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Brain : a Journal of Neurology|June 28, 2008
PET amyloid ligand [11C]PIB uptake shows predominantly striatal increase in variant Alzheimer's diseaseJ Koivunen, A Verkkoniemi, S Aalto, et al.Stroke|August 4, 2001
Phenotype of a homozygous CADASIL patient in comparison to 9 age-matched heterozygous patients with the same R133C Notch3 mutationS Tuominen, V Juvonen, K Amberla, et al.Neurology|August 28, 2002
Narrowing in on the causative defect of an intriguing X-linked myopathy with excessive autophagyB A Minassian, R Aiyar, S Alic, et al.Muscle & Nerve|March 1, 2005
Enrichment of the R77C alpha-sarcoglycan gene mutation in Finnish LGMD2D patientsP Hackman, V Juvonen, J Sarparanta, et al.Forensic Science International|December 17, 1998
Alzheimer changes are common in aged drivers killed in single car crashes and at intersectionsM Viitanen, K Johansson, N Bogdanovic, et al.Current Alzheimer Research|October 26, 2013
Relationships between white matter hyperintensities, cerebral amyloid angiopathy and dementia in a population-based sample of the oldest oldM Tanskanen, R N Kalaria, I-L Notkola, et al.Neuromuscular Disorders : NMD|March 17, 2004
New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2)R Sallinen, A Vihola, L L Bachinski, et al.Brain : a Journal of Neurology|January 20, 2007
Hereditary multi-infarct dementia of the Swedish type is a novel disorder different from NOTCH3 causing CADASILW C Low, M Junna, A Börjesson-Hanson, et al.Nature Medicine|April 18, 1998
A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1R Crook, A Verkkoniemi, J Perez-Tur, et al.Annals of Neurology|November 18, 2000
Variant Alzheimer's disease with spastic paraparesis and cotton wool plaques is caused by PS-1 mutations that lead to exceptionally high amyloid-beta concentrationsH Houlden, M Baker, E McGowan, et al.Pageof 21