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
(
- 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
Genomic analyses of a large Swedish multi-incident kindred with autosomal dominant Parkinson’s disease with dementia
(
- Contribution to journal › Published meeting abstract
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Mark
Varicella-zoster virus vasculopathy in a patient with multiple sclerosis receiving natalizumab
(
- 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
(
- 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
(
- Contribution to journal › Article
- 2022
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Mark
A relatively common hypomorphic variant in WARS2 causes monogenic disease
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- Contribution to journal › Debate/Note/Editorial
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Mark
Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke
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- Contribution to journal › Article
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Mark
Patients’ Perspective in Hereditary Ataxia
2022) In Cerebellum(
- Contribution to journal › Article
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Mark
Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease: Evidence from the COURAGE-PD Consortium
(
- Contribution to journal › Article