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Systemic carnitine deficiency simulating Reye syndrome.

作者信息

Coates P M, Hale D E, Stanley C A, Glasgow A M

出版信息

J Pediatr. 1984 Oct;105(4):679. doi: 10.1016/s0022-3476(84)80460-6.

DOI:10.1016/s0022-3476(84)80460-6
PMID:6481556
Abstract
摘要

相似文献

1
Systemic carnitine deficiency simulating Reye syndrome.
J Pediatr. 1984 Oct;105(4):679. doi: 10.1016/s0022-3476(84)80460-6.
2
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.
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[Systemic carnitine deficiency: its place in Reye's syndrome (author's transl)].
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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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Amino acid pattern in Reye syndrome: comparison with clinically similar entities.
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6
Systemic carnitine deficiency as the cause of a prolonged illness and sudden death in a six-year-old child.系统性肉碱缺乏症作为一名六岁儿童长期患病及猝死的病因
J Inherit Metab Dis. 1985;8(3):159. doi: 10.1007/BF01819308.
7
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.
8
[Hyperammonemias of childhood. III. Acquired diseases].
Pediatr Pol. 1988 Mar;63(3):190-6.
9
Reye's syndrome or its metabolic mimics?
Hosp Pract (Off Ed). 1984 Sep;19(9):134F-134G, 134K, 134O.
10
Systemic carnitine deficiency: benefit of oral carnitine supplements vs. persisting biochemical abnormalities.
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引用本文的文献

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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
Skin fibroblast carnitine uptake in secondary carnitine deficiency disorders.继发性肉碱缺乏症中皮肤成纤维细胞的肉碱摄取
J Inherit Metab Dis. 1993;16(1):135-46. doi: 10.1007/BF00711327.
3
Catalytic defect of medium-chain acyl-coenzyme A dehydrogenase deficiency. Lack of both cofactor responsiveness and biochemical heterogeneity in eight patients.
中链酰基辅酶A脱氢酶缺乏症的催化缺陷。八例患者缺乏辅因子反应性和生化异质性。
J Clin Invest. 1985 Sep;76(3):963-9. doi: 10.1172/JCI112096.
4
Carnitine deficiency with cardiomyopathy presenting as neonatal hydrops: successful response to carnitine therapy.肉碱缺乏伴心肌病表现为新生儿水肿：对肉碱治疗的成功反应。
J Inherit Metab Dis. 1990;13(1):69-75. doi: 10.1007/BF01799334.
5
Interrelationships of liver and brain with special reference to Reye syndrome.
J Inherit Metab Dis. 1991;14(4):436-58. doi: 10.1007/BF01797917.