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Studies in Health Technology and Informatics|August 22, 2015
Development of the SORRI-BAURU Posterior WalkerAnthony R J Nicholl, Renato G Busnardo, Luciana M da Silva, 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.
Acta Anaesthesiologica Belgica|May 12, 2000
"Recommendations for uniform reporting of data following major trauma--the Utstein style" (as of July 17, 1999). An International Trauma Anaesthesia and Critical Care Society (ITACCS)W F Dick, P J Baskett, C Grande, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 8, 2012
Systematic review and UK-based study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's diseaseLaura L Kilarski, Justin P Pearson, Victoria Newsway, 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.
Molecular Psychiatry|August 24, 2016
De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and femalesE E Palmer, T Stuhlmann, S Weinert, et al.
The Lancet. Neurology|June 12, 2018
LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing studyMarialuisa Quadri, Wim Mandemakers, Martyna M Grochowska, et al.
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