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Volumn 168, Issue 1, 2009, Pages 103-106

Acute fatty liver of pregnancy and neonatal long-chain 3-hydroxyacyl- coenzyme a dehydrogenase (LCHAD) deficiency

Author keywords

Acute fatty liver of pregnancy; Fatty acid oxidation disorders; HELLP syndrome; LCHAD deficiency

Indexed keywords

3 HYDROXYACYL COENZYME A DEHYDROGENASE; BICARBONATE; DICARBOXYLIC ACID; GLUCOSE; LONG CHAIN TRIACYLGLYCEROL; MEDIUM CHAIN TRIACYLGLYCEROL; MITOCHONDRIAL PROTEIN;

EID: 57049166575     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00431-008-0696-z     Document Type: Article
Times cited : (16)

References (12)
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    • Heterozygosity for the common LCHAD mutation (1528G>C) is not a major cause of HELLP syndrome and the prevalence of the mutation in the Dutch population is low
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    • ME den Boer L Ijlst FA Wijburg W Oostheim MA van Werkhoven MG van Pampus HS Heymans RJ Wanders 2000 Heterozygosity for the common LCHAD mutation (1528G>C) is not a major cause of HELLP syndrome and the prevalence of the mutation in the Dutch population is low Pediatr Res 48 2 151 154
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    • Den Boer, M.E.1    Ijlst, L.2    Wijburg, F.A.3    Oostheim, W.4    Van Werkhoven, M.A.5    Van Pampus, M.G.6    Heymans, H.S.7    Wanders, R.J.8
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.