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D J Nicholl

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European Journal of Neurology|November 29, 2013
The HhaI polymorphism in the CYP2D6 gene is not associated with Parkinson's disease in a Caucasian populationD J Nicholl, P Bennett, D B Ramsden, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 20, 2004
White matter abnormalities on MRI in neuroacanthocytosisD J Nicholl, I Sutton, M T Dotti, et al.
Clinical Medicine (London, England)|September 10, 2011
The inpatient neurology consultation service: value and costM R Douglas, D Peake, S G Sturman, et al.
Acta Neurologica Scandinavica|May 1, 2001
Clinical diagnosis of multiple system atrophy: level of agreement between Quinn's criteria and the consensus conference guidelinesC Colosimo, N Vanacore, V Bonifati, et al.
Parkinsonism & Related Disorders|January 31, 2015
Novel GCH1 variant in Dopa-responsive dystonia and Parkinson's diseaseA J Lewthwaite, T D Lambert, E B Rolfe, et al.
Neurology|October 22, 1998
Direct genetic evidence for involvement of tau in progressive supranuclear palsy. European Study Group on Atypical Parkinsonism ConsortiumP Bennett, V Bonifati, U Bonuccelli, et al.
Neurology|October 26, 1999
A study of five candidate genes in Parkinson's disease and related neurodegenerative disorders. European Study Group on Atypical ParkinsonismD J Nicholl, P Bennett, L Hiller, et al.
Neuroscience Letters|October 26, 1999
The tau gene in progressive supranuclear palsy: exclusion of mutations in coding exons and exon 10 splice sites, and identification of a new intronic variant of the disease-associated H1 haplotype in Italian casesV Bonifati, M Joosse, D J Nicholl, et al.
Brain : a Journal of Neurology|February 9, 2002
Two large British kindreds with familial Parkinson's disease: a clinico-pathological and genetic studyD J Nicholl, J R Vaughan, N L Khan, et al.
Neurology|July 13, 2005
Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypesV Bonifati, C F Rohé, G J Breedveld, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
European Journal of Neurology|November 29, 2013
The HhaI polymorphism in the CYP2D6 gene is not associated with Parkinson's disease in a Caucasian populationD J Nicholl, P Bennett, D B Ramsden, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 20, 2004
White matter abnormalities on MRI in neuroacanthocytosisD J Nicholl, I Sutton, M T Dotti, et al.
Clinical Medicine (London, England)|September 10, 2011
The inpatient neurology consultation service: value and costM R Douglas, D Peake, S G Sturman, et al.
Acta Neurologica Scandinavica|May 1, 2001
Clinical diagnosis of multiple system atrophy: level of agreement between Quinn's criteria and the consensus conference guidelinesC Colosimo, N Vanacore, V Bonifati, et al.
Parkinsonism & Related Disorders|January 31, 2015
Novel GCH1 variant in Dopa-responsive dystonia and Parkinson's diseaseA J Lewthwaite, T D Lambert, E B Rolfe, et al.
Neurology|October 22, 1998
Direct genetic evidence for involvement of tau in progressive supranuclear palsy. European Study Group on Atypical Parkinsonism ConsortiumP Bennett, V Bonifati, U Bonuccelli, et al.
Neurology|October 26, 1999
A study of five candidate genes in Parkinson's disease and related neurodegenerative disorders. European Study Group on Atypical ParkinsonismD J Nicholl, P Bennett, L Hiller, et al.
Neuroscience Letters|October 26, 1999
The tau gene in progressive supranuclear palsy: exclusion of mutations in coding exons and exon 10 splice sites, and identification of a new intronic variant of the disease-associated H1 haplotype in Italian casesV Bonifati, M Joosse, D J Nicholl, et al.
Brain : a Journal of Neurology|February 9, 2002
Two large British kindreds with familial Parkinson's disease: a clinico-pathological and genetic studyD J Nicholl, J R Vaughan, N L Khan, et al.
Neurology|July 13, 2005
Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypesV Bonifati, C F Rohé, G J Breedveld, et al.
Pageof 2