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Authors: A. E. HARDING
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Journal Article

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

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A D Lawrence and others
Brain, Volume 121, Issue 7, Jul 1998, Pages 1343–1355, https://doi.org/10.1093/brain/121.7.1343
Published: 01 July 1998
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Influence of vision on upper limb reaching movements in patients with cerebellar ataxia. Get access

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B L Day and others
Brain, Volume 121, Issue 2, Feb 1998, Pages 357–372, https://doi.org/10.1093/brain/121.2.357
Published: 01 February 1998
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Cortical control of movement in Huntington's disease. A PET activation study. Get access

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R A Weeks and others
Brain, Volume 120, Issue 9, Sep 1997, Pages 1569–1578, https://doi.org/10.1093/brain/120.9.1569
Published: 01 September 1997
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The phenotypic manifestations of chromosome 17p11.2 duplication. Get access

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P K Thomas and others
Brain, Volume 120, Issue 3, Mar 1997, Pages 465–478, https://doi.org/10.1093/brain/120.3.465
Published: 01 March 1997
Journal Article

Hereditary demyelinating neuropathy of infancy. A genetically complex syndrome. Get access

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J Tyson and others
Brain, Volume 120, Issue 1, Jan 1997, Pages 47–63, https://doi.org/10.1093/brain/120.1.47
Published: 01 January 1997
Journal Article

A case-control study of Leber's hereditary optic neuropathy Get access

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R. M. Chalmers and A. E. Harding
Brain, Volume 119, Issue 5, October 1996, Pages 1481–1486, https://doi.org/10.1093/brain/119.5.1481
Published: 01 October 1996
Journal Article

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

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C. A. Davie and others
Brain, Volume 119, Issue 4, August 1996, Page 1415, https://doi.org/10.1093/brain/119.4.1415
Published: 01 August 1996
Journal Article

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

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C. A. Davie and others
Brain, Volume 118, Issue 6, December 1995, Pages 1583–1592, https://doi.org/10.1093/brain/118.6.1583
Published: 01 December 1995
Journal Article

Detection of the Machado-Joseph disease/spinocerebellar ataxia three trinucleotide repeat expansion in families with autosomal dominant motor disorders, including the Drew family of Walworth Get access

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P. Giunti and others
Brain, Volume 118, Issue 5, October 1995, Pages 1077–1085, https://doi.org/10.1093/brain/118.5.1077
Published: 01 October 1995
Journal Article

Transthyretin gene analysis in European patients with suspected familial amyloid polyneuropathy Get access

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M. M. Reilly and others
Brain, Volume 118, Issue 4, August 1995, Pages 849–856, https://doi.org/10.1093/brain/118.4.849
Published: 01 August 1995
Journal Article

The mitochondrial DNA transfer RNA Leu(UUR) A→G(3243) mutation: A clinical and genetic study Get access

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S. R. Hammans and others
Brain, Volume 118, Issue 3, June 1995, Pages 721–734, https://doi.org/10.1093/brain/118.3.721
Published: 01 June 1995
Journal Article

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

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A. E. Harding
Brain, Volume 118, Issue 3, June 1995, Pages 809–818, https://doi.org/10.1093/brain/118.3.809
Published: 01 June 1995
Journal Article

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

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N. Turjanski and others
Brain, Volume 118, Issue 3, June 1995, Pages 689–696, https://doi.org/10.1093/brain/118.3.689
Published: 01 June 1995
Journal Article

The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation Get access

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P. Riordan-Eva and others
Brain, Volume 118, Issue 2, April 1995, Pages 319–337, https://doi.org/10.1093/brain/118.2.319
Published: 01 April 1995
Journal Article

A study of hereditary essential tremor Get access

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P. G. Bain and others
Brain, Volume 117, Issue 4, August 1994, Pages 805–824, https://doi.org/10.1093/brain/117.4.805
Published: 01 August 1994
Journal Article

The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias Get access

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P. Giunti and others
Brain, Volume 117, Issue 4, August 1994, Pages 645–649, https://doi.org/10.1093/brain/117.4.645
Published: 01 August 1994
Journal Article

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

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T. P. Enevoldson and others
Brain, Volume 117, Issue 3, June 1994, Pages 445–460, https://doi.org/10.1093/brain/117.3.445
Published: 01 June 1994
Journal Article

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

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L. W. Duchen and others
Brain, Volume 116, Issue 3, June 1993, Pages 555–567, https://doi.org/10.1093/brain/116.3.555
Published: 01 June 1993
Journal Article

The mitochondrial DNA transfer RNALysA→G[8344] mutation and the syndrome of myoclonic epilepsy with ragged red fibres [MERRF]: Relationship of clinical phenotype to proporation of mutant mitochondrial DNA Get access

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S. R. Hammans and others
Brain, Volume 116, Issue 3, June 1993, Pages 617–632, https://doi.org/10.1093/brain/116.3.617
Published: 01 June 1993
Journal Article

Linkage analysis in British and French families with idiopathic torsion dystonia Get access

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T. T. Warner and others
Brain, Volume 116, Issue 3, June 1993, Pages 739–744, https://doi.org/10.1093/brain/116.3.739
Published: 01 June 1993