Wood NW - Search Results

1

Evaluation of four candidate genes encoding proteins of the dopamine pathway in familial and sporadic Parkinson's disease: evidence for association of a DRD2 allele.

Planté-Bordeneuve V, Taussig D, Thomas F, Said G, Wood NW, Marsden CD, Harding AE. Planté-Bordeneuve V, et al. Among authors: wood nw. Neurology. 1997 Jun;48(6):1589-93. doi: 10.1212/wnl.48.6.1589. Neurology. 1997. PMID: 9191771

2

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.

3

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

4

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

5

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

6

The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: genetic and physical mapping of the SCA7 locus.

David G, Giunti P, Abbas N, Coullin P, Stevanin G, Horta W, Gemmill R, Weissenbach J, Wood N, Cunha S, Drabkin H, Harding AE, Agid Y, Brice A. David G, et al. Am J Hum Genet. 1996 Dec;59(6):1328-36. Am J Hum Genet. 1996. PMID: 8940279 Free PMC article.

7

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

8

GTP cyclohydrolase I mutations in patients with dystonia responsive to anticholinergic drugs.

Jarman PR, Bandmann O, Marsden CD, Wood NW. Jarman PR, et al. Among authors: wood nw. J Neurol Neurosurg Psychiatry. 1997 Sep;63(3):304-8. doi: 10.1136/jnnp.63.3.304. J Neurol Neurosurg Psychiatry. 1997. PMID: 9328244 Free PMC article.

9

Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson's disease.

Bandmann O, Vaughan J, Holmans P, Marsden CD, Wood NW. Bandmann O, et al. Among authors: wood nw. Lancet. 1997 Oct 18;350(9085):1136-9. doi: 10.1016/s0140-6736(97)03495-8. Lancet. 1997. PMID: 9343502

10

Hereditary geniospasm: linkage to chromosome 9q13-q21 and evidence for genetic heterogeneity.

Jarman PR, Wood NW, Davis MT, Davis PV, Bhatia KP, Marsden CD, Davis MB. Jarman PR, et al. Among authors: wood nw. Am J Hum Genet. 1997 Oct;61(4):928-33. doi: 10.1086/514883. Am J Hum Genet. 1997. PMID: 9382105 Free PMC article.

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