Wood NW - Search Results

1

The alpha-synuclein gene in multiple system atrophy.

Ozawa T, Healy DG, Abou-Sleiman PM, Ahmadi KR, Quinn N, Lees AJ, Shaw K, Wullner U, Berciano J, Moller JC, Kamm C, Burk K, Josephs KA, Barone P, Tolosa E, Goldstein DB, Wenning G, Geser F, Holton JL, Gasser T, Revesz T, Wood NW; European MSA study group. Ozawa T, et al. Among authors: wood nw. J Neurol Neurosurg Psychiatry. 2006 Apr;77(4):464-7. doi: 10.1136/jnnp.2005.073528. J Neurol Neurosurg Psychiatry. 2006. PMID: 16543523 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

The T-cell receptor beta locus and susceptibility to multiple sclerosis.

Wood NW, Sawcer SJ, Kellar-Wood HF, Holmans P, Clayton D, Robertson N, Compston DA. Wood NW, et al. Neurology. 1995 Oct;45(10):1859-63. doi: 10.1212/wnl.45.10.1859. Neurology. 1995. PMID: 7477982

4

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.

5

No linkage between multiple sclerosis and the T cell receptor alpha chain locus.

Eoli M, Wood NW, Kellar-Wood HF, Holmans P, Clayton D, Compston DA. Eoli M, et al. Among authors: wood nw. J Neurol Sci. 1994 Jun;124(1):32-7. doi: 10.1016/0022-510x(94)90007-8. J Neurol Sci. 1994. PMID: 7931419

6

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

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

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.

9

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

10

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

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