Warner T - Search Results

1

Silver syndrome is not linked to any of the previously established autosomal dominant hereditary spastic paraplegia loci.

Patel H, Hart PE, Warner T, Allen I, Phillimore HE, Silver JR, Wood NW, Jeffery S, Patton MA, Crosby AH. Patel H, et al. Among authors: warner t. Am J Med Genet. 2001 Jul 22;102(1):68-72. doi: 10.1002/1096-8628(20010722)102:1<68::aid-ajmg1411>3.0.co;2-r. Am J Med Genet. 2001. PMID: 11471175

2

The role of DYT1 in primary torsion dystonia in Europe.

Valente EM, Warner TT, Jarman PR, Mathen D, Fletcher NA, Marsden CD, Bhatia KP, Wood NW. Valente EM, et al. Among authors: warner tt. Brain. 1998 Dec;121 ( Pt 12):2335-9. doi: 10.1093/brain/121.12.2335. Brain. 1998. PMID: 9874484

3

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 mutations.

Valente EM, Povey S, Warner TT, Wood NW, Davis MB. Valente EM, et al. Among authors: warner tt. Ann Hum Genet. 1999 Jan;63(Pt 1):1-8. doi: 10.1046/j.1469-1809.1999.6310001.x. Ann Hum Genet. 1999. PMID: 10738516

4

Abnormal in vivo skeletal muscle energy metabolism in Huntington's disease and dentatorubropallidoluysian atrophy.

Lodi R, Schapira AH, Manners D, Styles P, Wood NW, Taylor DJ, Warner TT. Lodi R, et al. Among authors: warner tt. Ann Neurol. 2000 Jul;48(1):72-6. Ann Neurol. 2000. PMID: 10894218

5

The Silver syndrome variant of hereditary spastic paraplegia maps to chromosome 11q12-q14, with evidence for genetic heterogeneity within this subtype.

Patel H, Hart PE, Warner TT, Houlston RS, Patton MA, Jeffery S, Crosby AH. Patel H, et al. Among authors: warner tt. Am J Hum Genet. 2001 Jul;69(1):209-15. doi: 10.1086/321267. Epub 2001 May 25. Am J Hum Genet. 2001. PMID: 11389484 Free PMC article.

6

Cervical dystonia is associated with a polymorphism in the dopamine (D5) receptor gene.

Placzek MR, Misbahuddin A, Chaudhuri KR, Wood NW, Bhatia KP, Warner TT. Placzek MR, et al. Among authors: warner tt. J Neurol Neurosurg Psychiatry. 2001 Aug;71(2):262-4. doi: 10.1136/jnnp.71.2.262. J Neurol Neurosurg Psychiatry. 2001. PMID: 11459908 Free PMC article.

7

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 members.

Mead SH, Proukakis C, Wood N, Crosby AH, Plant GT, Warner TT. Mead SH, et al. Among authors: warner tt. J Neurol Neurosurg Psychiatry. 2001 Dec;71(6):788-91. doi: 10.1136/jnnp.71.6.788. J Neurol Neurosurg Psychiatry. 2001. PMID: 11723204 Free PMC article.

8

A polymorphism in the dopamine receptor DRD5 is associated with blepharospasm.

Misbahuddin A, Placzek MR, Chaudhuri KR, Wood NW, Bhatia KP, Warner TT. Misbahuddin A, et al. Among authors: warner tt. Neurology. 2002 Jan 8;58(1):124-6. doi: 10.1212/wnl.58.1.124. Neurology. 2002. PMID: 11781417

9

Three novel spastin (SPG4) mutations in families with autosomal dominant hereditary spastic paraplegia.

Proukakis C, Hart PE, Cornish A, Warner TT, Crosby AH. Proukakis C, et al. Among authors: warner tt. J Neurol Sci. 2002 Sep 15;201(1-2):65-9. doi: 10.1016/s0022-510x(02)00192-2. J Neurol Sci. 2002. PMID: 12163196

10

Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: evidence for a third EKD gene.

Spacey SD, Valente EM, Wali GM, Warner TT, Jarman PR, Schapira AH, Dixon PH, Davis MB, Bhatia KP, Wood NW. Spacey SD, et al. Among authors: warner tt. Mov Disord. 2002 Jul;17(4):717-25. doi: 10.1002/mds.10126. Mov Disord. 2002. PMID: 12210861

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