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Results: 1 to 20 of 21

Related Articles by Review for PubMed (Select 7811722)

1.
2.

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
3.

The clinical spectrum of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

Pons R, Roig M, Riudor E, Ribes A, Briones P, Ortigosa L, Baldellou A, Gil-Gibernau J, Olesti M, Navarro C, Wanders RJ.

Pediatr Neurol. 1996 Apr;14(3):236-43. Review.

PMID:
8736409
4.

Molecular diagnosis and characterization of medium-chain acyl-CoA dehydrogenase deficiency.

Andresen BS, Bross P, Jensen TG, Knudsen I, Winter V, Kølvraa S, Bolund L, Gregersen N.

Scand J Clin Lab Invest Suppl. 1995;220:9-25. Review.

PMID:
7652482
5.

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

Tyni T, Pihko H.

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

PMID:
10229030
6.

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
7.
8.

Mouse models for disorders of mitochondrial fatty acid beta-oxidation.

Schuler AM, Wood PA.

ILAR J. 2002;43(2):57-65. Review.

9.

[Long-chain-3-hydroxyacyl-CoA dehydrogenase deficiency].

Uchiyama A, Yamaguchi S.

Nihon Rinsho. 2002 Apr;60 Suppl 4:730-3. Review. Japanese. No abstract available.

PMID:
12013985
11.

[Short chain 3-hydroxyacyl-CoA dehydrogenase deficiency].

Kimura M, Yamaguchi S.

Nihon Rinsho. 2002 Apr;60 Suppl 4:734-7. Review. Japanese. No abstract available.

PMID:
12013986
12.

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
13.

The mitochondrial long-chain trifunctional enzyme: 2-enoyl-CoA hydratase, 3-hydroxyacyl-CoA dehydrogenase and 3-oxoacyl-CoA thiolase.

Middleton B.

Biochem Soc Trans. 1994 May;22(2):427-31. Review. No abstract available.

PMID:
7958339
14.

The mitochondrial trifunctional protein: centre of a beta-oxidation metabolon?

Eaton S, Bursby T, Middleton B, Pourfarzam M, Mills K, Johnson AW, Bartlett K.

Biochem Soc Trans. 2000 Feb;28(2):177-82. Review.

PMID:
10816122
15.

Novel insights into fatty acid oxidation, amino acid metabolism, and insulin secretion from studying patients with loss of function mutations in 3-hydroxyacyl-CoA dehydrogenase.

Heslegrave AJ, Hussain K.

J Clin Endocrinol Metab. 2013 Feb;98(2):496-501. doi: 10.1210/jc.2012-3134. Epub 2012 Dec 18. Review.

PMID:
23253615
16.

[Mitochondrial 3-hydroxyacyl-CoA dehydrogenase (SCHAD, LCHAD)].

Yamaguchi S.

Nihon Rinsho. 2002 Apr;60 Suppl 4:101-4. Review. Japanese. No abstract available.

PMID:
12013827
17.

Observations regarding retinopathy in mitochondrial trifunctional protein deficiencies.

Fletcher AL, Pennesi ME, Harding CO, Weleber RG, Gillingham MB.

Mol Genet Metab. 2012 May;106(1):18-24. doi: 10.1016/j.ymgme.2012.02.015. Epub 2012 Mar 8. Review.

18.

[Trifunctional protein deficiency and long-chain-3-hydroxy-acyl CoA dehydrogenase deficiency].

Kimura M, Yamaguchi S.

Ryoikibetsu Shokogun Shirizu. 2001;(36):77-9. Review. Japanese. No abstract available.

PMID:
11596456
19.

Hydroxysteroid (17β) dehydrogenase X in human health and disease.

Yang SY, He XY, Miller D.

Mol Cell Endocrinol. 2011 Aug 22;343(1-2):1-6. doi: 10.1016/j.mce.2011.06.011. Epub 2011 Jun 25. Review.

PMID:
21708223
20.

The short-chain alcohol dehydrogenase superfamily: variations on a common theme.

Krozowski Z.

J Steroid Biochem Mol Biol. 1994 Nov;51(3-4):125-30. Review.

PMID:
7981120
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