Showing results (461-470 of 571) with videos related to

Sort By:
Pageof 58
JAMA Neurology|April 26, 2016
Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial DiseaseMika H Martikainen, Yi Shiau Ng, Gráinne S Gorman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 22, 2016
Serum immune markers and disease progression in an incident Parkinson's disease cohort (ICICLE-PD)Caroline H Williams-Gray, Ruwani Wijeyekoon, Alison J Yarnall, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 20, 2017
Cerebral glucose metabolism and cognition in newly diagnosed Parkinson's disease: ICICLE-PD studyM J Firbank, A J Yarnall, R A Lawson, et al.
Journal of Medical Genetics|May 16, 2002
An MLH1 haplotype is over-represented on chromosomes carrying an HNPCC predisposing mutation in MLH1P Hutter, J Wijnen, C Rey-Berthod, et al.
Lancet (London, England)|October 7, 1997
New variant Creutzfeldt-Jakob disease: neurological features and diagnostic testsM Zeidler, G E Stewart, C R Barraclough, et al.
Human Genetics|July 4, 2006
A maternal hypomethylation syndrome presenting as transient neonatal diabetes mellitusD J G Mackay, S E Boonen, J Clayton-Smith, et al.
Plos Medicine|November 2, 2006
Atypical haemolytic uraemic syndrome associated with a hybrid complement geneJulian P Venables, Lisa Strain, Danny Routledge, et al.
Pageof 58