[Newborn infant screening program in Switzerland].

作者信息

Gitzelmann R

出版信息

Bull Schweiz Akad Med Wiss. 1972 Sep;28(5):294-301.

PMID:4645587

Abstract

摘要

相似文献

[Newborn infant screening program in Switzerland].

Bull Schweiz Akad Med Wiss. 1972 Sep;28(5):294-301.

[Screening and therapy of 6 metabolic diseases of hereditary nature which are possible causes of mental retardation: screening of 1,900,000 newborn infants since the year 1965].

Clin Ter. 1979 Mar 15;88(5):445-59.

[Methods and results of screening newborn infants for aminoacidopathies].

Monatsschr Kinderheilkd (1902). 1976 Sep;129(9):650-3.

[Laboratory examinations for inborn errors of metabolism].

Rinsho Byori. 1986 Feb;34(2):133-5.

[Diagnosis and therapy of 6 hereditary, to mental-deficiency-leading, metabolic disorders. 2].

Med Klin. 1976 Apr 30;71(18):779-85.

[Screening results for inborn errors of metabolism in Western Europe].

Monatsschr Kinderheilkd (1902). 1973 May;121(5):205-6.

[Screening studies in newborn infants].

Monatsschr Kinderheilkd. 1983 Nov;131(11):806-9.

Collective results of mass screening for inborn metabolic errors in eight European countries.

Acta Paediatr Scand. 1973 Jul;62(4):413-6. doi: 10.1111/j.1651-2227.1973.tb08129.x.

The Texas Newborn Screening Program.

Tex Med. 1983 Feb;79(2):44-6.

State screening for metabolic disorders in newborns.

Am Fam Physician. 1988 Apr;37(4):223-8.

引用本文的文献

Phenylketonuria variants in Ontario.

Can Med Assoc J. 1976 Sep 18;115(6):509-12.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验