[Identification of aminoacidopathies using thin layer chromatography of urine].

A B Simonetti, A La Rocca Rossi
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Abstract

The aminoacidopathies, inborn errors of aminoacids metabolism, are rare pathological conditions that have mental retardation as secondarty cause. Using TLC with cellulose as adsorvent and using specific solvents and developer, we can obtain early diagnosis of a great number of those biochemical deviations. The authors based themselves in Ersser's publications to effect this research, now in its initial phase. The author's principal aim is to transform the semi-quantitative method into a quantitative one and to early diagnose the metabolic errors of aminoacids.

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[尿薄层色谱法鉴定氨基酸病]。
氨基酸缺乏症是一种罕见的以智力低下为继发原因的先天性氨基酸代谢异常的疾病。以纤维素为吸附剂,采用特定溶剂和显影剂的薄层色谱法,可以对大量的生化偏差进行早期诊断。作者根据厄瑟的出版物来影响这项研究,现在还处于初始阶段。作者的主要目的是将半定量方法转化为定量方法,早期诊断氨基酸代谢错误。
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