A modified automated fluorometric method for tyrosine determination in blood spotted on paper: a mass screening procedure for tyrosinemia.

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作者信息

Grenier A, Laberge C

出版信息

Clin Chim Acta. 1974 Nov 20;57(1):71-5. doi: 10.1016/0009-8981(74)90179-x.

DOI:10.1016/0009-8981(74)90179-x

PMID:4430143

Abstract

摘要

相似文献

A modified automated fluorometric method for tyrosine determination in blood spotted on paper: a mass screening procedure for tyrosinemia.

Clin Chim Acta. 1974 Nov 20;57(1):71-5. doi: 10.1016/0009-8981(74)90179-x.

alpha1-Fetoprotein measurement in blood spotted on paper: discriminating test for hereditary tyrosinemia in neonatal mass screening.

Clin Chem. 1976 Jul;22(7):1001-4.

[Hereditary tyrosinemia and alpha-1-fetoprotein. I. Clinical value of alpha-fetoprotein in hereditary tyrosinemia].

Pathol Biol (Paris). 1973 May;21(5):449-55.

Rapid automated quantitation of isoleucine, leucine, tyrosine and phenylalanine from dried blood filter paper specimens.从干血滤纸片标本中快速自动定量异亮氨酸、亮氨酸、酪氨酸和苯丙氨酸。

Clin Chim Acta. 1991 Dec 16;203(2-3):191-7. doi: 10.1016/0009-8981(91)90291-j.

Hereditary tyrosinemia. General discussion: screening aspects.遗传性酪氨酸血症。综述：筛查方面。

Can Med Assoc J. 1967 Oct 28;97(18):1096-8.

[Hereditary tyrosinemia. II. Presentation of a system of detection].

Pediatrie. 1973 Jan-Feb;28(1):19-22.

Fluorometric measurement of tyrosine in serum and plasma.血清和血浆中酪氨酸的荧光测定法。

Clin Chem. 1974 Apr;20(4):505-10.

Fumarylacetoacetase measurement as a mass-screening procedure for hereditary tyrosinemia type I.测定富马酰乙酰乙酸酶作为I型遗传性酪氨酸血症的大规模筛查方法。

Am J Hum Genet. 1990 Aug;47(2):325-8.

[Neonatal transitory tyrosinemia and other types of tyrosinemia].[新生儿暂时性酪氨酸血症及其他类型的酪氨酸血症]

Minerva Pediatr. 1976 Mar 31;28(11):637-43.

[Screening test for hyperphenylalaninemias and tyrosinemias : fluorometric micromethods for quantitative determination of phenylalanine and tyrosine by means of the same auto-analyzer system].[高苯丙氨酸血症和酪氨酸血症的筛查试验：利用同一自动分析仪系统定量测定苯丙氨酸和酪氨酸的荧光微量法]

Monatsschr Kinderheilkd (1902). 1977 May;125(5):475-7.

引用本文的文献

Screening for tyrosinaemia type I.I型酪氨酸血症筛查

Arch Dis Child Fetal Neonatal Ed. 1996 May;74(3):F191-4. doi: 10.1136/fn.74.3.f191.

Peripheral neuropathy as the presenting feature of tyrosinaemia type I and effectively treated with an inhibitor of 4-hydroxyphenylpyruvate dioxygenase.周围神经病变作为Ⅰ型酪氨酸血症的首发特征，并可通过4-羟基苯丙酮酸双加氧酶抑制剂得到有效治疗。

J Neurol Neurosurg Psychiatry. 1993 Oct;56(10):1129-32. doi: 10.1136/jnnp.56.10.1129.

Cord-blood tyrosine levels in the full-term phenylketonuric fetus and the "justification hypothesis".足月苯丙酮尿症胎儿的脐血酪氨酸水平与“合理性假说”

Proc Natl Acad Sci U S A. 1980 Oct;77(10):6175-8. doi: 10.1073/pnas.77.10.6175.

Fumarylacetoacetase measurement as a mass-screening procedure for hereditary tyrosinemia type I.测定富马酰乙酰乙酸酶作为I型遗传性酪氨酸血症的大规模筛查方法。

Am J Hum Genet. 1990 Aug;47(2):325-8.

Visceral pathology of hereditary tyrosinemia type I.I型遗传性酪氨酸血症的内脏病理学

Am J Hum Genet. 1990 Aug;47(2):317-24.

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