(Q46958578)

English

Carnitine membrane transporter deficiency: a rare treatable cause of cardiomyopathy and anemia

scientific article published on 10 October 2007

In more languages

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17926086

Carnitine membrane transporter deficiency: a rare treatable cause of cardiomyopathy and anemia (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17926086

1 reference

based on heuristic

inferred from title

author name string

Aline Cano

1

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17926086

Caroline Ovaert

2

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17926086

Christine Vianey-Saban

3

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17926086

Brigitte Chabrol

4

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17926086

publication date

10 October 2007

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17926086

Pediatric Cardiology

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17926086

29

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17926086

1

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17926086

163-165

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17926086

https://scigraph.springernature.com/pub.10.1007/s00246-007-9051-9

0 references

Disorders of carnitine transport and the carnitine cycle

1 reference

https://api.crossref.org/works/10.1007%2FS00246-007-9051-9

21 January 2018

Carnitine transport: pathophysiology and metabolism of known molecular defects

1 reference

https://pubmed.ncbi.nlm.nih.gov/17926086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Serum free carnitine and total triglycerid levels in children with iron deficiency anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/17926086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carnitine metabolism and deficit--when supplementation is necessary?

1 reference

https://pubmed.ncbi.nlm.nih.gov/17926086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter

1 reference

https://pubmed.ncbi.nlm.nih.gov/17926086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Low serum carnitine concentrations in healthy children with iron deficiency anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/17926086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary carnitine deficiency due to a failure of carnitine transport in kidney, muscle, and fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/17926086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic epidemiology of the carnitine transporter OCTN2 gene in a Japanese population and phenotypic characterization in Japanese pedigrees with primary systemic carnitine deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/17926086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00246-007-9051-9

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17926086

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17926086

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