prof. dr. Bart Dermaut
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A novel presenilin 1 mutation (gly183val) is associated with Pick's disease in the absence of β-amyloid plaques
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Neuropathological and biochemical characterization of a familial FTD patient carrying PS1 GLY183VAL
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Mutation analysis of candidate genes for chromosome 17-linked tau-negative FTD
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Dose dependent effect of APOE ε4 on behavioral symptoms in frontal lobe dementia patients
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Tau (MAPT) mutation Arg406Trp presenting clinically with Alzheimer disease does not share a common founder in western Europe
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Novel APP mutation V715A associated with presenile Alzheimer's disease in a German family
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Absence of association between codon 129/219 polymorphisms of the prion protein gene and Alzheimer's disease in Japan: reply
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Early cognitive decline is associated with prion protein codon 129 polymorphism
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Digenic progressive external ophthalmoplegiain a sporadic patient: recessive mutationsin POLG and C10orf2/Twinkle
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Prospective Belgian study of neurodegenerative and vascular dementia: APOE genotype effects