Wood NW - Search Results

1

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

2

The T-cell receptor beta locus and susceptibility to multiple sclerosis.

Wood NW, Sawcer SJ, Kellar-Wood HF, Holmans P, Clayton D, Robertson N, Compston DA. Wood NW, et al. Neurology. 1995 Oct;45(10):1859-63. doi: 10.1212/wnl.45.10.1859. Neurology. 1995. PMID: 7477982

3

No linkage or association between multiple sclerosis and the myelin basic protein gene in affected sibling pairs.

Wood NW, Holmans P, Clayton D, Robertson N, Compston DA. Wood NW, et al. J Neurol Neurosurg Psychiatry. 1994 Oct;57(10):1191-4. doi: 10.1136/jnnp.57.10.1191. J Neurol Neurosurg Psychiatry. 1994. PMID: 7523603 Free PMC article.

4

The British Isles survey of multiple sclerosis in twins.

Mumford CJ, Wood NW, Kellar-Wood H, Thorpe JW, Miller DH, Compston DA. Mumford CJ, et al. Among authors: wood nw. Neurology. 1994 Jan;44(1):11-5. doi: 10.1212/wnl.44.1.11. Neurology. 1994. PMID: 8290043

5

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

6

Evidence against an X-linked visual loss susceptibility locus in Leber hereditary optic neuropathy.

Chalmers RM, Davis MB, Sweeney MG, Wood NW, Harding AE. Chalmers RM, et al. Among authors: wood nw. Am J Hum Genet. 1996 Jul;59(1):103-8. Am J Hum Genet. 1996. PMID: 8659512 Free PMC article.

7

The human homologue of the weaver mouse gene in familial and sporadic Parkinson's disease.

Bandmann O, Davis MB, Marsden CD, Wood NW. Bandmann O, et al. Among authors: wood nw. Neuroscience. 1996 Jun;72(4):877-9. doi: 10.1016/0306-4522(96)00091-7. Neuroscience. 1996. PMID: 8735215

8

Dopa-responsive dystonia in British patients: new mutations of the GTP-cyclohydrolase I gene and evidence for genetic heterogeneity.

Bandmann O, Nygaard TG, Surtees R, Marsden CD, Wood NW, Harding AE. Bandmann O, et al. Among authors: wood nw. Hum Mol Genet. 1996 Mar;5(3):403-6. doi: 10.1093/hmg/5.3.403. Hum Mol Genet. 1996. PMID: 8852666

9

The GTP-cyclohydrolase I gene in atypical parkinsonian patients: a clinico-genetic study.

Bandmann O, Daniel S, Marsden CD, Wood NW, Harding AE. Bandmann O, et al. Among authors: wood nw. J Neurol Sci. 1996 Sep 15;141(1-2):27-32. doi: 10.1016/0022-510x(96)00098-6. J Neurol Sci. 1996. PMID: 8880688

10

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

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