2016 in Review and Message from the Editors to our Reviewers.

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2016 in Review and Message from the Editors to our Reviewers.

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2017 nî lūn-bûn

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2017年の論文

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2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

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2017年论文

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2017年论文

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2016 in Review and Message from the Editors to our Reviewers.

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2016 in Review and Message from the Editors to our Reviewers.

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2016 in Review and Message from the Editors to our Reviewers.

@en

2016 in Review and Message from the Editors to our Reviewers.

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2016 in Review and Message from the Editors to our Reviewers.

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2016 in Review and Message from the Editors to our Reviewers.

@nl

P1476

2016 in Review and Message from the Editors to our Reviewers.

@en

P2093

Jeffery M Vance

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Massimo Pandolfo

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Nicholas Elwood Johnson

http://www.w3.org/2001/XMLSchema#string

Raymond P Roos

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Stefan M Pulst

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P2860

Genetic Misdiagnoses and the Potential for Health Disparities

Novel genetic loci underlying human intracranial volume identified through genome-wide association

Parkinson-associated risk variant in distal enhancer of α-synuclein modulates target gene expression

The C9orf72 repeat expansion disrupts nucleocytoplasmic transport.

GGGGCC repeat expansion in C9orf72 compromises nucleocytoplasmic transport.

Intrathecal gene therapy rescues a model of demyelinating peripheral neuropathy.

APOE polymorphisms influence longitudinal lipid trends preceding intracerebral hemorrhage

The Clinical Outcome Study for dysferlinopathy: An international multicenter study.

White matter lesions in FTLD: distinct phenotypes characterize GRN and C9ORF72 mutations.

White matter involvement in a family with a novel PDGFB mutation.

P304

e132

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P31

scholarly article

editorial

P356

10.1212/NXG.0000000000000132

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P433

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P478

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P50

Alexandra Durr

P577

2017-02-15T00:00:00Z

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P698

28251178

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P932

5314733

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