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- 2019
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Mark
Low prevalence of known pathogenic mutations in dominant PD genes : A Swedish multicenter study
(
- Contribution to journal › Article
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Mark
Nationwide prevalence of primary dystonia, progressive ataxia and hereditary spastic paraplegia
(
- Contribution to journal › Article
- 2018
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Mark
Will FTLD-tau work for all when FTDP-17 retires?
(
- Contribution to journal › Article
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Mark
Tidig diagnos och behandling med gallsyra avgörande vid cerebrotendinös xantomatos
(
- Contribution to journal › Debate/Note/Editorial
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Mark
SAMD9 and SAMD9L in inherited predisposition to ataxia, pancytopenia, and myeloid malignancies
(
- Contribution to journal › Article
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Mark
LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies : a genome-wide linkage and sequencing study
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- Contribution to journal › Article
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Mark
Slowly progressive dementia caused by MAPT R406W mutations : Longitudinal report on a new kindred and systematic review
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- Contribution to journal › Article
- 2017
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Mark
Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS and neurological symptoms
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- Contribution to journal › Article
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Mark
Heterozygous PINK1 p.G411S increases risk of Parkinson's disease via a dominant-negative mechanism
(
- Contribution to journal › Article
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Mark
New Genes Causing Hereditary Parkinson’s Disease or Parkinsonism
(
- Contribution to journal › Scientific review