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G G Lennox

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Bailliere'S Clinical Neurology|April 1, 1997

Dementia with Lewy bodiesG G Lennox, J S Lowe

Movement Disorders : Official Journal of the Movement Disorder Society|May 1, 1994

Autosomal-dominant dentatorubropallidoluysian atrophy in the United KingdomT T Warner, G G Lennox, I Janota, et al.

European Journal of Neurology|December 25, 2003

Rapidly reversible dementia in cerebral amyloid inflammatory vasculopathyK A C Harkness, A Coles, U Pohl, et al.

American Journal of Human Genetics|August 1, 1996

Mutations associated with variant phenotypes in ataxia-telangiectasiaC M McConville, T Stankovic, P J Byrd, et al.

Journal of Neurology, Neurosurgery, and Psychiatry|June 18, 2003

Differences in the diagnostic accuracy of acute stroke clinical subtypes defined by multimodal magnetic resonance imagingS J Allder, A R Moody, A L Martel, et al.

Brain : a Journal of Neurology|October 1, 1995

Progressive myoclonic ataxia associated with coeliac disease. The myoclonus is of cortical origin, but the pathology is in the cerebellumK P Bhatia, P Brown, R Gregory, et al.

Lancet (London, England)|November 7, 1999

Limitations of clinical diagnosis in acute strokeS J Allder, A R Moody, A L Martel, et al.

Brain : a Journal of Neurology|June 1, 1993

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 DNAS R Hammans, M G Sweeney, M Brockington, et al.

American Journal of Human Genetics|April 16, 1998

ATM mutations and phenotypes in ataxia-telangiectasia families in the British Isles: expression of mutant ATM and the risk of leukemia, lymphoma, and breast cancerT Stankovic, A M Kidd, A Sutcliffe, et al.

Archives of Neurology|May 21, 2003

Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraineE E Kors, J Haan, N J Giffin, et al.

Pageof 2

Search research articles

Showing results (1-10 of 11) with videos related to

Sort By:

Pageof 2

Bailliere'S Clinical Neurology|April 1, 1997

Dementia with Lewy bodiesG G Lennox, J S Lowe

Movement Disorders : Official Journal of the Movement Disorder Society|May 1, 1994

Autosomal-dominant dentatorubropallidoluysian atrophy in the United KingdomT T Warner, G G Lennox, I Janota, et al.

European Journal of Neurology|December 25, 2003

Rapidly reversible dementia in cerebral amyloid inflammatory vasculopathyK A C Harkness, A Coles, U Pohl, et al.

American Journal of Human Genetics|August 1, 1996

Mutations associated with variant phenotypes in ataxia-telangiectasiaC M McConville, T Stankovic, P J Byrd, et al.

Journal of Neurology, Neurosurgery, and Psychiatry|June 18, 2003

Differences in the diagnostic accuracy of acute stroke clinical subtypes defined by multimodal magnetic resonance imagingS J Allder, A R Moody, A L Martel, et al.

Brain : a Journal of Neurology|October 1, 1995

Progressive myoclonic ataxia associated with coeliac disease. The myoclonus is of cortical origin, but the pathology is in the cerebellumK P Bhatia, P Brown, R Gregory, et al.

Lancet (London, England)|November 7, 1999

Limitations of clinical diagnosis in acute strokeS J Allder, A R Moody, A L Martel, et al.

Brain : a Journal of Neurology|June 1, 1993

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 DNAS R Hammans, M G Sweeney, M Brockington, et al.

American Journal of Human Genetics|April 16, 1998

ATM mutations and phenotypes in ataxia-telangiectasia families in the British Isles: expression of mutant ATM and the risk of leukemia, lymphoma, and breast cancerT Stankovic, A M Kidd, A Sutcliffe, et al.

Archives of Neurology|May 21, 2003

Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraineE E Kors, J Haan, N J Giffin, et al.

Pageof 2