

K. Mills, D. Claus, N. Murray, 1988, Journal of neurology, neurosurgery, and psychiatry.

proximal constriction . crush in the rabbit : the effect of Regeneration following tibial nerve

A. Harding, K. Reiners, R. Gilliatt, 2022 .

Inherited prion disease (PrP lysine 200) in Britain: two case reports.

J Collinge, M. Palmer, J. Collinge, 1993, BMJ.

Predictive testing for Huntington's disease: after the gene. The United Kingdom Huntington's Disease Prediction Consortium.

A. Harding, S. Simpson, 1993, Journal of medical genetics.

Encephalomyeloneuropathy in the absence of a detectable neoplasm

S. Love, F. Scaravilli, S. Daniel, 1985, Acta Neuropathologica.

A study of the effects of isaxonine on vincristine-induced peripheral neuropathy in man and regeneration following peripheral nerve crush in the rat.

A. Harding, C. Fowler, P. Le Quesne, 1985, Journal of Neurology Neurosurgery & Psychiatry.

Botulinum toxin treatment in spasmodic torticollis.

A J Lees, A. Lees, Francesco Barbieri, 1990, Journal of neurology, neurosurgery, and psychiatry.

The role of NMR imaging in the assessment of multiple sclerosis and isolated neurological lesions. A quantitative study.

B E Kendall, G Johnson, P S Tofts, 1987, Brain : a journal of neurology.

Distal and scapuloperoneal distributions of muscle involvement occurring within a family with type I hereditary motor and sensory neuropathy

A. Harding, P. Thomas, 2004, Journal of Neurology.

Improvement in the POEMS syndrome after administration of tamoxifen.

A. Harding, T. Enevoldson, 1992, Journal of neurology, neurosurgery, and psychiatry.

Progressive neuronal degeneration of childhood with liver disease (Alpers' disease) presenting in young adults.

S. Smith, B. Harding, F. Scaravilli, 1995, Journal of neurology, neurosurgery, and psychiatry.

Pontobulbar palsy and neurosensory deafness (Brown-Vialetto-Van Laere syndrome) with possible autosomal dominant inheritance.

A. Harding, A. Harding, N. Nevin, 1990, Journal of medical genetics.

Associative learning in patients with cerebellar ataxia.

N P Quinn, R. Passingham, M. Rushworth, 1996, Behavioral neuroscience.

Irish (Donegal) amyloidosis is associated with the transthyretinALA60 (Appalachian) variant.

H. Staunton, A. Harding, M. Davis, 1991, Brain : a journal of neurology.

FAMILIAL DEMENTIA IN RELATION TO THE 144 BP INSERT AND ITS IMPLICATIONS

Martin O. Leach, T. J. Crow, Mark Poulter, 1992 .