Wood NW - Search Results

1

Dejerine-Sottas neuropathy and PMP22 point mutations: a new base pair substitution and a possible "hot spot" on Ser72.

Marques W Jr, Thomas PK, Sweeney MG, Carr L, Wood NW. Marques W Jr, et al. Among authors: wood nw. Ann Neurol. 1998 May;43(5):680-3. doi: 10.1002/ana.410430521. Ann Neurol. 1998. PMID: 9585367

2

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

3

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.

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

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.

6

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

7

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

8

Effects of intravenous methylprednisolone on outcome in MRI-based prognostic subgroups in acute optic neuritis.

Kapoor R, Miller DH, Jones SJ, Plant GT, Brusa A, Gass A, Hawkins CP, Page R, Wood NW, Compston DA, Moseley IF, McDonald WI. Kapoor R, et al. Among authors: wood nw. Neurology. 1998 Jan;50(1):230-7. doi: 10.1212/wnl.50.1.230. Neurology. 1998. PMID: 9443485 Clinical Trial.

9

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

10

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

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