Wood NW - Search Results

1

Genotype-phenotype correlations, dystonia and disease progression in spinocerebellar ataxia type 14.

Chelban V, Wiethoff S, Fabian-Jessing BK, Haridy NA, Khan A, Efthymiou S, Becker EBE, O'Connor E, Hersheson J, Newland K, Hojland AT, Gregersen PA, Lindquist SG, Petersen MB, Nielsen JE, Nielsen M, Wood NW, Giunti P, Houlden H. Chelban V, et al. Among authors: wood nw. Mov Disord. 2018 Jul;33(7):1119-1129. doi: 10.1002/mds.27334. Epub 2018 Mar 30. Mov Disord. 2018. PMID: 29603387 Free PMC article.

2

Genetic aspects of Parkinson's disease.

Bandmann O, Marsden CD, Wood NW. Bandmann O, et al. Among authors: wood nw. Mov Disord. 1998 Mar;13(2):203-11. doi: 10.1002/mds.870130203. Mov Disord. 1998. PMID: 9539331 Review. No abstract available.

3

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

4

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

5

De novo expansion of intermediate alleles in spinocerebellar ataxia 7.

Stevanin G, Giunti P, Belal GD, Dürr A, Ruberg M, Wood N, Brice A. Stevanin G, et al. Hum Mol Genet. 1998 Oct;7(11):1809-13. doi: 10.1093/hmg/7.11.1809. Hum Mol Genet. 1998. PMID: 9736784

6

Molecular and clinical study of 18 families with ADCA type II: evidence for genetic heterogeneity and de novo mutation.

Giunti P, Stevanin G, Worth PF, David G, Brice A, Wood NW. Giunti P, et al. Among authors: wood nw. Am J Hum Genet. 1999 Jun;64(6):1594-603. doi: 10.1086/302406. Am J Hum Genet. 1999. PMID: 10330346 Free PMC article.

7

Autosomal dominant cerebellar ataxia type III: linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3.

Worth PF, Giunti P, Gardner-Thorpe C, Dixon PH, Davis MB, Wood NW. Worth PF, et al. Among authors: wood nw. Am J Hum Genet. 1999 Aug;65(2):420-6. doi: 10.1086/302495. Am J Hum Genet. 1999. PMID: 10417284 Free PMC article.

8

Neurofibrillary tangle parkinsonian disorders--tau pathology and tau genetics.

Morris HR, Lees AJ, Wood NW. Morris HR, et al. Among authors: wood nw. Mov Disord. 1999 Sep;14(5):731-6. doi: 10.1002/1531-8257(199909)14:5<731::aid-mds1004>3.0.co;2-j. Mov Disord. 1999. PMID: 10495033 Review.

9

Detailed genotyping demonstrates association between the slow acetylator genotype for N-acetyltransferase 2 (NAT2) and familial Parkinson's disease.

Bandmann O, Vaughan JR, Holmans P, Marsden CD, Wood NW. Bandmann O, et al. Among authors: wood nw. Mov Disord. 2000 Jan;15(1):30-5. doi: 10.1002/1531-8257(200001)15:1<30::aid-mds1007>3.0.co;2-v. Mov Disord. 2000. PMID: 10634239

10

Large, expanded repeats in SCA8 are not confined to patients with cerebellar ataxia.

Worth PF, Houlden H, Giunti P, Davis MB, Wood NW. Worth PF, et al. Among authors: wood nw. Nat Genet. 2000 Mar;24(3):214-5. doi: 10.1038/73411. Nat Genet. 2000. PMID: 10700168 No abstract available.

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