Rapid identification of primary hyperoxaluria type I patients using a novel, fully automated method for measurement of hepatic alanine: glyoxylate aminotransferase.
作者信息
Horváth V A, Wanders R J
机构信息
Department of Pediatrics and Clinical Biochemistry, University Hospital Amsterdam, The Netherlands.
出版信息
J Inherit Metab Dis. 1994;17(3):336-8. doi: 10.1007/BF00711823.
PMID:7807946
Abstract
摘要
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本文引用的文献
1
Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I.原发性高草酸尿症I型中的过氧化物酶体丙氨酸：乙醛酸转氨酶缺乏症
FEBS Lett. 1986 May 26;201(1):20-4. doi: 10.1016/0014-5793(86)80563-4.
2
Alanine glyoxylate aminotransferase and the urinary excretion of oxalate and glycollate in hyperoxaluria type I and the Zellweger syndrome.I型高草酸尿症和泽尔韦格综合征中的丙氨酸乙醛酸转氨酶以及草酸盐和乙醇酸盐的尿排泄
Clin Chim Acta. 1987 Jun 15;165(2-3):311-9. doi: 10.1016/0009-8981(87)90176-8.
3
A new micro-assay for human liver alanine: glyoxylate aminotransferase.一种检测人肝脏丙氨酸：乙醛酸转氨酶的新型微量测定法。
Clin Chim Acta. 1987 Dec;170(2-3):187-93. doi: 10.1016/0009-8981(87)90127-6.
4
Further studies on the activity and subcellular distribution of alanine:glyoxylate aminotransferase in the livers of patients with primary hyperoxaluria type 1.1型原发性高草酸尿症患者肝脏中丙氨酸：乙醛酸氨基转移酶活性及亚细胞分布的进一步研究
Clin Sci (Lond). 1988 Sep;75(3):315-22. doi: 10.1042/cs0750315.
5
Human liver L-alanine-glyoxylate aminotransferase: characteristics and activity in controls and hyperoxaluria type I patients using a simple spectrophotometric method.人肝脏L-丙氨酸-乙醛酸氨基转移酶：采用简单分光光度法对对照者和I型高草酸尿症患者的特征及活性研究
Clin Chim Acta. 1990 Aug 15;189(2):139-44. doi: 10.1016/0009-8981(90)90084-6.
6
Micromethod for the assay of glutamate: glyoxylate aminotransferase and modifications of a micromethod for the assay of alanine: glyoxylate aminotransferase. Implications for the prenatal diagnosis of type I hyperoxaluria by fetal liver biopsy.谷氨酸测定的微量方法：乙醛酸转氨酶以及丙氨酸：乙醛酸转氨酶测定微量方法的改进。对通过胎儿肝活检进行I型高草酸尿症产前诊断的意义。
Clin Chim Acta. 1991 Nov 9;203(1):105-6. doi: 10.1016/0009-8981(91)90164-8.
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