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3-hydroxyacyl-CoA dehydrogenase (HAD) deficiency replaces short-chain hydroxyacyl-CoA dehydrogenase (SCHAD) deficiency as well as medium- and short-chain hydroxyacyl-CoA dehydrogenase (M/SCHAD) deficiency as the consensus name of this fatty acid oxidation disorder.

作者信息

He Xue-Ying, Yang Song-Yu

出版信息

Mol Genet Metab. 2007 Jun;91(2):205-6. doi: 10.1016/j.ymgme.2007.02.015. Epub 2007 Apr 16.

DOI:10.1016/j.ymgme.2007.02.015
PMID:17434778
Abstract
摘要

相似文献

1
3-hydroxyacyl-CoA dehydrogenase (HAD) deficiency replaces short-chain hydroxyacyl-CoA dehydrogenase (SCHAD) deficiency as well as medium- and short-chain hydroxyacyl-CoA dehydrogenase (M/SCHAD) deficiency as the consensus name of this fatty acid oxidation disorder.
Mol Genet Metab. 2007 Jun;91(2):205-6. doi: 10.1016/j.ymgme.2007.02.015. Epub 2007 Apr 16.
2
3-Hydroxyacyl-CoA dehydrogenase and short chain 3-hydroxyacyl-CoA dehydrogenase in human health and disease.3-羟基酰基辅酶A脱氢酶和短链3-羟基酰基辅酶A脱氢酶与人类健康和疾病
FEBS J. 2005 Oct;272(19):4874-83. doi: 10.1111/j.1742-4658.2005.04911.x.
3
Mitochondrial fatty acid beta-oxidation in the human eye and brain: implications for the retinopathy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.人眼和大脑中的线粒体脂肪酸β-氧化：对长链3-羟基酰基辅酶A脱氢酶缺乏症视网膜病变的影响。
Pediatr Res. 2004 Nov;56(5):744-50. doi: 10.1203/01.PDR.0000141967.52759.83. Epub 2004 Sep 3.
4
[Short-chain 3-hydroxyacyl-CoA dehydrogenase (SCHAD) deficiency].[短链3-羟酰基辅酶A脱氢酶（SCHAD）缺乏症]
Ryoikibetsu Shokogun Shirizu. 1998(18 Pt 1):420-1.
5
[Short-chain 3-hydroxyacyl-CoA dehydrogenase (SCHAD) deficiency].
Ryoikibetsu Shokogun Shirizu. 2001(36):74-6.
6
Role of short-chain hydroxyacyl CoA dehydrogenases in SCHAD deficiency.短链羟酰基辅酶A脱氢酶在SCHAD缺乏症中的作用。
Biochem Biophys Res Commun. 2008 Mar 28;368(1):6-11. doi: 10.1016/j.bbrc.2007.10.188. Epub 2007 Nov 26.
7
Short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency in muscle: a new cause for recurrent myoglobinuria and encephalopathy.
Ann Neurol. 1991 Sep;30(3):415-9. doi: 10.1002/ana.410300315.
8
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.
Pediatr Res. 1991 Apr;29(4 Pt 1):406-11. doi: 10.1203/00006450-199104000-00016.
9
Reye-like syndrome resulting from novel missense mutations in mitochondrial medium- and short-chain l-3-hydroxy-acyl-CoA dehydrogenase.线粒体中链和短链L-3-羟基酰基辅酶A脱氢酶新的错义突变导致的瑞氏综合征样综合征。
Mol Genet Metab. 2006 Sep-Oct;89(1-2):74-9. doi: 10.1016/j.ymgme.2006.04.004. Epub 2006 May 24.
10
Placental floor infarction complicating the pregnancy of a fetus with long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency.
Mol Genet Metab. 2001 Mar;72(3):265-8. doi: 10.1006/mgme.2000.3135.

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Involvement of Type 10 17β-Hydroxysteroid Dehydrogenase in the Pathogenesis of Infantile Neurodegeneration and Alzheimer's Disease.10 型 17β-羟类固醇脱氢酶在婴儿神经退行性疾病和阿尔茨海默病发病机制中的作用。
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Measurement of tissue acyl-CoAs using flow-injection tandem mass spectrometry: acyl-CoA profiles in short-chain fatty acid oxidation defects.使用流动注射串联质谱法测量组织酰基辅酶 A：短链脂肪酸氧化缺陷中的酰基辅酶 A 谱。
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