X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): respiratory-chain abnormalities in cultured fibroblasts (Q71345292)

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scientific article published on 01 January 1996

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Language	Label	Description	Also known as
English	X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): respiratory-chain abnormalities in cultured fibroblasts	scientific article published on 01 January 1996

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8739954

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8739954%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

title

X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): respiratory-chain abnormalities in cultured fibroblasts (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8739954

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8739954%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

main subject

Barth syndrome

1 reference

based on heuristic

inferred from title

author name string

P G Barth

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8739954

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8739954%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

C Van den Bogert

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8739954

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8739954%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

P A Bolhuis

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8739954

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8739954%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

H R Scholte

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8739954

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8739954%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

A H van Gennip

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8739954

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8739954%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

R B Schutgens

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8739954

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8739954%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

A G Ketel

series ordinal

7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8739954

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8739954%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

publication date

1 January 1996

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8739954

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8739954%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

published in

Journal of Inherited Metabolic Disease

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8739954

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8739954%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

volume

19

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8739954

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8739954%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

issue

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8739954

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8739954%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

page(s)

157-160

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8739954

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8739954%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

cites work

X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8739954

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Barth syndrome: clinical features and confirmation of gene localisation to distal Xq28.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8739954

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Altered kinetics of cytochrome c oxidase in a patient with severe mitochondrial encephalomyopathy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8739954

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the separation of proteins in the range from 1 to 100 kDa

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8739954

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple syndromes of 3-methylglutaconic aciduria

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8739954

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8739954

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Barth syndrome: clinical observations and genetic linkage studies.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8739954

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotypic heterogeneity in the syndromes of 3-methylglutaconic aciduria

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8739954

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8739954

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/BF01799418

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8739954

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8739954%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

PubMed publication ID

8739954

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8739954

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8739954%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

 

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