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Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort
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- Journal Article
- A1
- open access
Morphological spectrum and clinical features of myopathies with tubular aggregates
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Extending the KCNQ2 encephalopathy spectrum: clinical and neuroimaging findings in 17 patients
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A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum : a gene identification study
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KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy
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Ataxin-2 polyQ expansions in FTLD-ALS spectrum disorders in Flanders-Belgian cohorts
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Distinct clinical characteristics of C9orf72 expansion carriers compared to GRN, MAPT and non-mutation carries in a Flanders-Belgian FTLD cohort
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Mutant HSPB8 causes protein aggregates and a reduced mitochondrial membrane potential in dermal fibroblasts from distal hereditary motor neuropathy patients
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Mutant HSPB8 causes motor neuron-specific neurite degeneration
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Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS