(Q39567226)

13 September 2017

1 reference

title

Disorders of the mitochondrial respiratory chain: clinical manifestations and diagnostic approach (English)

1 reference

13 September 2017

J M Trijbels

1

1 reference

13 September 2017

R C Sengers

2

1 reference

13 September 2017

W Ruitenbeek

3

1 reference

13 September 2017

J C Fischer

4

1 reference

13 September 2017

J A Bakkeren

5

1 reference

13 September 2017

A J Janssen

6

1 reference

13 September 2017

publication date

1 November 1988

1 reference

European Journal of Pediatrics

13 September 2017

published in

1 reference

13 September 2017

volume

148

1 reference

13 September 2017

issue

2

1 reference

13 September 2017

page(s)

92-97

1 reference

https://scigraph.springernature.com/pub.10.1007/bf00445910

13 September 2017

exact match

0 references

cites work

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

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF00445910

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

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF00445910

Blood sampling technique for lactate and pyruvate estimation in children

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF00445910

Biochemical studies in the liver and muscle of patients with Zellweger syndrome.

21 January 2018

1 reference

12 December 2020

A microspectrophotometric method for the determination of cytochrome oxidase.

1 reference

12 December 2020

Microdetermination of (-)carnitine and carnitine acetyltransferase activity

1 reference

12 December 2020

A mitochondrial myopathy with a defective respiratory chain and carnitine deficiency

1 reference

12 December 2020

Mitochondrial myopathies. Clinical, morphological and biochemical aspects

1 reference

12 December 2020

Mitochondrial inheritance in a mitochondrially mediated disease

1 reference

12 December 2020

Differential investigation of the capacity of succinate oxidation in human skeletal muscle

1 reference

12 December 2020

Lactic Acidosis and Mitochondrial Myopathy Associated with Deficiency of Several Components of Complex III of the Respiratory Chain

1 reference

12 December 2020

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

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

Peroxisomal and mitochondrial defects in the cerebro-hepato-renal syndrome

1 reference

12 December 2020

Estimation of energy metabolism in human skeletal muscle homogenate as a diagnostic aid

1 reference

12 December 2020

Estimation of NADH oxidation in human skeletal muscle mitochondria.

1 reference

12 December 2020

Friedreich's ataxia: intravenous pyruvate load to demonstrate a defect in pyruvate metabolism

1 reference

12 December 2020

Mitochondrial myopathies

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00445910

1 reference

release_bduhydtdwzdnbk2m3ui5lwlpti

13 September 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/bduhydtdwzdnbk2m3ui5lwlpti

24 November 2022

mapped directly with Wikidata item

1 reference