Coagulation defect of congenital tyrosinaemia.
作者信息
Ozsoylu S
出版信息
Arch Dis Child. 1985 Feb;60(2):188-9. doi: 10.1136/adc.60.2.188-b.
Abstract
摘要
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本文引用的文献
1
Coagulation defect of congenital tyrosinaemia.先天性酪氨酸血症的凝血缺陷
Arch Dis Child. 1984 Nov;59(11):1088-90. doi: 10.1136/adc.59.11.1088.
2
Evidence for liver disease preceding amino acid abnormalities in hereditary tyrosinemia.遗传性酪氨酸血症中肝脏疾病先于氨基酸异常出现的证据。
N Engl J Med. 1983 May 26;308(21):1265-7. doi: 10.1056/NEJM198305263082105.
3
Galactokinase deficiency: clinical and biochemical findings in a new kindred.半乳糖激酶缺乏症：一个新家族的临床和生化研究结果
J Pediatr. 1972 Jul;81(1):50-5. doi: 10.1016/s0022-3476(72)80373-1.
4
Acquired dysfibrinogenaemia in acute and chronic liver disease.急慢性肝病中的获得性异常纤维蛋白原血症
Br J Haematol. 1977 Feb;35(2):301-8. doi: 10.1111/j.1365-2141.1977.tb00586.x.
5
Tyrosine metabolism in cirrhosis.肝硬化中的酪氨酸代谢
J Lab Clin Med. 1979 Dec;94(6):832-40.
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