(Q43683510)

25 November 2017

title

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

1 reference

25 November 2017

F A Wijburg

1

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25 November 2017

P G Barth

2

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25 November 2017

W Ruitenbeek

3

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25 November 2017

R J Wanders

4

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25 November 2017

G D Vos

5

1 reference

25 November 2017

S L Ploos van Amstel

6

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25 November 2017

R B Schutgens

7

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25 November 2017

publication date

1 January 1989

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Journal of Inherited Metabolic Disease

25 November 2017

published in

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25 November 2017

volume

12 Suppl 2

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25 November 2017

page(s)

349-351

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31P NMR study of improvement in oxidative phosphorylation by vitamins K3 and C in a patient with a defect in electron transport at complex III in skeletal muscle.

25 November 2017

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF03335419

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

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF03335419

DT diaphorase. II. Relation to respiratory chain of intact mitochondira

21 January 2018

1 reference

12 December 2020

NADH-CoQ reductase deficient myopathy: successful treatment with riboflavin

1 reference

12 December 2020

Childhood mitochondrial myopathy with ophthalmoplegia

1 reference

12 December 2020

Mitochondrial myopathies

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF03335419

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Dimensions Publication ID

25 November 2017

1004083072

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