Andreas Puschmann
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- 2020
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Mark
Disappearance of familially aggregated paralysis agitans in subsequent generations: a 135-year follow up study
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- Contribution to journal › Published meeting abstract
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Mark
Long term outcome of Parkinson’s disease and validation of a new clinical classification system.
(
- Contribution to journal › Published meeting abstract
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Mark
Ataxia project in Scania, Sweden: Study outline and current status
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- Contribution to journal › Published meeting abstract
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Mark
Co-occurrence of leukoencephalopathy with ataxia and SPG56 in one family
(
- Contribution to journal › Published meeting abstract
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Mark
Toward allele-specific targeting therapy and pharmacodynamic marker for spinocerebellar ataxia type 3
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- Contribution to journal › Article
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Mark
Do variants in IRF2BPL cause both neurological disorders and keratoconus 8?
(
- Contribution to journal › Debate/Note/Editorial
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Mark
Abstracts of the IAPRD XXV World Congress on Parkinson's Disease and Related Disorders, 2020. Congress theme : Diagnosing and treating movement disorders in the era of personalized medicine
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- Contribution to journal › Debate/Note/Editorial
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Mark
Whole-Exome Sequencing in 22 Young Ischemic Stroke Patients With Familial Clustering of Stroke
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- Contribution to journal › Article
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Mark
New generation genetic testing entering the clinic
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- Contribution to journal › Article
- 2019
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Mark
Nationwide prevalence of primary dystonia, progressive ataxia and hereditary spastic paraplegia
(
- Contribution to journal › Article