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- Miscellaneous
- open access
Homozygous and compound heterozygous rare variants in VPS13C contribute to Lewy body diseases
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- Journal Article
- A1
- open access
Mutated ATP10B increases Parkinson's disease risk by compromising lysosomal glucosylceramide export
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Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to the m.14487T>C mutation in ND6
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Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family
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Influence of the prion protein and the apolipoprotein E genotype on the Creutzfeldt-Jakob disease phenotype