Periodic attacks of lethargy in a baby with ammonia intoxication due to a congenital defect in ureogenesis.
作者信息
Corbeel L M, Colombo J P, Van Sande M, Weber A
出版信息
Arch Dis Child. 1969 Dec;44(238):681-7. doi: 10.1136/adc.44.238.681.
Abstract
摘要
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Periodic attacks of lethargy in a baby with ammonia intoxication due to a congenital defect in ureogenesis.一名因先天性尿素生成缺陷导致氨中毒的婴儿出现周期性嗜睡发作。
Arch Dis Child. 1969 Dec;44(238):681-7. doi: 10.1136/adc.44.238.681.
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Attempted dietary treatment of a boy with hyperammonemia due to ornithine transferase deficiency.尝试对一名因鸟氨酸转移酶缺乏导致高氨血症的男孩进行饮食治疗。
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本文引用的文献
1
Argininosuccinate synthetase activity and citrulline metabolism in cells cultured from a citrullinemic subject.来自一名瓜氨酸血症患者的培养细胞中的精氨琥珀酸合成酶活性和瓜氨酸代谢
Proc Natl Acad Sci U S A. 1967 Mar;57(3):829-34. doi: 10.1073/pnas.57.3.829.
2
Adaptive characteristics of urea cycle enzymes in the rat.大鼠尿素循环酶的适应性特征
J Biol Chem. 1962 Feb;237:459-68.
3
ARGININOSUCCINIC ACIDURIA. ARGININOSUCCINASE AND ARGINASE IN HUMAN BLOOD CELLS.精氨基琥珀酸尿症。人血细胞中的精氨基琥珀酸酶和精氨酸酶。
Clin Sci. 1964 Apr;26:261-9.
4
[A micromethod for determining ornithine carbamoyltransferase (OCT) in blood and cerebrospinal fluid].
Klin Wochenschr. 1963 Jan 1;41:37-40. doi: 10.1007/BF01478619.
5
Hyperammonaemia. A new instance of an inborn enzymatic defect of the biosynthesis of urea.高氨血症。尿素生物合成先天性酶缺陷的一个新病例。
Lancet. 1962 Oct 6;2(7258):699-700. doi: 10.1016/s0140-6736(62)90508-1.
6
Comparative biochemistry of urea synthesis. I. Methods for the quantitative assay of urea cycle enzymes in liver.尿素合成的比较生物化学。I. 肝脏中尿素循环酶的定量测定方法。
J Biol Chem. 1959 Jul;234(7):1769-74.
7
Kinetics of ammonia metabolism in vivo.体内氨代谢的动力学
J Biol Chem. 1958 May;232(1):303-14.
8
The measurement of ammonia in whole blood, erythrocytes, and plasma.全血、红细胞和血浆中氨的测定。
J Lab Clin Med. 1957 Jun;49(6):962-74.
9
Hyperammonaemia. A variant type of deficiency of liver ornithine transcarbamylase.高氨血症。肝脏鸟氨酸转氨甲酰酶缺乏的一种变异类型。
Arch Dis Child. 1969 Apr;44(234):162-9. doi: 10.1136/adc.44.234.162.
10
Hyperammonaemia: a deficiency of liver ornithine transcarbamylase. Occurrence in mother and child.高氨血症：肝脏鸟氨酸转氨甲酰酶缺乏。母婴发病情况。
Arch Dis Child. 1969 Apr;44(234):152-61. doi: 10.1136/adc.44.234.152.
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