苯甲酸钠和精氨酸：尿素合成先天性缺陷的替代途径疗法。 - Suppr

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超能文献

Sodium benzoate and arginine: alternative pathway therapy in inborn errors of urea synthesis.

作者信息

Batshaw M L

出版信息

Prog Clin Biol Res. 1983;127:69-83.

PMID:6889404

Abstract

摘要

相似文献

Sodium benzoate and arginine: alternative pathway therapy in inborn errors of urea synthesis.苯甲酸钠和精氨酸：尿素合成先天性缺陷的替代途径疗法。

Prog Clin Biol Res. 1983;127:69-83.

Treatment of inborn errors of urea synthesis: activation of alternative pathways of waste nitrogen synthesis and excretion.尿素合成先天性缺陷的治疗：激活废氮合成与排泄的替代途径。

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Treatment of episodic hyperammonemia in children with inborn errors of urea synthesis.尿素合成先天性代谢缺陷患儿发作性高氨血症的治疗

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Urea cycle enzymopathies.尿素循环酶病

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Amino acid acylation: a mechanism of nitrogen excretion in inborn errors of urea synthesis.氨基酸酰化：尿素合成先天性代谢异常中氮排泄的一种机制。

Science. 1980 Feb 8;207(4431):659-61. doi: 10.1126/science.6243418.

Arginine, an indispensable amino acid for patients with inborn errors of urea synthesis.精氨酸，对于尿素合成先天性代谢缺陷患者而言是一种必需氨基酸。

J Clin Invest. 1984 Dec;74(6):2144-8. doi: 10.1172/JCI111640.

[Urea cycle disorders].[尿素循环障碍]

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Management of heritable disorders of the urea cycle and of Refsum's and Fabry's diseases.

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Congenital hyperammonemic syndromes.先天性高氨血症综合征

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Simultaneous LC-MS/MS determination of phenylbutyrate, phenylacetate benzoate and their corresponding metabolites phenylacetylglutamine and hippurate in blood and urine.同时测定血和尿中的苯丁酸钠、苯乙酸盐、苯甲酸酯及其相应代谢物苯乙酰谷氨酰胺和马尿酸的 LC-MS/MS 法。

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J Inherit Metab Dis. 1998;21 Suppl 1:101-11. doi: 10.1023/a:1005365825875.

Excretion of hippuric acid during sodium benzoate therapy in patients with hyperglycinaemia or hyperammonaemia.高甘氨酸血症或高氨血症患者在苯甲酸钠治疗期间马尿酸的排泄情况。

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