A mitochondrial encephalomyopathy with a partial cytochrome c oxidase deficiency of muscle - Wikidata - wikimedia - TriplyDB

A mitochondrial encephalomyopathy with a partial cytochrome c oxidase deficiency of muscle

A mitochondrial encephalomyopathy with a partial cytochrome c oxidase deficiency of muscle

http://www.wikidata.org/entity/Q33631123

about

Activity rating scales in adult muscle disease: what do they actually measure?Demonstration of two isoforms of subunit VIIa of cytochrome c oxidase from human skeletal muscle. Implications for mitochondrial myopathies.β-Turns as structural motifs for the proteolytic processing of seed proteins

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P2860

A mitochondrial encephalomyopathy with a partial cytochrome c oxidase deficiency of muscle

http://www.wikidata.org/entity/Q33631123

description

1988 nî lūn-bûn

@nan

1988 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

1988 թվականի մայիսին հրատարակված գիտական հոդված

@hy

1988年の論文

@ja

1988年論文

@yue

1988年論文

@zh-hant

1988年論文

@zh-hk

1988年論文

@zh-mo

1988年論文

@zh-tw

1988年论文

@wuu

name

A mitochondrial encephalomyopa ...... c oxidase deficiency of muscle

@ast

A mitochondrial encephalomyopa ...... c oxidase deficiency of muscle

@en

type

label

A mitochondrial encephalomyopa ...... c oxidase deficiency of muscle

@ast

A mitochondrial encephalomyopa ...... c oxidase deficiency of muscle

@en

prefLabel

A mitochondrial encephalomyopa ...... c oxidase deficiency of muscle

@ast

A mitochondrial encephalomyopa ...... c oxidase deficiency of muscle

@en

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P1433

Journal of Neurology, Neurosurgery and Psychiatry

P1476

A mitochondrial encephalomyopa ...... c oxidase deficiency of muscle

@en

P2093

Gabreëls FJ

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Renier WO

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Ruitenbeek W

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Stadhouders AM

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Ter Laak HJ

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Van Erven PM

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P2860

Protein measurement with the Folin phenol reagent

Sequence and organization of the human mitochondrial genome

Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities ): disease entity or a syndrome? Light-and electron-microscopic studies of two cases and review of literature.

Cytochrome oxidase deficiency: clinical and biochemical heterogeneity.

Subacute necrotizing encephalomyelopathy (LEIGH).

Leigh's encephalomyelopathy in a patient with cytochrome c oxidase deficiency in muscle tissue.

Mitochondrial myopathies. Clinical, morphological and biochemical aspects.

Measurement of cytochromes in human skeletal muscle mitochondria, isolated from fresh and frozen stored muscle specimens.

Subacute necrotizing encephalomyelopathy (Leigh syndrome) associated with disturbed oxidation of pyruvate, malate and 2-oxoglutarate in muscle and liver.

Fatal infantile cytochrome c oxidase deficiency: decrease of immunologically detectable enzyme in muscle.

P304

704-708

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scholarly article

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10.1136/JNNP.51.5.704

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5

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51

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1988-05-01T00:00:00Z

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20315671

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2841425

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1033081

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