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

Por Chalmers, R M, Riordan-Eva, P, Wood, N W
Publicado em 1997

Introduction: genetic variation and human health

Por Stumpf, M.P.H, Goldstein, D.B, Wood, N.W
Publicado em 2005

Genetic association studies of complex neurological diseases

Por Abou‐Sleiman, P M, Hanna, M G, Wood, N W
Publicado em 2006

No linkage or association between multiple sclerosis and the myelin basic protein gene in affected sibling pairs.

Por Wood, N W, Holmans, P, Clayton, D, Robertson, N, Compston, D A
Publicado em 1994

Multiple sclerosis in the Cambridge health district of east Anglia.

Por Mumford, C J, Fraser, M B, Wood, N W, Compston, D A
Publicado em 1992

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

Por Giunti, P, Stevanin, G, Worth, P F, David, G, Brice, A, Wood, N W
Publicado em 1999

Evidence against an X-linked visual loss susceptibility locus in Leber hereditary optic neuropathy.

Por Chalmers, R. M., Davis, M. B., Sweeney, M. G., Wood, N. W., Harding, A. E.
Publicado em 1996

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

Por Worth, P F, Giunti, P, Gardner-Thorpe, C, Dixon, P H, Davis, M B, Wood, N W
Publicado em 1999

Screening of mutations in NOL3 in a myoclonic syndromes series

Por Macerollo, A., Mencacci, N. E., Erro, R., Cordivari, C., Edwards, M. J., Wood, N. W., Bhatia, Kailash P.
Publicado em 2014

Population genetic approaches to neurological disease: Parkinson's disease as an example

Por Gandhi, S, Abou-Sleiman, P.M, Healy, D.G, Weale, M, Gilks, W, Ahmadi, K, Goldstein, D.B, Wood, N.W
Publicado em 2005

Hereditary geniospasm: linkage to chromosome 9q13-q21 and evidence for genetic heterogeneity.

Por Jarman, P R, Wood, N W, Davis, M T, Davis, P V, Bhatia, K P, Marsden, C D, Davis, M B
Publicado em 1997

Expression of BRI2 mRNA and protein in normal human brain and familial British dementia: its relevance to the pathogenesis of disease

Por Lashley, T., Revesz, T., Plant, G., Bandopadhyay, R., Lees, A. J., Frangione, B., Wood, N. W., de Silva, R., Ghiso, J., Rostagno, A., Holton, J. L.
Publicado em 2008

GLUCOCEREBROSIDASE MUTATIONS IN 108 NEUROPATHOLOGICALLY CONFIRMED CASES OF MULTIPLE SYSTEM ATROPHY

Por Segarane, B, Li, A, Paudel, R, Scholz, S, Neumann, J, Lees, A, Revesz, T, Hardy, J, Mathias, C J., Wood, N W., Holton, J, Houlden, H
Publicado em 2009

Phosphorylation of HtrA2 by cyclin-dependent kinase-5 is important for mitochondrial function

Por Fitzgerald, J C, Camprubi, M D, Dunn, L, Wu, H-C, Ip, N Y, Kruger, R, Martins, L M, Wood, N W, Plun-Favreau, H
Publicado em 2012

Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA.

Por Hanna, M G, Nelson, I P, Rahman, S, Lane, R J, Land, J, Heales, S, Cooper, M J, Schapira, A H, Morgan-Hughes, J A, Wood, N W
Publicado em 1998

HtrA2 deficiency causes mitochondrial uncoupling through the F(1)F(0)-ATP synthase and consequent ATP depletion

Por Plun-Favreau, H, Burchell, V S, Holmström, K M, Yao, Z, Deas, E, Cain, K, Fedele, V, Moisoi, N, Campanella, M, Miguel Martins, L, Wood, N W, Gourine, A V, Abramov, A Y
Publicado em 2012

The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populations

Por Sharma, M, Mueller, J C, Zimprich, A, Lichtner, P, Hofer, A, Leitner, P, Maass, S, Berg, D, Dürr, A, Bonifati, V, De Michele, G, Oostra, B, Brice, A, Wood, N W, Muller‐Myhsok, B, Gasser, T
Publicado em 2006

An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathy.

Por Clark, K M, Taylor, R W, Johnson, M A, Chinnery, P F, Chrzanowska-Lightowlers, Z M, Andrews, R M, Nelson, I P, Wood, N W, Lamont, P J, Hanna, M G, Lightowlers, R N, Turnbull, D M
Publicado em 1999

Characterisation of a novel NR4A2 mutation in Parkinson’s disease brain

Por Sleiman, P.M.A., Healy, D.G., Muqit, M.M.K., Yang, Y.X., Van Der Brug, M., Holton, J.L., Revesz, T., Quinn, N.P., Bhatia, K., Diss, J.K.J., Lees, A.J., Cookson, M.R., Latchman, D.S., Wood, N.W.
Publicado no Neurosci Lett (2009)

Second consensus statement on the diagnosis of multiple system atrophy

Por Gilman, S, Wenning, G K., Low, P A., Brooks, D J., Mathias, C J., Trojanowski, J Q., Wood, N W., Colosimo, C, Dürr, A, Fowler, C J., Kaufmann, H, Klockgether, T, Lees, A, Poewe, W, Quinn, N, Revesz, T, Robertson, D, Sandroni, P, Seppi, K, Vidailhet, M
Publicado em 2008