SCREENING FOR TETRAHYDROBIOPTERIN DEFICIENCY IN NEWBORNS USING DRIED URINE ON FILTER-PAPER

被引:23
作者
BLAU, N
KIERAT, L
HEIZMANN, CW
ENDRES, W
GIUDICI, T
WANG, M
机构
[1] UNIV MUNICH,DEPT PEDIAT,W-8000 MUNICH 2,GERMANY
[2] CHILDRENS HOSP,DIV MED GENET,LOS ANGELES,CA 90027
[3] WUHAN MED COLL,DEPT PEDIAT,HUBEI,PEOPLES R CHINA
关键词
D O I
10.1007/BF02435988
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
[No abstract available]
引用
收藏
页码:402 / 404
页数:3
相关论文
共 8 条
[1]  
BLAU N, 1988, ANNU REV NUTR, V8, P185
[2]   PRIMAPTERINURIA - A NEW VARIANT OF ATYPICAL PHENYLKETONURIA [J].
BLAU, N ;
CURTIUS, HC ;
KUSTER, T ;
MATASOVIC, A ;
SCHOEDON, G ;
DHONDT, JL ;
GUIBAUD, P ;
GIUDICI, T ;
BLASKOVICS, M .
JOURNAL OF INHERITED METABOLIC DISEASE, 1989, 12 :335-338
[3]   STRATEGY FOR THE SCREENING OF TETRAHYDROBIOPTERIN DEFICIENCY AMONG HYPERPHENYLALANINAEMIC PATIENTS - 15-YEARS EXPERIENCE [J].
DHONDT, JL .
JOURNAL OF INHERITED METABOLIC DISEASE, 1991, 14 (02) :117-127
[4]   BLOOD SPOTS ON GUTHRIE CARDS CAN BE USED FOR INHERITED TETRAHYDROBIOPTERIN DEFICIENCY SCREENING IN HYPERPHENYLALANINEMIC INFANTS [J].
LEEMING, RJ ;
BARFORD, PA ;
BLAIR, JA ;
SMITH, I .
ARCHIVES OF DISEASE IN CHILDHOOD, 1984, 59 (01) :58-61
[5]   DIAGNOSIS OF VARIANT FORMS OF HYPERPHENYLALANINEMIA USING FILTER-PAPER SPOTS OF URINE [J].
NARISAWA, K ;
HAYAKAWA, H ;
ARAI, N ;
MATSUO, N ;
TANAKA, T ;
NARITOMI, K ;
TADA, K .
JOURNAL OF PEDIATRICS, 1983, 103 (04) :577-579
[6]  
Naylor EW, 1989, CURRENT TRENDS INFAN, P89
[7]   HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY WITH COLUMN SWITCHING FOR THE ANALYSIS OF BIOGENIC-AMINE METABOLITES AND PTERINS [J].
NIEDERWIESER, A ;
STAUDENMANN, W ;
WETZEL, E .
JOURNAL OF CHROMATOGRAPHY, 1984, 290 (MAY) :237-246
[8]  
SCRIVER CR, 1989, METABOLIC BASIS INHE, P495