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- 2026
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Mark
Alexi utan agrafi – att inte kunna läsa vad man själv har skrivit
- Contribution to specialist publication or newspaper › Specialist publication article
- 2025
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Mark
Neurocognition, cerebellar functions and psychiatric features in spinocerebellar ataxia type 34 : a case series
- Contribution to journal › Article
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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
Maculopathy and adult-onset ataxia in patients with biallelic MFSD8 variants
- Contribution to journal › Article
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Mark
Spinocerebellar Ataxia Type 4
(2024) p.1-24
- Chapter in Book/Report/Conference proceeding › Book chapter
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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
