Andreas Puschmann
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- 2023
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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
-
Mark
Co-occurrence of CLCN2-related leukoencephalopathy and SPG56
- Contribution to journal › Article
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Mark
Substitution of PINK1 Gly411 modulates substrate receptivity and turnover
- Contribution to journal › Article
-
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
-
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
Insights on Genetic and Environmental Factors in Parkinson's Disease from a Regional Swedish Case-Control Cohort
- Contribution to journal › Article
-
Mark
A relatively common hypomorphic variant in WARS2 causes monogenic disease
- Contribution to journal › Debate/Note/Editorial
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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
-
Mark
The Interaction between HLA-DRB1 and Smoking in Parkinson's Disease Revisited
- Contribution to journal › Article
