Biochemical studies in mitochondrial encephalomyopathy. - Wikidata - wikimedia - TriplyDB

Biochemical studies in mitochondrial encephalomyopathy.

Biochemical studies in mitochondrial encephalomyopathy.

http://www.wikidata.org/entity/Q33629607

about

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS): current concepts

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P2860

Biochemical studies in mitochondrial encephalomyopathy.

http://www.wikidata.org/entity/Q33629607

description

1987 nî lūn-bûn

@nan

1987 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

1987 թվականի հոտեմբերին հրատարակված գիտական հոդված

@hy

1987年の論文

@ja

1987年論文

@yue

1987年論文

@zh-hant

1987年論文

@zh-hk

1987年論文

@zh-mo

1987年論文

@zh-tw

1987年论文

@wuu

name

Biochemical studies in mitochondrial encephalomyopathy.

@ast

Biochemical studies in mitochondrial encephalomyopathy.

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type

label

Biochemical studies in mitochondrial encephalomyopathy.

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Biochemical studies in mitochondrial encephalomyopathy.

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prefLabel

Biochemical studies in mitochondrial encephalomyopathy.

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Biochemical studies in mitochondrial encephalomyopathy.

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JNNP.50.10.1348

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Journal of Neurology, Neurosurgery and Psychiatry

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Biochemical studies in mitochondrial encephalomyopathy.

@en

P2093

DiMauro S

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Goda S

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Goto I

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Ishimoto S

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Koike K

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Koike M

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Kuroiwa Y

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Nakagawa M

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Reichmann H

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P2860

Retinitis pigmentosa, external ophthalmophegia, and complete heart block: unusual syndrome with histologic study in one of two cases

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.

Mitochondrial myopathy and lactic acidaemia with myoclonic epilepsy, ataxia and hypothalamic infertility: a variant of Ramsay-Hunt syndrome?

Pyruvate carboxylase and phosphoenolpyruvate carboxykinase activity in leukocytes and fibroblasts from a patient with pyruvate carboxylase deficiency.

Beta-oxidation enzymes in normal human muscle and in muscle from a patient with an unusual form of myopathic carnitine deficiency.

Striated muscle ultrastructure in intermittent claudication.

Mitochondrial encephalomyopathy with lactate-pyruvate elevation and brain infarctions.

Crystals in muscle fibers in patients with diabetic amyotrophy and neuropathy.

Reversible alexia, mitochondrial myopathy, and lactic acidemia.

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

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1348-1352

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scholarly article

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10.1136/JNNP.50.10.1348

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1987-10-01T00:00:00Z

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19481250

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3681314

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1032463

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