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Items: 1 to 20 of 48

1.

Liver disease in pregnancy and fetal fatty acid oxidation defects.

Ibdah JA, Yang Z, Bennett MJ.

Mol Genet Metab. 2000 Sep-Oct;71(1-2):182-9. Review.

PMID:
11001809
2.

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. Review.

PMID:
10331463
3.

Long-chain L-3-hydroxyacyl-coenzyme a dehydrogenase deficiency: a molecular and biochemical review.

Rakheja D, Bennett MJ, Rogers BB.

Lab Invest. 2002 Jul;82(7):815-24. Review.

PMID:
12118083
4.

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

Tyni T, Pihko H.

Acta Paediatr. 1999 Mar;88(3):237-45. Review.

PMID:
10229030
5.

Mitochondrial fatty acid oxidation and acute fatty liver of pregnancy.

Treem WR.

Semin Gastrointest Dis. 2002 Jan;13(1):55-66. Review.

PMID:
11944635
6.

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. Review.

PMID:
11978893
7.

Acute fatty liver of pregnancy: an update on pathogenesis and clinical implications.

Ibdah JA.

World J Gastroenterol. 2006 Dec 14;12(46):7397-404. Review.

8.

Fatty acid transport and mitochondrial oxidation disorders.

Rinaldo P.

Semin Liver Dis. 2001 Nov;21(4):489-500. Review.

PMID:
11745037
9.
10.

Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship.

Gregersen N, Andresen BS, Corydon MJ, Corydon TJ, Olsen RK, Bolund L, Bross P.

Hum Mutat. 2001 Sep;18(3):169-89. Review.

PMID:
11524729
11.

An overview of beta-oxidation disorders.

Moczulski D, Majak I, Mamczur D.

Postepy Hig Med Dosw (Online). 2009 Jun 8;63:266-77. Review.

12.

Peroxisomal beta-oxidation and steatohepatitis.

Rao MS, Reddy JK.

Semin Liver Dis. 2001;21(1):43-55. Review.

PMID:
11296696
13.

Mitochondrial fatty acid oxidation disorders: pathophysiological studies in mouse models.

Spiekerkoetter U, Wood PA.

J Inherit Metab Dis. 2010 Oct;33(5):539-46. doi: 10.1007/s10545-010-9121-7. Epub 2010 Jun 8. Review.

14.

[Pregnancy and inborn errors of metabolism].

Radomyska B.

Ginekol Pol. 2003 Jun;74(6):479-85. Review. Polish.

PMID:
12931456
15.

Imitators of severe preeclampsia.

Sibai BM.

Obstet Gynecol. 2007 Apr;109(4):956-66. Review.

PMID:
17400860
16.
17.

[HELLP syndrome. Critical state. Current concepts].

Rojas Poceros G, Viveros-Renteria E, Kably-Ambe A.

Ginecol Obstet Mex. 1996 Feb;64:64-72. Review. Spanish.

PMID:
8714066
18.

Acute fatty liver of pregnancy.

Simpson KR, Luppi CJ, O'Brien-Abel N.

J Perinat Neonatal Nurs. 1998 Mar;11(4):35-44. Review.

PMID:
9592460
19.

Short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with hyperinsulinism: a novel glucose-fatty acid cycle?

Eaton S, Chatziandreou I, Krywawych S, Pen S, Clayton PT, Hussain K.

Biochem Soc Trans. 2003 Dec;31(Pt 6):1137-9. Review.

PMID:
14641012
20.

Corticosteroids, pregnancy, and HELLP syndrome: a review.

van Runnard Heimel PJ, Franx A, Schobben AF, Huisjes AJ, Derks JB, Bruinse HW.

Obstet Gynecol Surv. 2005 Jan;60(1):57-70; quiz 73-4. Review.

PMID:
15618920

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