Wood NW - Search Results

1

Primary torsion dystonia: the search for genes is not over.

Jarman PR, del Grosso N, Valente EM, Leube B, Cassetta E, Bentivoglio AR, Waddy HM, Uitti RJ, Maraganore DM, Albanese A, Frontali M, Auburger G, Bressman SB, Wood NW, Nygaard TG. Jarman PR, et al. Among authors: wood nw. J Neurol Neurosurg Psychiatry. 1999 Sep;67(3):395-7. doi: 10.1136/jnnp.67.3.395. J Neurol Neurosurg Psychiatry. 1999. PMID: 10449567 Free PMC article.

2

Multiple sclerosis in the Cambridge health district of east Anglia.

Mumford CJ, Fraser MB, Wood NW, Compston DA. Mumford CJ, et al. Among authors: wood nw. J Neurol Neurosurg Psychiatry. 1992 Oct;55(10):877-82. doi: 10.1136/jnnp.55.10.877. J Neurol Neurosurg Psychiatry. 1992. PMID: 1431950 Free PMC article.

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

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

5

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

6

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

7

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.

8

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

9

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.

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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