BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

263 related articles for article (PubMed ID: 15533621)

  • 1. Maternal heterozygosity for a mitochondrial trifunctional protein mutation as a cause for liver disease in pregnancy.
    Blish KR; Ibdah JA
    Med Hypotheses; 2005; 64(1):96-100. PubMed ID: 15533621
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prospective screening for pediatric mitochondrial trifunctional protein defects in pregnancies complicated by liver disease.
    Yang Z; Yamada J; Zhao Y; Strauss AW; Ibdah JA
    JAMA; 2002 Nov; 288(17):2163-6. PubMed ID: 12413376
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant women.
    Ibdah JA; Bennett MJ; Rinaldo P; Zhao Y; Gibson B; Sims HF; Strauss AW
    N Engl J Med; 1999 Jun; 340(22):1723-31. PubMed ID: 10352164
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. [Screening for G1528C mutation in mitochondrial trifunctional protein gene in pregnant women with severe preeclampsia and new born infant].
    Wang R; Yang Z; Zhu JM; Wang JL; Yang HX; Wang Q; Zhai GR; Li Z; Yu M
    Zhonghua Fu Chan Ke Za Zhi; 2006 Oct; 41(10):672-5. PubMed ID: 17199921
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Neither maternal nor fetal mutation (E474Q) in the alpha-subunit of the trifunctional protein is frequent in pregnancies complicated by HELLP syndrome.
    Mütze S; Ahillen I; Rudnik-Schoeneborn S; Eggermann T; Leeners B; Neumaier-Wagner PM; Kuse S; Rath W; Zerres K
    J Perinat Med; 2007; 35(1):76-8. PubMed ID: 17313315
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Acute fatty liver of pregnancy, hemolysis, elevated liver enzymes, and low platelets syndrome, and long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
    Treem WR; Shoup ME; Hale DE; Bennett MJ; Rinaldo P; Millington DS; Stanley CA; Riely CA; Hyams JS
    Am J Gastroenterol; 1996 Nov; 91(11):2293-300. PubMed ID: 8931405
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Absence of the G1528C (E474Q) mutation in the alpha-subunit of the mitochondrial trifunctional protein in women with acute fatty liver of pregnancy.
    Maitra A; Domiati-Saad R; Yost N; Cunningham G; Rogers BB; Bennett MJ
    Pediatr Res; 2002 May; 51(5):658-61. PubMed ID: 11978893
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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.
    Kong XF; Zhang XX; Yu YY; Shi Q; La DD; Zhu-Ge CD; Deng L; Gong QM; Shen BY; Peng CH; Li HW
    J Gastroenterol Hepatol; 2007 Dec; 22(12):2107-11. PubMed ID: 18031367
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Acute fatty liver in pregnancy: revealing fetal fatty acid oxidation disorders].
    Lamireau D; Feghali H; Redonnet-Vernhet I; Mesli S; Carles D; Brissaud O
    Arch Pediatr; 2012 Mar; 19(3):277-81. PubMed ID: 22325456
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy.
    Sims HF; Brackett JC; Powell CK; Treem WR; Hale DE; Bennett MJ; Gibson B; Shapiro S; Strauss AW
    Proc Natl Acad Sci U S A; 1995 Jan; 92(3):841-5. PubMed ID: 7846063
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Liver disease in pregnancy and fetal fatty acid oxidation defects.
    Ibdah JA; Yang Z; Bennett MJ
    Mol Genet Metab; 2000; 71(1-2):182-9. PubMed ID: 11001809
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutations in long-chain 3-hydroxyacyl coenzyme a dehydrogenase are associated with placental maternal floor infarction/massive perivillous fibrin deposition.
    Griffin AC; Strauss AW; Bennett MJ; Ernst LM
    Pediatr Dev Pathol; 2012; 15(5):368-74. PubMed ID: 22746996
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Common missense mutation G1528C in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. Characterization and expression of the mutant protein, mutation analysis on genomic DNA and chromosomal localization of the mitochondrial trifunctional protein alpha subunit gene.
    IJlst L; Ruiter JP; Hoovers JM; Jakobs ME; Wanders RJ
    J Clin Invest; 1996 Aug; 98(4):1028-33. PubMed ID: 8770876
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Fetal fatty acid oxidation defects and maternal liver disease in pregnancy.
    Browning MF; Levy HL; Wilkins-Haug LE; Larson C; Shih VE
    Obstet Gynecol; 2006 Jan; 107(1):115-20. PubMed ID: 16394048
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Trifunctional protein deficiency: three families with significant maternal hepatic dysfunction in pregnancy not associated with E474Q mutation.
    Chakrapani A; Olpin S; Cleary M; Walter JH; Wraith JE; Besley GT
    J Inherit Metab Dis; 2000 Dec; 23(8):826-34. PubMed ID: 11196108
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Inherited long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and a fetal-maternal interaction cause maternal liver disease and other pregnancy complications.
    Strauss AW; Bennett MJ; Rinaldo P; Sims HF; O'Brien LK; Zhao Y; Gibson B; Ibdah J
    Semin Perinatol; 1999 Apr; 23(2):100-12. PubMed ID: 10331463
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.