(Q33637030)

English

Inherited long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and a fetal-maternal interaction cause maternal liver disease and other pregnancy complications

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scholarly article

1 reference

Europe PubMed Central

28 July 2017

1 reference

Europe PubMed Central

Inherited long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and a fetal-maternal interaction cause maternal liver disease and other pregnancy complications (English)

1 reference

Europe PubMed Central

28 July 2017

maternal health

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inferred from title

long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

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author name string

Strauss AW

1

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Europe PubMed Central

28 July 2017

Bennett MJ

2

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Europe PubMed Central

28 July 2017

Rinaldo P

3

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Europe PubMed Central

28 July 2017

Sims HF

4

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Europe PubMed Central

28 July 2017

O'Brien LK

5

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Europe PubMed Central

28 July 2017

Zhao Y

6

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Europe PubMed Central

28 July 2017

Gibson B

7

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Europe PubMed Central

28 July 2017

Ibdah J

8

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Europe PubMed Central

28 July 2017

publication date

1 April 1999

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Europe PubMed Central

28 July 2017

Seminars in Perinatology

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Europe PubMed Central

28 July 2017

23

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Europe PubMed Central

28 July 2017

100-112

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Europe PubMed Central

28 July 2017

2

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Europe PubMed Central

28 July 2017

Liver disease in pregnancy

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Hepatic disease in pregnancy

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7 January 2021

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Idiopathic fatty liver of pregnancy: findings in ten cases

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Maternal morbidity and mortality in 442 pregnancies with hemolysis, elevated liver enzymes, and low platelets (HELLP syndrome)

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Preeclampsia: a microvesicular fat disease of the liver?

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Fatty acid oxidation disorders: A new class of metabolic diseases

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Mammalian mitochondrial beta-oxidation

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Disorders of mitochondrial long-chain fatty acid oxidation

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

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Molecular basis of human mitochondrial very-long-chain acyl-CoA dehydrogenase deficiency causing cardiomyopathy and sudden death in childhood

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Molecular characterization of inherited medium-chain acyl-CoA dehydrogenase deficiency

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A novel mutation in medium chain acyl-CoA dehydrogenase causes sudden neonatal death

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Molecular basis of hepatic carnitine palmitoyltransferase I deficiency

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The human medium chain Acyl-CoA dehydrogenase gene promoter consists of a complex arrangement of nuclear receptor response elements and Sp1 binding sites

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Mitochondrial trifunctional protein deficiency. Catalytic heterogeneity of the mutant enzyme in two patients

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

1 reference

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7 January 2021

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Medium-chain acyl-CoA dehydrogenase deficiency. Diagnosis by stable-isotope dilution measurement of urinary n-hexanoylglycine and 3-phenylpropionylglycine

1 reference

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

1 reference

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3-Hydroxyoctanoic aciduria: identification of a new organic acid in the urine of a patient with non-ketotic hypoglycemia

1 reference

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

1 reference

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7 January 2021

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Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

1 reference

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7 January 2021

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Human trifunctional protein deficiency: A new disorder of mitochondrial fatty acid β-oridation

1 reference

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7 January 2021

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Combined enzyme defect of mitochondrial fatty acid oxidation

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

1 reference

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Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of the major disease-causing mutation in the alpha-subunit of the mitochondrial trifunctional protein

1 reference

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

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980044-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980044-5

7 January 2021

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1 reference

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

1 reference

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Clinical and biochemical presentation of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

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7 January 2021

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Pregnancy complications are frequent in long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

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7 January 2021

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Two mitochondrial 3-hydroxyacyl-CoA dehydrogenases in bovine liver

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Nonsense mutations inhibit RNA splicing in a cell-free system: recognition of mutant codon is independent of protein synthesis

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Mammalian orthologues of a yeast regulator of nonsense transcript stability

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

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

1 reference

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Pregnancy and fetal long-chain 3-hydroxyacyl coenzyme A dehydrogenase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980044-5

7 January 2021

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Syndrome of hemolysis, elevated liver enzymes, and low platelet count: a severe consequence of hypertension in pregnancy

1 reference

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Acute fatty liver of pregnancy: a clinical study of 12 episodes in 11 patients

1 reference

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Recurrent acute fatty liver of pregnancy associated with a fatty-acid oxidation defect in the offspring

1 reference

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Assessment of the prevalence of genetic metabolic defects in acute fatty liver of pregnancy

1 reference

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Decreased mitochondrial oxidation of fatty acids in pregnant mice: possible relevance to development of acute fatty liver of pregnancy

1 reference

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Identifiers

10.1016/S0146-0005(99)80044-5

1 reference

Europe PubMed Central

28 July 2017

1 reference

Europe PubMed Central

28 July 2017

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