Clinical Neurogenetics
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- 2023
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Mark
A Swedish SCA34 family with late onset ataxia, cerebellar atrophy and ocular movement abnormalities with a novel mutation in ELOVL4
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- Contribution to journal › Published meeting abstract
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Mark
Patient perspective in hereditary ataxia
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- Contribution to journal › Published meeting abstract
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Mark
Genomic analyses of a large Swedish multi-incident kindred with autosomal dominant Parkinson’s disease with dementia
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- Contribution to journal › Published meeting abstract
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Mark
Neurocognitive and cerebellar function in ADHD, autism and spinocerebellar ataxia
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- Contribution to journal › Scientific review
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Mark
Sag-rad : A Method for Single-Cell Population Genomics of Unicellular Eukaryotes
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- Contribution to journal › Article
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Mark
Co-occurrence of CLCN2-related leukoencephalopathy and SPG56
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- Contribution to journal › Article
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Mark
Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson’s Disease Project
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- Contribution to journal › Article
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Mark
Varicella-zoster virus vasculopathy in a patient with multiple sclerosis receiving natalizumab
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- Contribution to journal › Article
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Mark
The α-synuclein PET tracer [18F] ACI-12589 distinguishes multiple system atrophy from other neurodegenerative diseases
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- Contribution to journal › Article
- 2022
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Mark
Insights on Genetic and Environmental Factors in Parkinson's Disease from a Regional Swedish Case-Control Cohort
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- Contribution to journal › Article