Warner TT - Search Results

1

A clinical, genetic and candidate gene study of Silver syndrome, a complicated form of hereditary spastic paraplegia.

Warner TT, Patel H, Proukakis C, Reed JA, McKie L, Wills A, Patton MA, Crosby AH. Warner TT, et al. J Neurol. 2004 Sep;251(9):1068-74. doi: 10.1007/s00415-004-0401-8. J Neurol. 2004. PMID: 15372247

2

A clinical and molecular genetic study of dentatorubropallidoluysian atrophy in four European families.

Warner TT, Williams LD, Walker RW, Flinter F, Robb SA, Bundey SE, Honavar M, Harding AE. Warner TT, et al. Ann Neurol. 1995 Apr;37(4):452-9. doi: 10.1002/ana.410370407. Ann Neurol. 1995. PMID: 7717681

3

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

4

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

5

Genetic counselling in mitochondrial diseases.

Warner TT, Schapira AH. Warner TT, et al. Curr Opin Neurol. 1997 Oct;10(5):408-12. doi: 10.1097/00019052-199710000-00009. Curr Opin Neurol. 1997. PMID: 9330887 Review.

6

The role of the alpha-synuclein gene mutation in patients with sporadic Parkinson's disease in the United Kingdom.

Warner TT, Schapira AH. Warner TT, et al. J Neurol Neurosurg Psychiatry. 1998 Sep;65(3):378-9. doi: 10.1136/jnnp.65.3.378. J Neurol Neurosurg Psychiatry. 1998. PMID: 9728955 Free PMC article.

7

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.

8

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

9

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.

10

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.

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