Abnormal kinetic behavior of cytochrome oxidase in a case of Leigh disease (Q35199469)

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Language	Label	Description	Also known as
English	Abnormal kinetic behavior of cytochrome oxidase in a case of Leigh disease	scientific article

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scholarly article

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Europe PubMed Central

PMC publication ID

1684310

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2821802%20AND%20SRC:MED&resulttype=core&format=json

retrieved

5 October 2019

title

Abnormal kinetic behavior of cytochrome oxidase in a case of Leigh disease (English)

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stated in

Europe PubMed Central

PMC publication ID

1684310

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2821802%20AND%20SRC:MED&resulttype=core&format=json

retrieved

5 October 2019

main subject

Leigh disease

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inferred from title

author name string

Glerum M

series ordinal

1

1 reference

stated in

Europe PubMed Central

PMC publication ID

1684310

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2821802%20AND%20SRC:MED&resulttype=core&format=json

retrieved

5 October 2019

Robinson BH

series ordinal

2

1 reference

stated in

Europe PubMed Central

PMC publication ID

1684310

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2821802%20AND%20SRC:MED&resulttype=core&format=json

retrieved

5 October 2019

Spratt C

series ordinal

3

1 reference

stated in

Europe PubMed Central

PMC publication ID

1684310

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2821802%20AND%20SRC:MED&resulttype=core&format=json

retrieved

5 October 2019

Wilson J

series ordinal

4

1 reference

stated in

Europe PubMed Central

PMC publication ID

1684310

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2821802%20AND%20SRC:MED&resulttype=core&format=json

retrieved

5 October 2019

Patrick D

series ordinal

5

1 reference

stated in

Europe PubMed Central

PMC publication ID

1684310

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2821802%20AND%20SRC:MED&resulttype=core&format=json

retrieved

5 October 2019

language of work or name

English

0 references

publication date

1 October 1987

1 reference

stated in

Europe PubMed Central

PMC publication ID

1684310

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2821802%20AND%20SRC:MED&resulttype=core&format=json

retrieved

5 October 2019

published in

American Journal of Human Genetics

1 reference

stated in

Europe PubMed Central

PMC publication ID

1684310

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2821802%20AND%20SRC:MED&resulttype=core&format=json

retrieved

5 October 2019

volume

41

1 reference

stated in

Europe PubMed Central

PMC publication ID

1684310

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2821802%20AND%20SRC:MED&resulttype=core&format=json

retrieved

5 October 2019

issue

4

1 reference

stated in

Europe PubMed Central

PMC publication ID

1684310

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2821802%20AND%20SRC:MED&resulttype=core&format=json

retrieved

5 October 2019

page(s)

584-593

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Europe PubMed Central

PMC publication ID

1684310

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2821802%20AND%20SRC:MED&resulttype=core&format=json

retrieved

5 October 2019

cites work

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PubMed Central

reference URL

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Mitochondrial respiratory control. Evidence against the regulation of respiration by extramitochondrial phosphorylation potentials or by [ATP]/[ADP] ratios

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Deficiency of the iron-sulfur clusters of mitochondrial reduced nicotinamide-adenine dinucleotide-ubiquinone oxidoreductase (complex I) in an infant with congenital lactic acidosis

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13 July 2018

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13 July 2018

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

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13 July 2018

Investigation of mitochondrial metabolism in small human skeletal muscle biopsy specimens. Improvement of preparation procedure.

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13 July 2018

Respiratory chain defects in the mitochondria of cultured skin fibroblasts from three patients with lacticacidemia

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13 July 2018

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

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PubMed Central

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13 July 2018

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

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28 July 2018

Two siblings with cytochromec oxidase deficiency

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26 September 2018

Oxidative phosphorylation in mitochondria isolated from human fibroblasts

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12 December 2020

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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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2821802

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12 December 2020

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

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2821802

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12 December 2020

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The genetic heterogeneity of lactic acidosis: occurrence of recognizable inborn errors of metabolism in pediatric population with lactic acidosis

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2821802

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12 December 2020

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Cytochrome-c-oxidase deficiency in a floppy infant

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2821802

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12 December 2020

based on heuristic

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Fatal lipid storage myopathy with deficiency of cytochrome-c-oxidase and carnitine. A contribution to the combined cytochemical-finestructural identification of cytochrome-c-oxidase in longterm frozen muscle

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/2821802

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12 December 2020

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Demyelination and disturbed metabolism of pyruvate: a case report

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2821802

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Benign infantile mitochondrial myopathy due to reversible cytochrome c oxidase deficiency

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2821802

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2821802

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1684310

1 reference

stated in

Europe PubMed Central

PMC publication ID

1684310

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2821802%20AND%20SRC:MED&resulttype=core&format=json

retrieved

5 October 2019

PubMed publication ID

2821802

1 reference

stated in

Europe PubMed Central

PMC publication ID

1684310

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2821802%20AND%20SRC:MED&resulttype=core&format=json

retrieved

5 October 2019

 

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