Warner TT - Search Results

1

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

2

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

Warner TT, Fletcher NA, Davis MB, Ahmad F, Conway D, Feve A, Rondot P, Marsden CD, Harding AE. Warner TT, et al. Brain. 1993 Jun;116 ( Pt 3):739-44. doi: 10.1093/brain/116.3.739. Brain. 1993. PMID: 8513401

3

Complex I function in familial and sporadic dystonia.

Schapira AH, Warner T, Gash MT, Cleeter MW, Marinho CF, Cooper JM. Schapira AH, et al. Ann Neurol. 1997 Apr;41(4):556-9. doi: 10.1002/ana.410410421. Ann Neurol. 1997. PMID: 9124815

4

The genetics of Parkinson's disease and parkinsonian syndromes.

Bajaj NP, Shaw C, Warner T, RayChaudhuri K. Bajaj NP, et al. J Neurol. 1998 Oct;245(10):625-33. doi: 10.1007/s004150050258. J Neurol. 1998. PMID: 9776460 Review.

5

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

6

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

7

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

8

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.

9

Dystonia: an update on genetics and treatment.

Misbahuddin A, Warner TT. Misbahuddin A, et al. Among authors: warner tt. Curr Opin Neurol. 2001 Aug;14(4):471-5. doi: 10.1097/00019052-200108000-00007. Curr Opin Neurol. 2001. PMID: 11470963 Review.

10

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. 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

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