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- 2024
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Mark
Clinical and genetic analyses of a Swedish patient series diagnosed with ataxia
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- Contribution to journal › Article
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Mark
Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4 : A poly-glycine disease
(
- Contribution to journal › Article
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Mark
Small vessel disease in primary familial brain calcification with novel truncating PDGFB variants
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- Contribution to journal › Article
- 2023
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Mark
LINE-1 retrotransposons drive human neuronal transcriptome complexity and functional diversification
(
- Contribution to journal › Article
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Mark
Predictive value of diffusion MRI-based parametric response mapping for prognosis and treatment response in glioblastoma
(
- Contribution to journal › Article
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Mark
Genomic analyses of a large Swedish multi-incident kindred with autosomal dominant Parkinson’s disease with dementia
(
- Contribution to journal › Published meeting abstract
- 2022
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Mark
Structural association between heterotopia and cortical lesions visualized with 7T MRI in patients with focal epilepsy
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- Contribution to journal › Article
- 2021
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Mark
Genotype–Phenotype Relations for the Atypical Parkinsonism Genes : MDSGene Systematic Review
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- Contribution to journal › Scientific review
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Mark
MAP3K6 Mutations in a Neurovascular Disease Causing Stroke, Cognitive Impairment, and Tremor
(
- Contribution to journal › Article
- 2020
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Mark
Evaluation of small nerve fiber dysfunction in type 2 diabetes
(
- Contribution to journal › Article