Wood NW - Search Results

1

Large-scale pathways-based association study in amyotrophic lateral sclerosis.

Kasperaviciute D, Weale ME, Shianna KV, Banks GT, Simpson CL, Hansen VK, Turner MR, Shaw CE, Al-Chalabi A, Pall HS, Goodall EF, Morrison KE, Orrell RW, Beck M, Jablonka S, Sendtner M, Brockington A, Ince PG, Hartley J, Nixon H, Shaw PJ, Schiavo G, Wood NW, Goldstein DB, Fisher EM. Kasperaviciute D, et al. Among authors: wood nw. Brain. 2007 Sep;130(Pt 9):2292-301. doi: 10.1093/brain/awm055. Epub 2007 Apr 17. Brain. 2007. PMID: 17439985 Free article.

2

Susceptibility to multiple sclerosis and the immunoglobulin heavy chain variable region.

Wood NW, Sawcer SJ, Kellar-Wood HF, Holmans P, Clayton D, Robertson N, Compston DA. Wood NW, et al. J Neurol. 1995 Oct;242(10):677-82. doi: 10.1007/BF00866919. J Neurol. 1995. PMID: 8568530

3

Mitochondrial DNA polymorphisms in pathologically proven Parkinson's disease.

Bandmann O, Sweeney MG, Daniel SE, Marsden CD, Wood NW. Bandmann O, et al. Among authors: wood nw. J Neurol. 1997 Apr;244(4):262-5. doi: 10.1007/s004150050082. J Neurol. 1997. PMID: 9112596

4

Identification and sizing of the GAA trinucleotide repeat expansion of Friedreich's ataxia in 56 patients. Clinical and genetic correlates.

Lamont PJ, Davis MB, Wood NW. Lamont PJ, et al. Among authors: wood nw. Brain. 1997 Apr;120 ( Pt 4):673-80. doi: 10.1093/brain/120.4.673. Brain. 1997. PMID: 9153129

5

Multiple-system atrophy is genetically distinct from identified inherited causes of spinocerebellar degeneration.

Bandmann O, Sweeney MG, Daniel SE, Wenning GK, Quinn N, Marsden CD, Wood NW. Bandmann O, et al. Among authors: wood nw. Neurology. 1997 Dec;49(6):1598-604. doi: 10.1212/wnl.49.6.1598. Neurology. 1997. PMID: 9409353

6

Paroxysmal dystonic choreoathetosis. Genetic linkage studies in a British family.

Jarman PR, Davis MB, Hodgson SV, Marsden CD, Wood NW. Jarman PR, et al. Among authors: wood nw. Brain. 1997 Dec;120 ( Pt 12):2125-30. doi: 10.1093/brain/120.12.2125. Brain. 1997. PMID: 9448567

7

The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlates.

Giunti P, Sabbadini G, Sweeney MG, Davis MB, Veneziano L, Mantuano E, Federico A, Plasmati R, Frontali M, Wood NW. Giunti P, et al. Among authors: wood nw. Brain. 1998 Mar;121 ( Pt 3):459-67. doi: 10.1093/brain/121.3.459. Brain. 1998. PMID: 9549522

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: wood nw. Brain. 1998 Dec;121 ( Pt 12):2335-9. doi: 10.1093/brain/121.12.2335. Brain. 1998. PMID: 9874484

9

Mutations in the gene encoding human persyn are not associated with amyotrophic lateral sclerosis or familial Parkinson's disease.

Flowers JM, Leigh PN, Davies AM, Ninkina NN, Buchman VL, Vaughan J, Wood NW, Powell JF. Flowers JM, et al. Among authors: wood nw. Neurosci Lett. 1999 Oct 15;274(1):21-4. doi: 10.1016/s0304-3940(99)00673-4. Neurosci Lett. 1999. PMID: 10530510

10

The genetics of Parkinson's disease.

Spacey SD, Wood NW. Spacey SD, et al. Among authors: wood nw. Curr Opin Neurol. 1999 Aug;12(4):427-32. doi: 10.1097/00019052-199908000-00009. Curr Opin Neurol. 1999. PMID: 10555831 Review.

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