Wood N - Search Results

1

Phenotypic homogeneity of the Huntington disease-like presentation in a SCA17 family.

Schneider SA, van de Warrenburg BP, Hughes TD, Davis M, Sweeney M, Wood N, Quinn NP, Bhatia KP. Schneider SA, et al. Among authors: wood n. Neurology. 2006 Nov 14;67(9):1701-3. doi: 10.1212/01.wnl.0000242740.01273.00. Neurology. 2006. PMID: 17101913

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

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

5

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

6

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.

7

In vivo skeletal muscle mitochondrial function in Leber's hereditary optic neuropathy assessed by 31P magnetic resonance spectroscopy.

Lodi R, Taylor DJ, Tabrizi SJ, Kumar S, Sweeney M, Wood NW, Styles P, Radda GK, Schapira AH. Lodi R, et al. Among authors: wood nw. Ann Neurol. 1997 Oct;42(4):573-9. doi: 10.1002/ana.410420407. Ann Neurol. 1997. PMID: 9382468

8

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

9

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

10

Generalized chorea in two patients harboring the Friedreich's ataxia gene trinucleotide repeat expansion.

Hanna MG, Davis MB, Sweeney MG, Noursadeghi M, Ellis CJ, Elliot P, Wood NW, Marsden CD. Hanna MG, et al. Among authors: wood nw. Mov Disord. 1998 Mar;13(2):339-40. doi: 10.1002/mds.870130223. Mov Disord. 1998. PMID: 9539351

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