Inherited long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and a fetal-maternal interaction cause maternal liver disease and other pregnancy complications.
about
Fetal fatty acid oxidation disorders, their effect on maternal health and neonatal outcome: impact of expanded newborn screening on their diagnosis and managementGlutamate 170 of human l-3-hydroxyacyl-CoA dehydrogenase is required for proper orientation of the catalytic histidine and structural integrity of the enzymeAcute Fatty Liver Disease of Pregnancy: Updates in Pathogenesis, Diagnosis, and Management.Inborn errors of mitochondrial fatty acid oxidation.Short-chain acyl-CoA dehydrogenase (SCAD) deficiency: an examination of the medical and neurodevelopmental characteristics of 14 cases identified through newborn screening or clinical symptomsAbsence of the G1528C (E474Q) mutation in the alpha-subunit of the mitochondrial trifunctional protein in women with acute fatty liver of pregnancy.Clinical outcome, biochemical and therapeutic follow-up in 14 Austrian patients with Long-Chain 3-Hydroxy Acyl CoA Dehydrogenase Deficiency (LCHADD).Gestational Diabetes Associated with a Novel Mutation (378-379insTT) in the Glycerol Kinase Gene.Pregnancy in women with inherited metabolic disease.Identification of a novel single nucleotide polymorphism of HADHA gene at a referred primer-binding site during pre-diagnostic tests for preimplantation genetic diagnosis.Current concepts of mechanisms in drug-induced hepatotoxicity.Management of an LCHADD Patient During Pregnancy and High Intensity Exercise.Preeclampsia and HELLP syndrome: impaired mitochondrial function in umbilical endothelial cells.No mutation was found in the alpha-subunit of the mitochondrial tri-functional protein in one patient with severe acute fatty liver of pregnancy and her relatives.The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation.Guidelines for the use of antiretroviral agents in HIV-infected adults and adolescents. February 5, 2001.
P2860
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P2860
Inherited long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and a fetal-maternal interaction cause maternal liver disease and other pregnancy complications.
description
1999 nî lūn-bûn
@nan
1999 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Inherited long-chain 3-hydroxy ...... other pregnancy complications.
@ast
Inherited long-chain 3-hydroxy ...... other pregnancy complications.
@en
type
label
Inherited long-chain 3-hydroxy ...... other pregnancy complications.
@ast
Inherited long-chain 3-hydroxy ...... other pregnancy complications.
@en
prefLabel
Inherited long-chain 3-hydroxy ...... other pregnancy complications.
@ast
Inherited long-chain 3-hydroxy ...... other pregnancy complications.
@en
P2093
P1476
Inherited long-chain 3-hydroxy ...... other pregnancy complications.
@en
P2093
Bennett MJ
O'Brien LK
Strauss AW
P304
P356
10.1016/S0146-0005(99)80044-5
P577
1999-04-01T00:00:00Z