Adult-onset leukodystrophies from respiratory chain disorders: do they exist? - Wikidata - awgldk - TriplyDB

Adult-onset leukodystrophies from respiratory chain disorders: do they exist?

Adult-onset leukodystrophies from respiratory chain disorders: do they exist?

http://www.wikidata.org/entity/Q30586606

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The role of brain MRI in mitochondrial neurogastrointestinal encephalomyopathy.Mitochondrial Neurogastrointestinal Encephalomyopathy Caused by Thymidine Phosphorylase Enzyme Deficiency: From Pathogenesis to Emerging Therapeutic Options.

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P2860

Adult-onset leukodystrophies from respiratory chain disorders: do they exist?

http://www.wikidata.org/entity/Q30586606

description

2013 nî lūn-bûn

@nan

2013 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի հունվարին հրատարակված գիտական հոդված

@hy

2013年の論文

@ja

2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

name

Adult-onset leukodystrophies from respiratory chain disorders: do they exist?

@ast

Adult-onset leukodystrophies from respiratory chain disorders: do they exist?

@en

type

label

Adult-onset leukodystrophies from respiratory chain disorders: do they exist?

@ast

Adult-onset leukodystrophies from respiratory chain disorders: do they exist?

@en

prefLabel

Adult-onset leukodystrophies from respiratory chain disorders: do they exist?

@ast

Adult-onset leukodystrophies from respiratory chain disorders: do they exist?

@en

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S00415-013-6844-Z

P1433

Journal of Neurology

P1476

Adult-onset leukodystrophies from respiratory chain disorders: do they exist?

@en

P2093

Davide Pareyson

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

Ettore Salsano

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

Franco Carrara

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

Franco Salerno

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

Giuseppe Piscosquito

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

Laura Farina

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

Lucia Morandi

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

Mario Savoiardo

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

P2860

A mutation in the human heme A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiency

MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion

SDHAF1, encoding a LYR complex-II specific assembly factor, is mutated in SDH-defective infantile leukoencephalopathy

Infantile encephalopathy and defective mitochondrial DNA translation in patients with mutations of mitochondrial elongation factors EFG1 and EFTu

Clinical and genetic spectrum of mitochondrial neurogastrointestinal encephalomyopathy

A mitochondrial cytochrome b mutation causing severe respiratory chain enzyme deficiency in humans and yeast

MRI of the brain in the Kearns-Sayre syndrome: report of four cases and a review.

White matter involvement in mitochondrial diseases.

Leukoencephalopathies associated with inborn errors of metabolism in adults.

Leukoencephalopathies in mitochondrial disorders: clinical and MRI findings.

P2888

s00415-013-6844-z

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1617-1623

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scholarly article

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10.1007/S00415-013-6844-Z

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P433

6

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260

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Massimo Zeviani

Costanza Lamperti

Eleonora Lamantea

Graziella Uziel

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2013-01-29T00:00:00Z

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1045689231

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23358625

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