(Q44937716)

7 December 2017

title

Isolated and combined deficiencies of NADH dehydrogenase (complex I) in muscle tissue of children with mitochondrial myopathies (English)

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7 December 2017

G C Korenke

1

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7 December 2017

H A Bentlage

2

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7 December 2017

W Ruitenbeek

3

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7 December 2017

R C Sengers

4

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7 December 2017

W Sperl

5

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7 December 2017

J M Trijbels

6

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7 December 2017

F J Gabreels

7

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7 December 2017

F A Wijburg

8

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7 December 2017

V Wiedermann

9

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7 December 2017

F Hanefeld

10

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7 December 2017

language of work or name

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1 December 1990

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European Journal of Pediatrics

7 December 2017

published in

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7 December 2017

volume

150

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7 December 2017

issue

2

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7 December 2017

page(s)

104-108

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https://scigraph.springernature.com/pub.10.1007/bf02072049

7 December 2017

exact match

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cites work

Mitochondrial myopathies: deficiencies localized to complex I and complex III of the mitochondrial respiratory chain.

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF02072049

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes with recurrent abdominal symptoms and coenzyme Q10 administration

21 January 2018

1 reference

12 December 2020

A microspectrophotometric method for the determination of cytochrome oxidase.

1 reference

12 December 2020

Familial mitochondrial myopathy associated with peripheral neuropathy: partial deficiencies of complex I and complex IV

1 reference

12 December 2020

Disturbed oxidative metabolism in subacute necrotizing encephalomyelopathy (Leigh syndrome).

1 reference

12 December 2020

A mitochondrial myopathy with a deficiency of respiratory chain NADH-CoQ reductase activity

1 reference

12 December 2020

Findings in muscle in complex I (NADH coenzyme Q reductase) deficiency

1 reference

12 December 2020

Partial deficiency of subunits in complex I or IV of patients with mitochondrial myopathies

1 reference

12 December 2020

Mitochondrial Myopathy with Partial Cytochrome Oxidase Deficiency and Impaired Oxidation of NADH-Linked Substrates

1 reference

12 December 2020

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

1 reference

12 December 2020

Variability in the activity of respiratory chain enzymes in mitochondrial myopathies

1 reference

12 December 2020

Progressive infantile poliodystrophy. Association with disturbed pyruvate oxidation in muscle and liver

1 reference

12 December 2020

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

1 reference

12 December 2020

Deficiency of subunits of Complex I and mitochondrial encephalomyopathy

1 reference

12 December 2020

Two cases of NADH-coenzyme Q reductase deficiency: relationship to MELAS syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

A defect in mitochondrial electron-transport activity (NADH-coenzyme Q oxidoreductase) in Leber's hereditary optic neuropathy.

1 reference

12 December 2020

Deficiency of subunits in heart mitochondrial NADH-ubiquinone oxidoreductase of a patient with mitochondrial encephalomyopathy and cardiomyopathy.

1 reference

12 December 2020

Mitochondrial myopathy. Biochemical studies revealing a deficiency of NADH--cytochrome b reductase activity

1 reference

12 December 2020

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

1 reference

12 December 2020

NADH-CoQ reductase deficient myopathy: successful treatment with riboflavin

1 reference

12 December 2020

The clinical features of mitochondrial myopathy.

1 reference

12 December 2020

Benign mitochondrial myopathy with deficiency of NADH-CoQ reductase and cytochrome c oxidase

1 reference

12 December 2020

Familial NADH: Q1 oxidoreductase (complex I) deficiency: variable expression and possible treatment

1 reference

12 December 2020

Protein measurement with the Folin phenol reagent

1 reference

12 December 2020

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

1 reference

12 December 2020

MELAS, myoclonus, ataxia and deficiencies of complexes I and IV in muscle mitochondria.

1 reference

12 December 2020

Molecular defects of NADH-ubiquinone oxidoreductase (complex I) in mitochondrial diseases

1 reference

12 December 2020

Tissue specific defect of complex I of the mitochondrial respiratory chain

1 reference

12 December 2020

Molecular basis of mitochondrial myopathies: polypeptide analysis in complex-I deficiency

1 reference

12 December 2020

Defects in citric acid cycle and the electron transport chain in progressive poliodystrophy.

1 reference

12 December 2020

Biochemical and molecular aspects of cytochrome C oxidase deficiency.

1 reference

12 December 2020

Mitochondrial complex I deficiency in Parkinson's disease

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF02072049

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7 December 2017

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