Middle Cerebellar Peduncle Width—A Novel MRI Biomarker for FXTAS? - Wikidata - wikimedia - TriplyDB

Middle Cerebellar Peduncle Width—A Novel MRI Biomarker for FXTAS?

Middle Cerebellar Peduncle Width—A Novel MRI Biomarker for FXTAS?

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Middle Cerebellar Peduncle Width—A Novel MRI Biomarker for FXTAS?

http://www.wikidata.org/entity/Q55516344

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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Middle Cerebellar Peduncle Width—A Novel MRI Biomarker for FXTAS?

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Middle Cerebellar Peduncle Width—A Novel MRI Biomarker for FXTAS?

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Middle Cerebellar Peduncle Width—A Novel MRI Biomarker for FXTAS?

@en

Middle Cerebellar Peduncle Width—A Novel MRI Biomarker for FXTAS?

@nl

prefLabel

Middle Cerebellar Peduncle Width—A Novel MRI Biomarker for FXTAS?

@en

Middle Cerebellar Peduncle Width—A Novel MRI Biomarker for FXTAS?

@nl

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Frontiers in Neuroscience

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Middle Cerebellar Peduncle Width—A Novel MRI Biomarker for FXTAS?

@en

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Anna Chen

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

Annie L. Shelton

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

David Hessl

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

Emilio Ferrer

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

Emily Fourie

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

Flora Tassone

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

Jun Y. Wang

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

Lauren Frizzi

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

Randi J. Hagerman

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Susan M. Rivera

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P2860

Penetrance of the fragile X-associated tremor/ataxia syndrome in a premutation carrier population

Three-dimensional tracking of axonal projections in the brain by magnetic resonance imaging

Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support

N4ITK: improved N3 bias correction

MR imaging of middle cerebellar peduncle width: differentiation of multiple system atrophy from Parkinson disease.

The primate cortico-cerebellar system: anatomy and function.

A novel FMR1 PCR method for the routine detection of low abundance expanded alleles and full mutations in fragile X syndrome.

FMR1 CGG allele size and prevalence ascertained through newborn screening in the United States

Fragile X premutation tremor/ataxia syndrome: molecular, clinical, and neuroimaging correlates.

Dementia in fragile X-associated tremor/ataxia syndrome (FXTAS): comparison with Alzheimer's disease.

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12

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2018-06-25T00:00:00Z

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6026659

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