(Q34141683)

31 July 2017

1 reference

title

Prenatal diagnosis of disorders of fatty acid transport and mitochondrial oxidation (English)

1 reference

31 July 2017

0 references

Rinaldo P

1

1 reference

PubMed ID

11180241

31 July 2017

Studinski AL

series ordinal

2

1 reference

PubMed ID

11180241

31 July 2017

Matern D

series ordinal

3

1 reference

31 July 2017

1 January 2001

1 reference

31 July 2017

1 reference

31 July 2017

21

1 reference

31 July 2017

52-54

1 reference

31 July 2017

1

1 reference

Inborn errors of mitochondrial fatty acid oxidation

31 July 2017

1 reference

https://api.crossref.org/works/10.1002%2F1097-0223%28200101%2921%3A1%3C52%3A%3AAID-PD973%3E3.0.CO%3B2-H

Carnitine palmitoyltransferase deficiencies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0223%28200101%2921%3A1%3C52%3A%3AAID-PD973%3E3.0.CO%3B2-H

Mitochondrial carnitine-acylcarnitine translocase deficiency presenting as sudden neonatal death.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0223%28200101%2921%3A1%3C52%3A%3AAID-PD973%3E3.0.CO%3B2-H

A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant women

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0223%28200101%2921%3A1%3C52%3A%3AAID-PD973%3E3.0.CO%3B2-H

Sudden neonatal death in carnitine transporter deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0223%28200101%2921%3A1%3C52%3A%3AAID-PD973%3E3.0.CO%3B2-H

Recent developments in the investigation of inherited metabolic disorders using cultured human cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0223%28200101%2921%3A1%3C52%3A%3AAID-PD973%3E3.0.CO%3B2-H

Prenatal diagnosis of organic acidemias based on amniotic fluid levels of acylcarnitines

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0223%28200101%2921%3A1%3C52%3A%3AAID-PD973%3E3.0.CO%3B2-H

Mitochondrial very-long-chain acyl-coenzyme A dehydrogenase deficiency: clinical characteristics and diagnostic considerations in 30 patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0223%28200101%2921%3A1%3C52%3A%3AAID-PD973%3E3.0.CO%3B2-H

Disorders of mitochondrial fatty acyl-CoA beta-oxidation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0223%28200101%2921%3A1%3C52%3A%3AAID-PD973%3E3.0.CO%3B2-H

Prenatal Diagnosis and Neonatal Monitoring of a Fetus with Glutaric Aciduria Type II Due to Electron Transfer Flavoprotein (β-Subunit) Deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0223%28200101%2921%3A1%3C52%3A%3AAID-PD973%3E3.0.CO%3B2-H

DNA-based prenatal diagnosis for very-long-chain acyl-CoA dehydrogenase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0223%28200101%2921%3A1%3C52%3A%3AAID-PD973%3E3.0.CO%3B2-H

Prenatal diagnosis of medium-chain acyl-coenzyme A dehydrogenase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0223%28200101%2921%3A1%3C52%3A%3AAID-PD973%3E3.0.CO%3B2-H

Prenatal diagnosis of mitochondrial fatty acid oxidation defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0223%28200101%2921%3A1%3C52%3A%3AAID-PD973%3E3.0.CO%3B2-H

The HELLP syndrome associated wiht fetal medium-chain acyl-CoA dehydrogenase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0223%28200101%2921%3A1%3C52%3A%3AAID-PD973%3E3.0.CO%3B2-H

Acylcarnitines in fibroblasts of patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and other fatty acid oxidation disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1097-0223%28200101%2921%3A1%3C52%3A%3AAID-PD973%3E3.0.CO%3B2-H

10.1002/1097-0223(200101)21:1<52::AID-PD973>3.0.CO;2-H

21 January 2018

Identifiers

DOI

1 reference

31 July 2017

1 reference

PubMed ID

11180241