Andreas Puschmann
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- 2023
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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
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Mark
Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers
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- Contribution to journal › Article
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Mark
Embracing Monogenic Parkinson's Disease : The MJFF Global Genetic PD Cohort
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- Contribution to journal › Article
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Mark
Whole exome sequencing of familial, combined or complex dystonia
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- Contribution to journal › Published meeting abstract
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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
Substitution of PINK1 Gly411 modulates substrate receptivity and turnover
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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
(
- Contribution to journal › Article