Phenylketonuria. Mass screening of newborns in Ireland.
作者信息
Cahalane S F
出版信息
Arch Dis Child. 1968 Apr;43(228):141-4. doi: 10.1136/adc.43.228.141.
Abstract
摘要
相似文献
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Phenylketonuria. Mass screening of newborns in Ireland.苯丙酮尿症。爱尔兰新生儿群体筛查。
Arch Dis Child. 1968 Apr;43(228):141-4. doi: 10.1136/adc.43.228.141.
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本文引用的文献
1
Variations in intelligence in phenylktonuria.苯丙酮尿症患者智力的差异。
Can Med Assoc J. 1962 Apr 21;86(16):736-43.
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
NEWBORN PHENYLKETONURIA DETECTION PROGRAM IN MASSACHUSETTS.马萨诸塞州新生儿苯丙酮尿症检测项目
Am J Public Health Nations Health. 1964 Dec;54(12):2075-81. doi: 10.2105/ajph.54.12.2075.
4
CASE FINDING IN PHENYLKETONURIA. II. THE GUTHRIE TEST.苯丙酮尿症的病例发现。二、古思里试验。
Can Med Assoc J. 1964 Jul 18;91(3):105-14.
5
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.
6
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.
7
PHENYLKETONURIA: A REPORT ON THE GUTHRIE SCREENING TEST.苯丙酮尿症：关于古思里筛查试验的报告。
J Ir Med Assoc. 1964 Mar;54:88-9.
8
MATERNAL PHENYLKETONURIA. A CAUSE OF MENTAL RETARDATION IN CHILDREN WITHOUT THE METABOLIC DEFECT.母体苯丙酮尿症。一种导致无代谢缺陷儿童智力发育迟缓的原因。
N Engl J Med. 1963 Dec 26;269:1404-8. doi: 10.1056/NEJM196312262692604.
9
10
Atypical phenylketonuria in sisters with normal offspring.
Lancet. 1961 Aug 26;2(7200):464-5. doi: 10.1016/s0140-6736(61)92434-5.
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