(Q28214659)

https://api.crossref.org/works/10.1097/01.LAB.0000021175.50201.46

Structural analysis of cDNAs for subunits of human mitochondrial fatty acid beta-oxidation trifunctional protein

20 April 2017

1 reference

https://api.crossref.org/works/10.1097/01.LAB.0000021175.50201.46

Fatty acid import into mitochondria

20 April 2017

1 reference

https://api.crossref.org/works/10.1097/01.LAB.0000021175.50201.46

Genomic and mutational analysis of the mitochondrial trifunctional protein beta-subunit (HADHB) gene in patients with trifunctional protein deficiency

20 April 2017

1 reference

https://api.crossref.org/works/10.1097/01.LAB.0000021175.50201.46

Acute fatty liver of pregnancy

20 April 2017

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Inborn errors of mitochondrial fatty acid oxidation

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Mitochondrial short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency: a new defect of fatty acid oxidation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Two alpha subunit donor splice site mutations cause human trifunctional protein deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Human liver long-chain 3-hydroxyacyl-coenzyme A dehydrogenase is a multifunctional membrane-bound beta-oxidation enzyme of mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Secondary respiratory chain defect in a boy with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: possible diagnostic pitfalls

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

The pathogenesis of pre-eclampsia: new aspects

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Hyperemesis gravidarum: a current review

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Dietary management of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD). A case report and survey

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Lipid-mediated endothelial dysfunction: a common factor to preeclampsia and chronic vascular disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Docosahexaenoic acid and retinal function in children with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Heterozygosity for long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency and deterioration in liver function in a newborn infant infected with human immunodeficiency virus

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

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/10.1097%2F01.LAB.0000021175.50201.46

Mild trifunctional protein deficiency is associated with progressive neuropathy and myopathy and suggests a novel genotype-phenotype correlation

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Molecular prenatal diagnosis in families with fetal mitochondrial trifunctional protein mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

A successful strategy for preimplantation diagnosis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Maternal acute fatty liver of pregnancy associated with fetal trifunctional protein deficiency: molecular characterization of a novel maternal mutant allele

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

First trimester prenatal diagnosis: chorionic villus sampling

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Pigmentary retinopathy in long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

The mitochondrial carnitine palmitoyltransferase system. From concept to molecular analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Mitochondrial trifunctional protein deficiency associated with recurrent myoglobinuria in adolescence.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Differential regulation in the heart of mitochondrial carnitine palmitoyltransferase-I muscle and liver isoforms

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

First trimester prenatal diagnosis: fetal cells in the maternal circulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Disorders of mitochondrial long-chain fatty acid oxidation

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

The clinical spectrum of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Evidence that the sensitivity of carnitine palmitoyltransferase I to inhibition by malonyl-CoA is an important site of regulation of hepatic fatty acid oxidation in the fetal and newborn rabbit. Perinatal development and effects of pancreatic hormon

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Pathogenesis and genetics of pre-eclampsia

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Deficiency of long-chain 3-hydroxyacyl-CoA dehydrogenase: a cause of lethal myopathy and cardiomyopathy in early childhood

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Regulation of mitochondrial carnitine palmitoyl transferases from liver and extrahepatic tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Retinal dystrophy in long chain 3-hydroxy-acyl-coA dehydrogenase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: a severe fatty acid oxidation disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Ultrastructural aspects of preeclampsia. II. Mitochondrial changes

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Ophthalmologic findings in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation: a new type of hereditary metabolic chorioretinopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency with the G1528C mutation: clinical presentation of thirteen patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Maternal floor infarction: relationship to X cells, major basic protein, and adverse perinatal outcome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid beta-oxidation

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Disorders of mitochondrial fatty acyl-CoA beta-oxidation

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Placental mitochondria as a source of oxidative stress in pre-eclampsia

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Strategies for preimplantation genetic diagnosis of single gene disorders by DNA amplification.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Effect of fatty acids on energy coupling processes in mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Peripheral sensory-motor polyneuropathy, pigmentary retinopathy, and fatal cardiomyopathy in long-chain 3-hydroxy-acyl-CoA dehydrogenase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46

Hypoparathyroidism in mitochondrial trifunctional protein deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.LAB.0000021175.50201.46