An inherited enzyme deficiency resulting in hyperammonaemia and coma in a burn patient.
作者信息
Field T O, Dominic W J, Hansbrough J F
出版信息
Burns Incl Therm Inj. 1987 Jun;13(3):229-31. doi: 10.1016/0305-4179(87)90171-9.
PMID:3607566
Abstract
摘要
相似文献
1
An inherited enzyme deficiency resulting in hyperammonaemia and coma in a burn patient.
Burns Incl Therm Inj. 1987 Jun;13(3):229-31. doi: 10.1016/0305-4179(87)90171-9.
2
Continuous venovenous haemofiltration in hyperammonaemic coma of an adult with non-diagnosed partial ornithine transcarbamylase deficiency.成人未确诊的部分鸟氨酸转氨甲酰酶缺乏症高氨血症昏迷患者的持续静静脉血液滤过
Nephrol Dial Transplant. 1999 May;14(5):1282-4. doi: 10.1093/ndt/14.5.1282.
3
Partial ornithine transcarbamylase deficiency associated with recurrent hyperammonemia, lethargy and depressed sensorium.
Clin Genet. 1984 Jun;25(6):538-42. doi: 10.1111/j.1399-0004.1984.tb00498.x.
4
Ornithine transcarbamylase deficiency in a male: strict correlation between metabolic control and plasma arginine concentration.
Eur J Pediatr. 1989 Jan;148(4):349-52. doi: 10.1007/BF00444132.
5
Ornithine transcarbamylase deficiency in male adolescence and adulthood.男性青少年及成年期鸟氨酸转氨甲酰酶缺乏症
Enzyme. 1990;43(3):160-8. doi: 10.1159/000468724.
6
[Familial primary ornithine carbamoyltransferase defect].[家族性原发性鸟氨酸氨甲酰基转移酶缺陷]
Med Klin (Munich). 1986 Nov 11;81(23):767-70.
7
Failure of protein loading tests to identify heterozygosity for ornithine carbamoyltransferase deficiency.蛋白质负荷试验未能识别出鸟氨酸氨甲酰基转移酶缺乏症的杂合性。
J Inherit Metab Dis. 1984;7(4):157-9. doi: 10.1007/BF01805599.
8
[A new family with mutation of the structural gene of human ornithine carbamoyltransferase].[一个人类鸟氨酸氨甲酰基转移酶结构基因突变的新家族]
Arch Fr Pediatr. 1978 May;35(5):512-8.
9
Hyperammonemia due to a defect in hepatic ornithine transcarbamylase.由于肝脏鸟氨酸转氨甲酰酶缺陷导致的高氨血症。
Pediatrics. 1972 Jul;50(1):100-11.
10
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。
Eur J Pediatr. 1978 Jul 19;128(4):261-72. doi: 10.1007/BF00445611.
Zotero 插件