(Q44911329)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15164143%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

title

A case of sporadic infantile histiocytoid cardiomyopathy caused by the A8344G (MERRF) mitochondrial DNA mutation (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15164143%20AND%20SRC:MED&resulttype=core&format=json

infantile histiocytoid cardiomyopathy

29 December 2019

main subject

0 references

0 references

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15164143%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

author name string

G Jeven

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15164143%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

D C Wallace

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15164143%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

M D Brown

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15164143%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

publication date

28 May 2004

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15164143%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15164143%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

volume

25

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15164143%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15164143%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

page(s)

538-540

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15164143%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00246-003-0446-y

29 December 2019

exact match

0 references

cites work

Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency

1 reference

12 December 2020

1 reference

12 December 2020

Biochemical and molecular basis for mitochondrial cardiomyopathy in neonates and children

1 reference

12 December 2020

A missense mutation in the mitochondrial cytochrome b gene in a revisited case with histiocytoid cardiomyopathy

1 reference

12 December 2020

Sudden death in an infant due to histiocytoid cardiomyopathy. A light-microscopic, ultrastructural, and immunohistochemical study

1 reference

12 December 2020

Histiocytoid cardiomyopathy with hypotonia in an infant

1 reference

12 December 2020

Histiocytoid cardiomyopathy: three new cases and a review of the literature

1 reference

12 December 2020

Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene

1 reference

12 December 2020

Infantile histiocytoid cardiomyopathy: three cases and literature review.

1 reference

12 December 2020

Hearts of infants and children. Weights and measurements

1 reference

12 December 2020

Histiocytoid Cardiomyopathy of Infancy: Deficiency of Reducible Cytochrome b in Heart Mitochondria

1 reference

12 December 2020

10.1007/S00246-003-0446-Y

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15164143%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

1 reference