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Human Molecular Genetics|February 3, 2000
Genetic variability in the regulatory region of presenilin 1 associated with risk for Alzheimer's disease and variable expressionJ Theuns, J Del-Favero, B Dermaut, et al.Journal of Neurology|January 5, 2002
Variable expression of presenilin 1 is not a major determinant of risk for late-onset Alzheimer's diseaseB Dermaut, G Roks, J Theuns, et al.Brain : a Journal of Neurology|November 10, 2001
Cerebral amyloid angiopathy is a pathogenic lesion in Alzheimer's disease due to a novel presenilin 1 mutationB Dermaut, S Kumar-Singh, C De Jonghe, et al.Journal of Neurology, Neurosurgery, and Psychiatry|July 24, 2003
Prospective Belgian study of neurodegenerative and vascular dementia: APOE genotype effectsS Engelborghs, B Dermaut, J Goeman, et al.American Journal of Medical Genetics|July 13, 2002
Effect of the APOE-491A/T promoter polymorphism on apolipoprotein E levels and risk of Alzheimer disease: The Rotterdam StudyG Roks, M Cruts, J J Houwing-Duistermaat, et al.Neuromuscular Disorders : NMD|February 5, 2003
Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegiaG Van Goethem, J J Martin, B Dermaut, et al.Neurology|September 12, 2000
The alpha2-macroglobulin gene in AD: a population-based study and meta-analysisM N Koster, B Dermaut, M Cruts, et al.Journal of Neurology, Neurosurgery, and Psychiatry|July 20, 2004
Octapeptide repeat insertions in the prion protein gene and early onset dementiaE A Croes, J Theuns, J J Houwing-Duistermaat, et al.Human Molecular Genetics|July 13, 1999
Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer's disease by increased Abeta42 secretionC De Jonghe, M Cruts, E A Rogaeva, et al.Journal of Neurology, Neurosurgery, and Psychiatry|December 19, 2009
Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to m.14487T>CB Dermaut, S Seneca, L Dom, et al.Pageof 3