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Archives of Neurology|May 1, 1997
Clinical characteristics of a chromosome 17-linked rapidly progressive familial frontotemporal dementiaH Basun, O Almkvist, K Axelman, et al.Human Mutation|March 25, 1999
Pathogenic presenilin 1 mutations (P436S & I143F) in early-onset Alzheimer's disease in the UK. Mutations in brief no. 223. OnlineM S Palmer, J A Beck, T A Campbell, et al.The New England Journal of Medicine|December 21, 1989
Oncogenic point mutations in the human retinoblastoma gene: their application to genetic counselingD W Yandell, T A Campbell, S H Dayton, et al.Journal of Neurochemistry|February 4, 1999
Quantification of axonal damage in traumatic brain injury: affinity purification and characterization of cerebrospinal fluid tau proteinsF P Zemlan, W S Rosenberg, P A Luebbe, et al.Magnetic Resonance Imaging|January 22, 1998
Imaging perfusion deficits in ischemic heart disease with susceptibility-enhanced T2-weighted MRI: preliminary human studiesG M Beache, S F Kulke, H L Kantor, et al.Human Genetics|September 1, 1996
Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP geneO Windl, M Dempster, J P Estibeiro, et al.Archives of Neurology|June 19, 2001
Autopsy-confirmed familial early-onset Alzheimer disease caused by the l153V presenilin 1 mutationJ C Janssen, P L Lantos, N C Fox, et al.Neurology|August 22, 2007
Inherited prion disease with 5-OPRI: phenotype modification by repeat length and codon 129S Mead, T E F Webb, T A Campbell, et al.Pageof 4