(Q38635118)

5 September 2017

1 reference

title

Mitochondria-related encephalomyopathies (English)

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5 September 2017

Goebel HH

1

1 reference

5 September 2017

Bornemann A

series ordinal

2

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5 September 2017

Reichmann H

series ordinal

3

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5 September 2017

publication date

1 March 1989

1 reference

Neuropathology and Applied Neurobiology

5 September 2017

published in

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5 September 2017

volume

15

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5 September 2017

issue

2

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5 September 2017

page(s)

97-119

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Sequence and organization of the human mitochondrial genome

5 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Childhood encephalomyopathy with cytochrome c oxidase deficiency, ataxia, muscle wasting, and mental impairment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Cytochrome c oxidase deficiency in subacute necrotizing encephalomyelopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Mitochondrial myopathy--a result of clofibrate/etofibrate treatment? Case report

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Electron cytochemistry of crystalline inclusions in human skeletal muscle mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

"Cerebral" lactic acidosis: defects in pyruvate metabolism with profound brain damage and minimal systemic acidosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Mitochondrial myoneuropathy with respiratory failure and myoclonic epilepsy. A case report with biochemical studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH dehydrogenase

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

URF6, last unidentified reading frame of human mtDNA, codes for an NADH dehydrogenase subunit

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Fatal ataxic encephalopathy and carnitine acetyltransferase deficiency: A functional defect of pyruvate oxidation?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Pyruvate decarboxylase deficiency in subacute necrotizing encephalomyelopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

A mitochondrial encephalomyopathy: the first case with an established defect at the level of coenzyme Q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Trichopoliodystrophy. I. Report of a case and biochemical studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Maternal inheritance of human mitochondrial DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Sural nerve biopsy studies in Leigh's subacute necrotizing encephalomyelopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

The occurrence of paracrystalline mitochondrial inclusions in normal human skeletal muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Progressive neuronal degeneration of childhood with liver disease. A pathological study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Kearns-Sayre syndrome with hypoparathyroidism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Retinitis Pigmentosa, External Ophthalmoplegia, and Complete Heart Block

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Mitochondrial cytopathy with lactic acidosis, carnitine deficiency and DeToni-Fanconi-Debré syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical, and morphological study

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Aspartoacylase deficiency and N-acetylaspartic aciduria in patients with canavan disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Involvement of choroid plexus in mitochondrial encephalomyopathy (MELAS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Oculocraniosomatic neuromuscular disease with "ragged-red" fibers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Progressive poliodystrophy (Alpers' disease) with a defect in cytochrome aa3 in muscle: a report of two unrelated patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Deficiency of Dihydrolipoyl Dehydrogenase (a Component of the Pyruvate and α-Ketoglutarate Dehydrogenase Complexes): A Cause of Congenital Chronic Lactic Acidosis in Infancy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Clinical presentation of mitochondrial respiratory chain defects in NADH-coenzyme Q reductase and cytochrome oxidase: clues to pathogenesis of Leigh disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Maternally inherited mitochondrial myopathy and myoclonic epilepsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Defects in oxidative phosphorylation. Biochemical investigations in skeletal muscle and expression of the lesion in other cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Neuromuscular Disorder Associated With a Defect in Mitochondrial Energy Supply

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

A mitochondrial myopathy with a defective respiratory chain and carnitine deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Secondary mitochondrial pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Mitochondrial encephalomyopathy and partial cytochrome c oxidase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Familial poliodystrophy, mitochondrial myopathy, and lactate acidemia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Morphological observations in skeletal muscle from patients with a mitochondrial myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Peripheral nerve lesion in spongy degeneration of the central nervous system.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Are there two forms of carnitine palmitoyltransferase in muscle?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Fumarase deficiency: a new cause of mitochondrial encephalomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Myo-, neuro-, gastrointestinal encephalopathy (MNGIE syndrome) due to partial deficiency of cytochrome-c-oxidase

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Enzymic Activities of Human Skeletal Muscle Mitochondria: A Tool in Clinical Metabolic Research

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1989.TB01214.X

10.1111/J.1365-2990.1989.TB01214.X

21 January 2018

Identifiers

DOI

1 reference

release_4fudimqxmffjtdsio7whugwdhe

5 September 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/4fudimqxmffjtdsio7whugwdhe

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference