(Q67823167)

English

NADH:Q1 oxidoreductase deficiency without lactic acidosis in a patient with leigh syndrome: Implications for the diagnosis of inborn errors of the respiratory chain

scientific article published on 01 January 1991

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1770777%20AND%20SRC:MED&resulttype=core&format=json

18 September 2019

NADH:Q1 oxidoreductase deficiency without lactic acidosis in a patient with Leigh syndrome: implications for the diagnosis of inborn errors of the respiratory chain (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1770777%20AND%20SRC:MED&resulttype=core&format=json

18 September 2019

NADH:Q1 oxidoreductase deficiency without lactic acidosis in a patient with leigh syndrome: Implications for the diagnosis of inborn errors of the respiratory chain (English)

1 reference

10.1007/BF01811686

https://api.crossref.org/works/10.1007/BF01811686

19 November 2022

lactic acidosis

1 reference

based on heuristic

inferred from title

1 reference

10.1007/BF01811686

https://api.crossref.org/works/10.1007/BF01811686

19 November 2022

author name string

F. A. Wijburg

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1770777

19 November 2022

R. J. Wanders

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1770777

19 November 2022

E. M. van Lie Peters

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1770777

19 November 2022

G. D. Vos

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1770777

19 November 2022

H. G. Loggers

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1770777

19 November 2022

P. A. Bolhuis

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1770777

19 November 2022

N. H. Herzberg

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1770777

19 November 2022

W. Ruitenbeek

8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1770777

19 November 2022

A. van Wilsem

9

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1770777

19 November 2022

R. ten Houten

10

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1770777

19 November 2022

language of work or name

1 reference

National Center for Biotechnology Information

PubMed publication ID

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1770777

19 November 2022

publication date

1 January 1991

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1770777%20AND%20SRC:MED&resulttype=core&format=json

18 September 2019

full work available at URL

http://link.springer.com/content/pdf/10.1007/BF01811686

1 reference

10.1007/BF01811686

https://api.crossref.org/works/10.1007/BF01811686

19 November 2022

Journal of Inherited Metabolic Disease

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1770777%20AND%20SRC:MED&resulttype=core&format=json

18 September 2019

14

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1770777%20AND%20SRC:MED&resulttype=core&format=json

18 September 2019

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1770777%20AND%20SRC:MED&resulttype=core&format=json

18 September 2019

297-300

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1770777%20AND%20SRC:MED&resulttype=core&format=json

18 September 2019

https://scigraph.springernature.com/pub.10.1007/bf01811686

0 references

Differential expression of nuclear genes for cytochrome c oxidase during myogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/1770777

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies on the formation of lactate and pyruvate from glucose in cultured skin fibroblasts: implications for detection of respiratory chain defects.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1770777

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterogeneous tissue expression of enzyme defects in mitochondrial myopathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/1770777

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1770777

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Free-energy carriers in human cultured muscle cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/1770777

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defects in muscle fiber growth in fatal infantile cytochrome c oxidase deficiency.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1770777

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intravenous pyruvate loading test in Leigh syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1770777

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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