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        - 2025
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                        Mark
        Neurocognition, Cerebellar Functions and Psychiatric Features in Spinocerebellar Ataxia Type 34
    
    
- Contribution to journal › Published meeting abstract
 
 - 2024
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                        Mark
        Clinical and genetic analyses of a Swedish patient series diagnosed with ataxia
    
    
- Contribution to journal › Article
 
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                        Mark
        Patients’ Perspective in Hereditary Ataxia
    
    
- 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
 
 - 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
    
    
- Contribution to journal › Published meeting abstract
 
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                        Mark
        Patient perspective in hereditary ataxia
    
    
- Contribution to journal › Published meeting abstract
 
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                        Mark
        Clinical and genetic studies of patients and families with ataxia
    (2023) In Lund University, Faculty of Medicine Doctoral Dissertation Series
- Thesis › Doctoral thesis (compilation)
 
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                        Mark
        Neurocognitive and cerebellar function in ADHD, autism and spinocerebellar ataxia
    
    
- Contribution to journal › Scientific review
 
 - 2022
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                        Mark
        Tau and neurofilament light-chain as fluid biomarkers in spinocerebellar ataxia type 3
    
    
- Contribution to journal › Article
 
 - 2020
 - 
                        Mark
        Toward allele-specific targeting therapy and pharmacodynamic marker for spinocerebellar ataxia type 3
    
    
- Contribution to journal › Article
 
 
