(Q70190735)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6321192%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

title

Deficiency of cytochromes b and aa3 in muscle from a floppy infant with cytochrome oxidase deficiency (English)

1 reference

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9 October 2019

6

1 reference

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9 October 2019

author name string

R C Sengers

1

1 reference

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9 October 2019

J M Trijbels

2

1 reference

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9 October 2019

J A Bakkeren

3

1 reference

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9 October 2019

W Ruitenbeek

4

1 reference

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9 October 2019

J C Fischer

5

1 reference

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9 October 2019

A M Stadhouders

7

1 reference

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9 October 2019

H J ter Laak

8

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9 October 2019

publication date

1 January 1984

1 reference

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European Journal of Pediatrics

9 October 2019

published in

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9 October 2019

volume

141

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9 October 2019

issue

3

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9 October 2019

page(s)

178-180

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Hereditary mitochondrial myopathy with lactic acidemia, a De Toni-Fanconi-Debré syndrome, and a defective respiratory chain in voluntary striated muscles

9 October 2019

cites work

1 reference

12 December 2020

Mitochondria-lipid-glycogen (MLG) disease of muscle. A morphologically regressive congenital myopathy

1 reference

12 December 2020

A mitochondrial myopathy with a defective respiratory chain and carnitine deficiency

1 reference

12 December 2020

Fatal infhntile mitochondrial myopathy and renal dysfunction due to cytochrome-c-oxidase deficiency

1 reference

12 December 2020

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

1 reference

12 December 2020

Cytochrome-C-oxidase deficiency in muscles of a floppy infant without mitochondrial myopathy

1 reference

12 December 2020

Pyruvate oxidation in rat and human skeletal muscle mitochondria

1 reference

12 December 2020

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

1 reference

12 December 2020

Cytochrome-c-oxidase deficiency in a floppy infant

1 reference

12 December 2020

Benign infantile mitochondrial myopathy due to reversible cytochrome c oxidase deficiency

1 reference

12 December 2020

Letter: A metabolic myopathy associated with chronic lactic acidemia, growth failure, and nerve deafness

1 reference

12 December 2020

Trichopoliodystrophy. I. Report of a case and biochemical studies

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00443221

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6321192%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

1 reference