Prenatal exclusion of primary hyperoxaluria type 1.
作者信息
Danpure C J, Jennings P R, Penketh R J, Wise P J, Rodeck C H
出版信息
Lancet. 1988 Feb 13;1(8581):367. doi: 10.1016/s0140-6736(88)91171-3.
PMID:2893183
Abstract
摘要
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Prenatal exclusion of primary hyperoxaluria type 1.产前排除1型原发性高草酸尿症
Lancet. 1988 Feb 13;1(8581):367. doi: 10.1016/s0140-6736(88)91171-3.
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What are the present possibilities for the prenatal diagnosis of primary hyperoxaluria?目前产前诊断原发性高草酸尿症的可能性有哪些？
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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。
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Strategies for the prenatal diagnosis of primary hyperoxaluria type 1.1型原发性高草酸尿症的产前诊断策略。
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[Oxalosis (type 1 primary hyperoxaluria)].[草酸尿症（1型原发性高草酸尿症）]
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Enzymatic prenatal diagnosis of primary hyperoxaluria type 1: potential and limitations.1型原发性高草酸尿症的酶促产前诊断：潜力与局限性
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Polymorphisms in the alanine:glyoxylate aminotransferase gene and their application to the prenatal diagnosis of primary hyperoxaluria type 1.丙氨酸：乙醛酸转氨酶基因多态性及其在1型原发性高草酸尿症产前诊断中的应用。
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Molecular characterization and clinical use of a polymorphic tandem repeat in an intron of the human alanine:glyoxylate aminotransferase gene.人丙氨酸：乙醛酸转氨酶基因内含子中一个多态性串联重复序列的分子特征及临床应用
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[Type I oxalosis in childhood--studies within the scope of terminal renal failure in the child].[儿童I型草酸盐中毒——儿童终末期肾衰竭范围内的研究]
Klin Wochenschr. 1989 Nov 17;67(22):1156-67. doi: 10.1007/BF01726118.
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Enzymatic prenatal diagnosis of primary hyperoxaluria type 1: potential and limitations.1型原发性高草酸尿症的酶促产前诊断：潜力与局限性
J Inherit Metab Dis. 1989;12 Suppl 2:286-8. doi: 10.1007/BF03335400.
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Recent advances in the understanding, diagnosis and treatment of primary hyperoxaluria type 1.1型原发性高草酸尿症在理解、诊断和治疗方面的最新进展。
J Inherit Metab Dis. 1989;12(2):210-24. doi: 10.1007/BF01800727.
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