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- 2024
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Mark
Clinical and genetic analyses of a Swedish patient series diagnosed with ataxia
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- Contribution to journal › Article
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Mark
Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4 : A poly-glycine disease
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- Contribution to journal › Article
- 2023
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Mark
[18F]RO948 tau positron emission tomography in genetic and sporadic frontotemporal dementia syndromes
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- Contribution to journal › Article
- 2020
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Mark
Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis
(
- Contribution to journal › Article
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Mark
C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts
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- Contribution to journal › Article
- 2019
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Mark
Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia
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- Contribution to journal › Article