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Volumn 168, Issue 1, 2009, Pages 103-106
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Acute fatty liver of pregnancy and neonatal long-chain 3-hydroxyacyl- coenzyme a dehydrogenase (LCHAD) deficiency
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Author keywords
Acute fatty liver of pregnancy; Fatty acid oxidation disorders; HELLP syndrome; LCHAD deficiency
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Indexed keywords
3 HYDROXYACYL COENZYME A DEHYDROGENASE;
BICARBONATE;
DICARBOXYLIC ACID;
GLUCOSE;
LONG CHAIN TRIACYLGLYCEROL;
MEDIUM CHAIN TRIACYLGLYCEROL;
MITOCHONDRIAL PROTEIN;
ACUTE DISEASE;
ACUTE FATTY LIVER OF PREGNANCY;
ALLELE;
ARTICLE;
BLOOD CLOTTING DISORDER;
BLOOD TRANSFUSION;
CASE REPORT;
CAUSE OF DEATH;
DIET RESTRICTION;
DIET THERAPY;
ECHOCARDIOGRAPHY;
ENZYME ACTIVITY;
ENZYME DEFICIENCY;
FAMILY HISTORY;
FATTY ACID OXIDATION;
FATTY LIVER;
FEMALE;
FETUS MOVEMENT;
FOLLOW UP;
GENETIC ANALYSIS;
GESTATIONAL AGE;
HEPATOMEGALY;
HOMOZYGOSITY;
HUMAN;
HYPERAMMONEMIA;
HYPERTROPHIC CARDIOMYOPATHY;
HYPOGLYCEMIA;
INFANT;
LACTIC ACIDOSIS;
LIVER FUNCTION TEST;
LONG CHAIN 3 HYDROXYACYL COENZYME A DEHYDROGENASE DEFICIENCY;
MATERNAL WELFARE;
METABOLIC DISORDER;
MISSENSE MUTATION;
NASOGASTRIC TUBE;
NEWBORN DISEASE;
NEWBORN SCREENING;
OPHTHALMOSCOPY;
PERCUTANEOUS ENDOSCOPIC GASTROSTOMY;
PREGNANCY;
PREGNANCY COMPLICATION;
PRIORITY JOURNAL;
RETINOPATHY;
STOMACH TUBE;
3-HYDROXYACYL COA DEHYDROGENASES;
ACUTE DISEASE;
ALLELES;
BLOOD TRANSFUSION;
CARDIOMYOPATHIES;
FATTY LIVER;
FEMALE;
GENE EXPRESSION;
HUMANS;
INFANT;
METABOLISM, INBORN ERRORS;
PREGNANCY;
PREGNANCY COMPLICATIONS;
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EID: 57049166575
PISSN: 03406199
EISSN: None
Source Type: Journal
DOI: 10.1007/s00431-008-0696-z Document Type: Article |
Times cited : (16)
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References (12)
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