N. Wood

发表

A polymorphism in the dopamine receptor DRD5 is associated with blepharospasm

K. Bhatia, K. Chaudhuri, A. Misbahuddin, 2002, Neurology.

Tendency towards being a “Morning person” increases risk of Parkinson’s disease: evidence from Mendelian randomisation

D. Hinds, J. Hardy, N. Wood, 2018, bioRxiv.

Genetic overlap between Alzheimer’s disease and Parkinson’s disease at the MAPT locus

A Smith, M A Pericak-Vance, L A Farrer, 2015, Molecular Psychiatry.

The genetic and pathological classification of familial frontotemporal dementia.

J. Hardy, P. Lantos, M. Rossor, 2001, Archives of neurology.

Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism

Y. Agid, A. Dürr, A. Brice, 1998, The Lancet.

Paroxysmal dystonic choreoathetosis. Genetic linkage studies in a British family.

C. Marsden, P. Jarman, N. Wood, 1997, Brain : a journal of neurology.

Second consensus statement on the diagnosis of multiple system atrophy

P Sandroni, P A Low, N Quinn, 2008, Neurology.

The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study Group.

M. T. Pellecchia, E. Tolosa, H. Wichmann, 2005, Brain : a journal of neurology.

Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype

M N Rossor, I Litvan, A J Lees, 2001, Neurology.

Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern India

K. Bhatia, N. Wood, M. Davis, 2004, Journal of Neurology, Neurosurgery & Psychiatry.

Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14.

N. Rahman, P. Futreal, N. Norton, 2001, American journal of human genetics.

GLUCOCEREBROSIDASE MUTATIONS IN 108 NEUROPATHOLOGICALLY CONFIRMED CASES OF MULTIPLE SYSTEM ATROPHY

Sonja W. Scholz, J. Hardy, A. Lees, 2009, Neurology.

Mutations in the HSP27 (HSPB1) gene cause dominant, recessive, and sporadic distal HMN/CMT type 2

N. Wood, N. Wood, F. W. Vrièze, 2008, Neurology.

Clinical heterogeneity and genotype‐phenotype correlations in hereditary spastic paraplegia because of Spatacsin mutations (SPG11)

N. Wood, H. Houlden, C. Paisán-Ruiz, 2008, European journal of neurology.

Familial cerebral amyloid angiopathy related to stroke and dementia.

J. Holton, T. Révész, N. Wood, 2001, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Linkage analysis on the SCA11 locus

Paola Giunti, Nw Wood, H Houlden, 2006 .

Chromosome 13 dementia syndromes as models of neurodegeneration

G. Plant, J. Holton, T. Révész, 2001, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Familial dopa-responsive cervical dystonia

S. Schneider, K. Bhatia, F. Asmus, 2006, Neurology.

Phenotypic homogeneity of the Huntington disease–like presentation in a SCA17 family

S A Schneider, B P C van de Warrenburg, T D Hughes, 2006, Neurology.

Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson's disease

C. Marsden, P. Holmans, N. Wood, 1997, The Lancet.

First of two parts

Finland., J. Finsterer, M. Rossor, 2001 .

EFNS task force on molecular diagnosis of neurologic disorders Guidelines for the molecular diagnosis of inherited neurologic diseases First of two parts

J. Finsterer, M. Rossor, M. Zeviani, 2001, European journal of neurology.

A clinical and genetic study of SPG5A linked autosomal recessive hereditary spastic paraplegia

A. Schapira, N. Wood, T. Warner, 2003, Neurology.

CCM1 gene mutations in families segregating cerebral cavernous malformations

J. Dichgans, G. Rouleau, A. Siegel, 2001, Neurology.

Hyposmia in G2019S LRRK2-related parkinsonism

J. Holton, A. Petrie, C. Sampaio, 2008, Neurology.

The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlates.

A. Federico, N. Wood, M. Davis, 1998, Brain : a journal of neurology.

Cerebellar and spinocerebellar disorders

Nw Wood, Ae Harding, N. Wood, 2000 .

Central nervous system involvement in a novel connexin 32 mutation affecting identical twins

N. Wood, W. Marques, M. Sweeney, 1999, Journal of neurology, neurosurgery, and psychiatry.

Regional distribution of amyloid-Bri deposition and its association with neurofibrillary degeneration in familial British dementia.

L. Martinian, T. Révész, J. Holton, 2001, The American journal of pathology.

Genetics of Parkinsonism: a review.

N. Wood, M. Davis, J. Vaughan, 2001, Annals of human genetics.

Pathological inclusion bodies in tauopathies contain distinct complements of tau with three or four microtubule‐binding repeat domains as demonstrated by new specific monoclonal antibodies

J. Holton, A. Lees, T. Révész, 2003, Neuropathology and applied neurobiology.

Mutations in the Novel Protein PRRT2 Cause Infantile Convulsions with Paroxysmal Kinesigenic Dyskinesia

Lynch, J. Jankovic, A. Bowcock, 2012 .

Identification and sizing of the GAA trinucleotide repeat expansion of Friedreich's ataxia in 56 patients. Clinical and genetic correlates.

N. Wood, N. Wood, M. Davis, 1997, Brain : a journal of neurology.

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

N. Wood, A. Harding, M. Davis, 1996, American journal of human genetics.

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

C. Marsden, P. Jarman, K. Bhatia, 1997, American journal of human genetics.

The European Multiple System Atrophy-Study Group (EMSA-SG)

F. Kopper, C. Colosimo, N. Schimke, 2005, Journal of Neural Transmission.

Strong association of the Saitohin gene Q7 variant with progressive supranuclear palsy

M. Weale, A. Lees, N. Wood, 2003, Neurology.

Thr(118)Met amino acid substitution in the peripheral myelin protein 22 does not influence the clinical phenotype of Charcot-Marie-Tooth disease type 1A due to the 17p11.2-p12 duplication.

N. Wood, W. Marques, W. Marques, 2003, Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas.

Multiple system atrophy/progressive supranuclear palsy: α-Synuclein, synphilin, tau, and APOE

P. Lantos, N. Cairns, D. Burn, 2000, Neurology.

connexin 32 mutation affecting identical twins Central nervous system involvement in a novel

N. Wood, M. Sweeney, M. Marques, 2022 .