Wood NW - Search Results

1

Mutations in HPCA cause autosomal-recessive primary isolated dystonia.

Charlesworth G, Angelova PR, Bartolomé-Robledo F, Ryten M, Trabzuni D, Stamelou M, Abramov AY, Bhatia KP, Wood NW. Charlesworth G, et al. Among authors: wood nw. Am J Hum Genet. 2015 Apr 2;96(4):657-65. doi: 10.1016/j.ajhg.2015.02.007. Epub 2015 Mar 19. Am J Hum Genet. 2015. PMID: 25799108 Free PMC article.

2

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

3

Autosomal recessive inheritance of hereditary motor and sensory neuropathy with optic atrophy.

Chalmers RM, Riordan-Eva P, Wood NW. Chalmers RM, et al. Among authors: wood nw. J Neurol Neurosurg Psychiatry. 1997 Apr;62(4):385-7. doi: 10.1136/jnnp.62.4.385. J Neurol Neurosurg Psychiatry. 1997. PMID: 9120454 Free PMC article.

4

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.

5

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.

6

Sequencing of the alpha-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations. The European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD).

Vaughan JR, Farrer MJ, Wszolek ZK, Gasser T, Durr A, Agid Y, Bonifati V, DeMichele G, Volpe G, Lincoln S, Breteler M, Meco G, Brice A, Marsden CD, Hardy J, Wood NW. Vaughan JR, et al. Among authors: wood nw. Hum Mol Genet. 1998 Apr;7(4):751-3. doi: 10.1093/hmg/7.4.751. Hum Mol Genet. 1998. PMID: 9499430

7

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

8

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.

9

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.

10

A new family with paroxysmal exercise induced dystonia and migraine: a clinical and genetic study.

Münchau A, Valente EM, Shahidi GA, Eunson LH, Hanna MG, Quinn NP, Schapira AH, Wood NW, Bhatia KP. Münchau A, et al. Among authors: wood nw. J Neurol Neurosurg Psychiatry. 2000 May;68(5):609-14. doi: 10.1136/jnnp.68.5.609. J Neurol Neurosurg Psychiatry. 2000. PMID: 10766892 Free PMC article.

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