Showing results (101-110 of 112) with videos related to

Sort By:
Pageof 12
Proceedings of the National Academy of Sciences of the United States of America|March 5, 2014
Activating mutations in STIM1 and ORAI1 cause overlapping syndromes of tubular myopathy and congenital miosisVasyl Nesin, Graham Wiley, Maria Kousi, et al.
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.
Public Health|March 18, 2023
Did the UK's public health shielding policy protect the clinically extremely vulnerable during the COVID-19 pandemic in Wales? Results of EVITE Immunity, a linked data retrospective studyH Snooks, A Watkins, J Lyons, 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.
Pageof 12