(Q79327256)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17082968%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

title

Succinate dehydrogenase deficiency associated with dilated cardiomyopathy and ventricular noncompaction (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17082968%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

main subject

dilated cardiomyopathy

1 reference

Zurab Davili

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17082968%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

Sandeep Johar

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17082968%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

Colleen Hughes

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17082968%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

Daniel Kveselis

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17082968%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

Joe Hoo

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17082968%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

publication date

3 November 2006

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17082968%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Pediatrics

21 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17082968%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

volume

166

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17082968%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

issue

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17082968%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

page(s)

867-870

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17082968%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00431-006-0310-1

21 December 2019

exact match

0 references

cites work

Isolated complex I deficiency in children: clinical, biochemical and genetic aspects

1 reference

12 December 2020

Mitochondrial myopathy with lactic acidosis and deficient activity of muscle succinate cytochrome-c-oxidoreductase

1 reference

12 December 2020

A novel X-linked gene, G4.5. is responsible for Barth syndrome

1 reference

12 December 2020

The oxidative phosphorylation (OXPHOS) system: nuclear genes and human genetic diseases

1 reference

12 December 2020

The emerging concept of mitochondrial cardiomyopathies

1 reference

12 December 2020

Combined 3-methylglutaconic and 3-hydroxy-3-methylglutaric aciduria with endocardial fibroelastosis and dilatative cardiomyopathy in male and female siblings with partial deficiency of complex II/III in fibroblasts

1 reference

12 December 2020

The investigation of respiratory chain disorders in heart using endomyocardial biopsies

1 reference

12 December 2020

Deficiency of complex II of the mitochondrial respiratory chain in late-onset optic atrophy and ataxia

1 reference

12 December 2020

Myocardial gene expression in dilated cardiomyopathy treated with beta-blocking agents

1 reference

12 December 2020

Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome

1 reference

12 December 2020