• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验

Inherited disorders of straight chain fatty acid oxidation.

作者信息

Pollitt R J

出版信息

Arch Dis Child. 1987 Jan;62(1):6-7. doi: 10.1136/adc.62.1.6.

DOI:10.1136/adc.62.1.6
PMID:3813638
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1778136/
Abstract
摘要

相似文献

1
Inherited disorders of straight chain fatty acid oxidation.直链脂肪酸氧化的遗传性疾病。
Arch Dis Child. 1987 Jan;62(1):6-7. doi: 10.1136/adc.62.1.6.
2
The diagnosis and biochemical investigation of a patient with a short chain fatty acid oxidation defect.
J Inherit Metab Dis. 1985;8 Suppl 2:135-6. doi: 10.1007/BF01811496.
3
Fatty acid oxidation disorders: a new class of metabolic diseases.脂肪酸氧化障碍：一类新型代谢疾病。
J Pediatr. 1992 Jul;121(1):1-11. doi: 10.1016/s0022-3476(05)82532-6.
4
Disorders of fatty acid oxidation.脂肪酸氧化紊乱
Handb Clin Neurol. 2013;113:1675-88. doi: 10.1016/B978-0-444-59565-2.00035-6.
5
Prenatal diagnosis of a defect in medium-chain fatty acid oxidation.
J Inherit Metab Dis. 1994;17(3):279-82. doi: 10.1007/BF00711807.
6
Improved detection of long-chain fatty acid oxidation defects in intact cells using [9,10-3H]oleic acid.使用[9,10-3H]油酸改进完整细胞中长链脂肪酸氧化缺陷的检测。
J Inherit Metab Dis. 1997 Jul;20(3):415-9. doi: 10.1023/a:1005358802096.
7
[Clinical protocols concerned with disorders of fatty acid beta oxidation].[与脂肪酸β氧化紊乱相关的临床方案]
Przegl Lek. 1994;51(1):25-8.
8
Sudden infant death syndrome and inherited disorders of fatty acid beta-oxidation.婴儿猝死综合征与脂肪酸β氧化的遗传性疾病
Biol Neonate. 1990;58 Suppl 1:70-80. doi: 10.1159/000243301.
9
Rapid diagnosis of long chain and medium chain fatty acid oxidation disorders using lymphocytes.利用淋巴细胞快速诊断长链和中链脂肪酸氧化障碍
Ann Clin Biochem. 1995 Mar;32 ( Pt 2):154-9. doi: 10.1177/000456329503200204.
10
Quantitative plasma acylcarnitine analysis using electrospray tandem mass spectrometry for the diagnosis of organic acidaemias and fatty acid oxidation defects.采用电喷雾串联质谱法进行血浆酰基肉碱定量分析以诊断有机酸血症和脂肪酸氧化缺陷。
J Inherit Metab Dis. 1999 May;22(3):302-6. doi: 10.1023/a:1005587617745.

引用本文的文献

1
Acylcoenzyme A dehydrogenase deficiency in heart tissue from infants who died unexpectedly with fatty change in the liver.意外死亡且肝脏有脂肪变性的婴儿心脏组织中的酰基辅酶A脱氢酶缺乏症
Br Med J (Clin Res Ed). 1988 Jan 2;296(6614):11-2. doi: 10.1136/bmj.296.6614.11.
2
Interrelationships of liver and brain with special reference to Reye syndrome.
J Inherit Metab Dis. 1991;14(4):436-58. doi: 10.1007/BF01797917.
3
The phenylpropionic acid load test: experience with 72 children at-risk for beta-oxidation disorders.
Ir J Med Sci. 1992 Oct;161(10):586-8. doi: 10.1007/BF02942363.

本文引用的文献

1
General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three cases.一般型（中链）酰基辅酶A脱氢酶缺乏症（非酮症性二羧酸尿症）：三例患者23种具有生物学意义的有机酸的尿排泄定量模式
Clin Chim Acta. 1983 Aug 15;132(2):181-91. doi: 10.1016/0009-8981(83)90246-2.
2
Long-chain acyl coenzyme A dehydrogenase deficiency: an inherited cause of nonketotic hypoglycemia.长链酰基辅酶A脱氢酶缺乏症：非酮症低血糖的一种遗传病因。
Pediatr Res. 1985 Jul;19(7):666-71. doi: 10.1203/00006450-198507000-00006.
3
Fluorometric assay of acyl-CoA dehydrogenases in normal and mutant human fibroblasts.
Biochem Med. 1985 Feb;33(1):38-44. doi: 10.1016/0006-2944(85)90124-3.
4
Recognition of medium-chain acyl-CoA dehydrogenase deficiency in asymptomatic siblings of children dying of sudden infant death or Reye-like syndromes.在死于婴儿猝死或类瑞氏综合征的儿童无症状同胞中识别中链酰基辅酶A脱氢酶缺乏症。
J Pediatr. 1986 Jan;108(1):13-8. doi: 10.1016/s0022-3476(86)80762-4.
5
Riboflavin-responsive ethylmalonic-adipic aciduria.核黄素反应性乙基丙二酸-己二酸尿症
J Inherit Metab Dis. 1985;8(2):67-70. doi: 10.1007/BF01801667.
6
Defects of metabolism of fatty acids in the sudden infant death syndrome.婴儿猝死综合征中脂肪酸代谢缺陷
Br Med J (Clin Res Ed). 1985 Jun 15;290(6484):1771-3. doi: 10.1136/bmj.290.6484.1771.
7
Dicarboxylic aciduria and medium chain triglyceride supplemented milk.二羧酸尿症与中链甘油三酯强化奶
Arch Dis Child. 1986 Jun;61(6):610-1. doi: 10.1136/adc.61.6.610.