How to detect maple-syrup urine disease in newborn infants.
作者信息
Fogelson M H
出版信息
Clin Pediatr (Phila). 1970 Sep;9(9):538. doi: 10.1177/000992287000900914.
PMID:5465716
Abstract
摘要
相似文献
1
How to detect maple-syrup urine disease in newborn infants.如何检测新生儿的枫糖尿症。
Clin Pediatr (Phila). 1970 Sep;9(9):538. doi: 10.1177/000992287000900914.
2
Maple syrup urine disease: rapid prenatal diagnosis by enzyme assay.
Humangenetik. 1973;19(1):127-8. doi: 10.1007/BF00295241.
3
Diagnostic significance of amniotic fluid amino acids.羊水氨基酸的诊断意义
Obstet Gynecol. 1971 Apr;37(4):550-4.
4
Rapid diagnosis of maple syrup urine disease (branched chain ketoaciduria) by micro-enzyme assay in leukocytes and fibroblasts.通过白细胞和成纤维细胞中的微酶分析法快速诊断枫糖尿症（支链酮酸尿症）
Clin Chim Acta. 1973 May 30;45(4):433-40. doi: 10.1016/0009-8981(73)90046-6.
5
Intermittent branched chain ketonuria (variant of maple syrup urine disease).间歇性支链酮尿症（枫糖尿症变异型）
Clin Biochem. 1971 Jun;4(2):52-8. doi: 10.1016/s0009-9120(71)90611-4.
6
Maple syrup urine disease: response to dietary modifications.枫糖尿症：对饮食调整的反应
J Am Osteopath Assoc. 1979 Sep;79(1):98-104.
7
[Screening of the Westphalia-Lippe newborns of 1977 for phenylketonuria, histidinemia, homocystinuria and maple syrup disease. Furthermore a pilot study of galactosemia and galactokinase deficiency disease].[对1977年威斯特法伦-利珀地区新生儿进行苯丙酮尿症、组氨酸血症、同型胱氨酸尿症和枫糖尿症筛查。此外，对半乳糖血症和半乳糖激酶缺乏症进行了一项试点研究]
MMW Munch Med Wochenschr. 1979 Jun 22;121(25):833-4.
8
Biochemical studies on a variant of branched chain ketoaciduria in a 19-year-old female.一名19岁女性分支链酮酸尿症变异型的生化研究。
Pediatrics. 1971 Nov;48(5):795-801.
9
Family with intermittent maple syrup urine disease.患有间歇性枫糖尿症的家族。
Arch Dis Child. 1973 Mar;48(3):225-8. doi: 10.1136/adc.48.3.225.
10
A new variety of maple syrup urine disease.枫糖尿症的一种新变种。
Ann Clin Biochem. 1977 May;14(3):146-8. doi: 10.1177/000456327701400133.
Zotero 插件