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T T Warner

Showing results (11-20 of 41) with videos related to

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The Journal of Infection|March 1, 1992
Reactivation of tuberculous lymphadenitis during pregnancyT T Warner, S H Khoo, E G Wilkins
Journal of Neurology, Neurosurgery, and Psychiatry|November 2, 2001
Friedreich's ataxia presenting as an isolated spastic paraparesisP A Wilkinson, J L Bradley, T T Warner
Rheumatology (Oxford, England)|January 4, 2001
Churg-Strauss syndrome presenting with visual lossJ Carmichael, M Conron, H Beynon, et al.
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.
Neuropathology and Applied Neurobiology|April 13, 2019
Review: Clinical, neuropathological and genetic features of Lewy body dementiasD Hansen, H Ling, T Lashley, et al.
Journal of the Neurological Sciences|November 11, 2003
SPG3A mutation screening in English families with early onset autosomal dominant hereditary spastic paraplegiaP A Wilkinson, P E Hart, H Patel, et al.
Annals of Human Genetics|March 30, 2000
Detailed haplotype analysis in Ashkenazi Jewish and non-Jewish British dystonic patients carrying the GAG deletion in the DYT1 gene: evidence for a limited number of founder mutationsE M Valente, S Povey, T T Warner, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 28, 2001
A large family with hereditary spastic paraparesis due to a frame shift mutation of the spastin (SPG4) gene: association with multiple sclerosis in two affected siblings and epilepsy in other affected family membersS H Mead, C Proukakis, N Wood, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 19, 2001
Cervical dystonia is associated with a polymorphism in the dopamine (D5) receptor geneM R Placzek, A Misbahuddin, K R Chaudhuri, et al.
Neurology|January 10, 2002
A polymorphism in the dopamine receptor DRD5 is associated with blepharospasmA Misbahuddin, M R Placzek, K R Chaudhuri, et al.
Pageof 5

Showing results (11-20 of 41) with videos related to

Sort By:
Pageof 5
The Journal of Infection|March 1, 1992
Reactivation of tuberculous lymphadenitis during pregnancyT T Warner, S H Khoo, E G Wilkins
Journal of Neurology, Neurosurgery, and Psychiatry|November 2, 2001
Friedreich's ataxia presenting as an isolated spastic paraparesisP A Wilkinson, J L Bradley, T T Warner
Rheumatology (Oxford, England)|January 4, 2001
Churg-Strauss syndrome presenting with visual lossJ Carmichael, M Conron, H Beynon, et al.
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.
Neuropathology and Applied Neurobiology|April 13, 2019
Review: Clinical, neuropathological and genetic features of Lewy body dementiasD Hansen, H Ling, T Lashley, et al.
Journal of the Neurological Sciences|November 11, 2003
SPG3A mutation screening in English families with early onset autosomal dominant hereditary spastic paraplegiaP A Wilkinson, P E Hart, H Patel, et al.
Annals of Human Genetics|March 30, 2000
Detailed haplotype analysis in Ashkenazi Jewish and non-Jewish British dystonic patients carrying the GAG deletion in the DYT1 gene: evidence for a limited number of founder mutationsE M Valente, S Povey, T T Warner, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 28, 2001
A large family with hereditary spastic paraparesis due to a frame shift mutation of the spastin (SPG4) gene: association with multiple sclerosis in two affected siblings and epilepsy in other affected family membersS H Mead, C Proukakis, N Wood, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 19, 2001
Cervical dystonia is associated with a polymorphism in the dopamine (D5) receptor geneM R Placzek, A Misbahuddin, K R Chaudhuri, et al.
Neurology|January 10, 2002
A polymorphism in the dopamine receptor DRD5 is associated with blepharospasmA Misbahuddin, M R Placzek, K R Chaudhuri, et al.
Pageof 5