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12. Long-chain fatty acid oxidation during early human development. Oey NA; den Boer ME; Wijburg FA; Vekemans M; Augé J; Steiner C; Wanders RJ; Waterham HR; Ruiter JP; Attié-Bitach T Pediatr Res; 2005 Jun; 57(6):755-9. PubMed ID: 15845636 [TBL] [Abstract][Full Text] [Related]
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14. Elevated hydroxyacylcarnitines in a carrier of LCHAD deficiency during acute liver disease of pregnancy - a common feature of the pregnancy complication? Eskelin PM; Laitinen KA; Tyni TA Mol Genet Metab; 2010 Jun; 100(2):204-6. PubMed ID: 20363656 [TBL] [Abstract][Full Text] [Related]
15. 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. den Boer ME; Ijlst L; Wijburg FA; Oostheim W; van Werkhoven MA; van Pampus MG; Heymans HS; Wanders RJ Pediatr Res; 2000 Aug; 48(2):151-4. PubMed ID: 10926288 [TBL] [Abstract][Full Text] [Related]
16. [LCHAD (long-chain 3-hydroxyacyl-CoA dehydrogenase) deficiency as a cause of sudden death of a three months old infant]. Neuman-Łaniec M; Wierzba J; Irga N; Zaborowska-Sołtys M; Balcerska A Med Wieku Rozwoj; 2002; 6(3):221-6. PubMed ID: 12637776 [TBL] [Abstract][Full Text] [Related]
17. Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency--diagnosis, plasma carnitine fractions and management in a further patient. Moore R; Glasgow JF; Bingham MA; Dodge JA; Pollitt RJ; Olpin SE; Middleton B; Carpenter K Eur J Pediatr; 1993 May; 152(5):433-6. PubMed ID: 8319713 [TBL] [Abstract][Full Text] [Related]
18. Acute fatty liver of pregnancy and long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency. Treem WR; Rinaldo P; Hale DE; Stanley CA; Millington DS; Hyams JS; Jackson S; Turnbull DM Hepatology; 1994 Feb; 19(2):339-45. PubMed ID: 8294091 [TBL] [Abstract][Full Text] [Related]
19. Maternal acute fatty liver of pregnancy associated with fetal trifunctional protein deficiency: molecular characterization of a novel maternal mutant allele. Isaacs JD; Sims HF; Powell CK; Bennett MJ; Hale DE; Treem WR; Strauss AW Pediatr Res; 1996 Sep; 40(3):393-8. PubMed ID: 8865274 [TBL] [Abstract][Full Text] [Related]
20. Urgent metabolic service improves survival in long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency detected by symptomatic identification and pilot newborn screening. Sykut-Cegielska J; Gradowska W; Piekutowska-Abramczuk D; Andresen BS; Olsen RK; Ołtarzewski M; Pronicki M; Pajdowska M; Bogdańska A; Jabłońska E; Radomyska B; Kuśmierska K; Krajewska-Walasek M; Gregersen N; Pronicka E J Inherit Metab Dis; 2011 Feb; 34(1):185-95. PubMed ID: 21103935 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]