(Q68484619)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2172646%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

title

Heterogeneous tissue expression of enzyme defects in mitochondrial myopathies (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2172646%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

author name string

W Sperl

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2172646%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

W Ruitenbeek

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2172646%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

J M Trijbels

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2172646%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

G C Korenke

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2172646%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

R C Sengers

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2172646%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

publication date

1 January 1990

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2172646%20AND%20SRC:MED&resulttype=core&format=json

Journal of Inherited Metabolic Disease

24 September 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2172646%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

volume

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2172646%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2172646%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

page(s)

359-362

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2172646%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf01799395

24 September 2019

exact match

0 references

cites work

Deficiency of the alpha and beta subunits of pyruvate dehydrogenase in a patient with lactic acidosis and unexpected sudden death

1 reference

12 December 2020

Defective intramitochondrial NADH oxidation in skin fibroblasts from an infant with fatal neonatal lacticacidemia

1 reference

12 December 2020

Progressive infantile poliodystrophy (Alpers' disease) with a defect in citric acid cycle activity in liver and fibroblasts.

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

Complexity and tissue specificity of the mitochondrial respiratory chain

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

A deficiency of both subunits of pyruvate dehydrogenase which is not expressed in fibroblasts

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01799395

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2172646%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

1 reference