Vanishing white matter disease in a spanish population. - Wikidata - awgldk - TriplyDB

Vanishing white matter disease in a spanish population.

Vanishing white matter disease in a spanish population.

http://www.wikidata.org/entity/Q34432161

about

Astrocytes are central in the pathomechanisms of vanishing white matter Case Report: Cerebral leukodystrophy and the gonadal endocrinopathy: a rare but real association.

P2860

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P2860

Vanishing white matter disease in a spanish population.

http://www.wikidata.org/entity/Q34432161

description

2014 nî lūn-bûn

@nan

2014 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի հուլիսին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

Vanishing white matter disease in a spanish population.

@ast

Vanishing white matter disease in a spanish population.

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Vanishing white matter disease in a spanish population.

@nl

type

label

Vanishing white matter disease in a spanish population.

@ast

Vanishing white matter disease in a spanish population.

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Vanishing white matter disease in a spanish population.

@nl

prefLabel

Vanishing white matter disease in a spanish population.

@ast

Vanishing white matter disease in a spanish population.

@en

Vanishing white matter disease in a spanish population.

@nl

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P1433

Journal of Central Nervous System Disease

P1476

Vanishing white matter disease in a spanish population

@en

P2093

Concha Sierra-Córcoles

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

David Conejo Moreno

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

Eduardo López-Laso

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

Eulàlia Turón-Viñas

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

Javier Aguirre-Rodríguez

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

Judith Armstrong-Moron

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

Luis González Gutiérrez-Solana

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

Mar O'Callaghan

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Marcos Madruga-Garrido

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Mercè Pineda

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P2860

A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation

Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter

Leukoencephalopathy with vanishing white matter: from magnetic resonance imaging pattern to five genes

Leukodystrophies: clinical and genetic aspects

[Non specific leukodystrophy. A new case of vacuolizing leukoencephalopathy with megalencephaly].

Childhood ataxia with CNS hypomyelination/vanishing white matter disease--a common leukodystrophy caused by abnormal control of protein synthesis.

Vanishing white matter disease.

Vanishing white matter disease: a review with focus on its genetics.

The spectrum of mutations for the diagnosis of vanishing white matter disease.

Decreased asialotransferrin in cerebrospinal fluid of patients with childhood-onset ataxia and central nervous system hypomyelination/vanishing white matter disease.

P304

59-68

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scholarly article

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10.4137/JCNSD.S13540

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P478

6

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2014-07-13T00:00:00Z

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264502041

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25089094

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4116383

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