(Q48449238)

11 February 2018

title

A survey of Japanese patients with mitochondrial fatty acid beta-oxidation and related disorders as detected from 1985 to 2000. (English)

1 reference

11 February 2018

0 references

2

1 reference

11 February 2018

author name string

Yoshiko Tamaoki

1

1 reference

11 February 2018

Yuki Hasegawa

3

1 reference

11 February 2018

Misako Iga

4

1 reference

11 February 2018

Makoto Inoue

5

1 reference

11 February 2018

Seiji Yamaguchi

6

1 reference

11 February 2018

publication date

1 October 2002

1 reference

11 February 2018

published in

Brain and Development

1 reference

11 February 2018

volume

24

1 reference

11 February 2018

issue

7

1 reference

11 February 2018

page(s)

675-680

1 reference

11 February 2018

Inborn errors of mitochondrial fatty acid oxidation

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2802%2900074-8

7 January 2021

Disorders of mitochondrial fatty acyl-CoA beta-oxidation

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2802%2900074-8

7 January 2021

Defects in activation and transport of fatty acids

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2802%2900074-8

7 January 2021

Recognition of medium-chain acyl-CoA dehydrogenase deficiency in asymptomatic siblings of children dying of sudden infant death or Reye-like syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2802%2900074-8

7 January 2021

Medium-chain acyl-coenzyme A dehydrogenase deficiency and sudden infant death

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2802%2900074-8

7 January 2021

Arrhythmias and conduction defects as presenting symptoms of fatty acid oxidation disorders in children

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2802%2900074-8

7 January 2021

New developments in the pathophysiology, clinical spectrum, and diagnosis of disorders of fatty acid oxidation

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2802%2900074-8

7 January 2021

Identification of a common mutation in patients with medium-chain acyl-CoA dehydrogenase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2802%2900074-8

7 January 2021

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://api.crossref.org/works/10.1016%2FS0387-7604%2802%2900074-8

7 January 2021

Prevalence of K329E mutation in medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cards

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2802%2900074-8

7 January 2021

Very long chain acyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid oxidation in fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2802%2900074-8

7 January 2021

A novel disease with deficiency of mitochondrial very-long-chain acyl-CoA dehydrogenase

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2802%2900074-8

7 January 2021

Identification of very-long-chain acyl-CoA dehydrogenase deficiency in three patients previously diagnosed with long-chain acyl-CoA dehydrogenase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2802%2900074-8

7 January 2021

Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiency.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2802%2900074-8

7 January 2021

Recognition and management of fatty acid oxidation defects: a series of 107 patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2802%2900074-8

7 January 2021

Outcome of medium chain acyl-CoA dehydrogenase deficiency after diagnosis

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2802%2900074-8

7 January 2021

Retrospective biochemical screening of fatty acid oxidation disorders in postmortem livers of 418 cases of sudden death in the first year of life

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2802%2900074-8

7 January 2021

Sudden and unexpected neonatal death: a protocol for the postmortem diagnosis of fatty acid oxidation disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2802%2900074-8

7 January 2021

Laboratory integration and utilization of tandem mass spectrometry in neonatal screening: a model for clinical mass spectrometry in the next millennium

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2802%2900074-8

7 January 2021

10.1016/S0387-7604(02)00074-8

Identifiers

DOI

1 reference

11 February 2018

1 reference

11 February 2018