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Systemic carnitine deficiency simulating recurrent Reye syndrome.

作者信息

Glasgow A M, Eng G, Engel A G

出版信息

J Pediatr. 1980 May;96(5):889-91. doi: 10.1016/s0022-3476(80)80571-3.

DOI:10.1016/s0022-3476(80)80571-3
PMID:7365598
Abstract
摘要

相似文献

1
Systemic carnitine deficiency simulating recurrent Reye syndrome.模拟复发性瑞氏综合征的全身性肉碱缺乏症。
J Pediatr. 1980 May;96(5):889-91. doi: 10.1016/s0022-3476(80)80571-3.
2
Systemic carnitine deficiency simulating Reye syndrome.
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[Systemic carnitine deficiency: its place in Reye's syndrome (author's transl)].
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4
Systemic carnitine deficiency.全身性肉碱缺乏症
Nutr Rev. 1981 Nov;39(11):400-2. doi: 10.1111/j.1753-4887.1981.tb06726.x.
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Systemic carnitine deficiency--a treatable inherited lipid-storage disease presenting as Reye's syndrome.系统性肉碱缺乏症——一种可治疗的遗传性脂质贮积病，表现为瑞氏综合征。
N Engl J Med. 1980 Dec 11;303(24):1389-94. doi: 10.1056/NEJM198012113032403.
6
Systemic carnitine deficiency: benefit of oral carnitine supplements vs. persisting biochemical abnormalities.
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Amino acid pattern in Reye syndrome: comparison with clinically similar entities.
J Pediatr. 1981 May;98(5):788-90. doi: 10.1016/s0022-3476(81)80849-9.
8
Reye's syndrome or its metabolic mimics?
Hosp Pract (Off Ed). 1984 Sep;19(9):134F-134G, 134K, 134O.
9
[Hyperammonemias of childhood. III. Acquired diseases].
Pediatr Pol. 1988 Mar;63(3):190-6.
10
Carnitine prevents Reye-like syndrome in atypical carnitine deficiency.
Pediatr Neurol. 1986 Mar-Apr;2(2):80-4. doi: 10.1016/0887-8994(86)90061-5.

引用本文的文献

1
Clinical characteristics of primary carnitine deficiency: A structured review using a case-by-case approach.原发性肉碱缺乏症的临床特征：基于案例的结构化综述。
J Inherit Metab Dis. 2022 May;45(3):386-405. doi: 10.1002/jimd.12475. Epub 2022 Feb 3.
2
Malignant cerebral edema secondary to hyperammonemia in setting of acquired carnitine deficiency.获得性肉碱缺乏情况下高氨血症继发的恶性脑水肿。
Neurol Clin Pract. 2020 Oct;10(5):e41-e43. doi: 10.1212/CPJ.0000000000000742.
3
Hyperammonemic encephalopathy caused by carnitine deficiency.
肉碱缺乏所致高氨血症性脑病
J Gen Intern Med. 2008 Feb;23(2):210-3. doi: 10.1007/s11606-007-0473-0. Epub 2007 Dec 13.
4
New developments in the diagnosis and investigation of mitochondrial fatty acid oxidation disorders.线粒体脂肪酸氧化障碍的诊断与研究新进展
Eur J Pediatr. 1994;153(7 Suppl 1):S49-56. doi: 10.1007/BF02138778.
5
Carnitine transport in cultured muscle cells and skin fibroblasts from patients with primary systemic carnitine deficiency.
In Vitro. 1982 May;18(5):495-500. doi: 10.1007/BF02796479.
6
Decreased serum carnitine in valproate induced Reye syndrome.丙戊酸盐诱发瑞氏综合征时血清肉碱降低。
Eur J Pediatr. 1982 Nov;139(3):185-6. doi: 10.1007/BF01377353.
7
Kinetic compartmental analysis of carnitine metabolism in the human carnitine deficiency syndromes. Evidence for alterations in tissue carnitine transport.人类肉碱缺乏综合征中肉碱代谢的动力学房室分析。组织肉碱转运改变的证据。
J Clin Invest. 1984 Mar;73(3):857-67. doi: 10.1172/JCI111281.
8
Systemic carnitine deficiency: benefit of oral carnitine supplements vs. persisting biochemical abnormalities.
Eur J Pediatr. 1984 Aug;142(3):224-8. doi: 10.1007/BF00442456.
9
Carnitine metabolism and inborn errors.
J Inherit Metab Dis. 1984;7 Suppl 1:38-43. doi: 10.1007/BF03047372.
10
Effect of Reye's syndrome serum on isolated chinchilla liver mitochondria.瑞氏综合征血清对离体龙猫肝线粒体的影响。
J Clin Invest. 1985 Aug;76(2):816-25. doi: 10.1172/JCI112039.