Paediatric screening for genetically determined metabolic diseases.
作者信息
Woolf L I
出版信息
Proc R Soc Med. 1968 Aug;61(8):766-7. doi: 10.1177/003591576806100811.
Abstract
摘要
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本文引用的文献
1
Phenylketonuria: a reassessment of mass infant screening by napkin test.苯丙酮尿症：通过尿片检测对大规模婴儿筛查的重新评估。
Br Med J. 1967 Sep 2;3(5565):582. doi: 10.1136/bmj.3.5565.582.
2
AN AUTOMATED PROCEDURE FOR BLOOD PHENYLALANINE.一种血液苯丙氨酸的自动化检测程序。
Clin Chem. 1965 May;11:541-6.
3
APPLICATION OF A SIMPLE MICROMETHOD TO THE SCREENING OF PLASMA FOR A VARIETY OF AMINOACIDOPATHIES.一种简单微量法在多种氨基酸病血浆筛查中的应用
Lancet. 1964 Aug 1;2(7353):230-2. doi: 10.1016/s0140-6736(64)90183-7.
4
A SIMPLE CHROMATOGRAPHIC SCREENING TEST FOR THE DETECTION OF DISORDERS OF AMINO ACID METABOLISM. A TECHNIC USING WHOLE BLOOD OR URINE COLLECTED ON FILTER PAPER.一种用于检测氨基酸代谢紊乱的简单色谱筛查试验。一种使用滤纸采集的全血或尿液的技术。
N Engl J Med. 1964 Jun 25;270:1378-83. doi: 10.1056/NEJM196406252702602.
5
Tests for phenylketonuria: results of a one-year programme for its detection in infancy and among mental defectives.苯丙酮尿症检测：一项针对婴儿期和智障人群进行为期一年的检测计划的结果
Br Med J. 1959 Sep 26;2(5151):532-5. doi: 10.1136/bmj.2.5151.532.
6
A manual fluorometric paper disc method for detecting phenylketonuria.
Clin Chem. 1967 Aug;13(8):621-5.
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