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相似文献
1
Hyperammonaemia.高氨血症
Lancet. 1969 Jul 26;2(7613):196-7.
2
Biochemical investigations of hyperammonaemia.高氨血症的生化研究
Lancet. 1969 Jul 26;2(7613):170-4. doi: 10.1016/s0140-6736(69)91419-6.
3
Hyperammonemia: a deficiency of liver ornithine transcarbamylase.
Paediatr Univ Tokyo. 1970 Dec;18:167-73.
4
Inborn errors of urea synthesis.尿素合成的先天性缺陷。
Ann Neurol. 1994 Feb;35(2):133-41. doi: 10.1002/ana.410350204.
5
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.
6
[Hyperammonemia--congenital abnormality of the urea cycle].[高氨血症——尿素循环的先天性异常]
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7
Diagnosis of urea cycle disorders.尿素循环障碍的诊断。
Ann Clin Biochem. 1977 May;14(3):136-8. doi: 10.1177/000456327701400128.
8
Peritoneal dialysis in the reduction of blood ammonia levels in a case of hyperammonaemia.腹膜透析用于降低一例高氨血症患者的血氨水平。
Arch Dis Child. 1969 Apr;44(234):149-51. doi: 10.1136/adc.44.234.149.
9
Ornithine transcarbamylase deficiency: case report and review.鸟氨酸转氨甲酰酶缺乏症：病例报告与综述
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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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