NEWBORN URINE SCREENING EXPERIENCE WITH OVER ONE MILLION INFANTS IN THE QUEBEC NETWORK OF GENETIC MEDICINE

被引：57

作者：

LEMIEUX, B ^{[1
]}

AURAYBLAIS, C ^{[1
]}

GIGUERE, R ^{[1
]}

SHAPCOTT, D ^{[1
]}

SCRIVER, CR ^{[1
]}

机构：

[1] MONTREAL CHILDRENS HOSP,DEBELLE LAB BIOCHEM GENET,MONTREAL H3H 1P3,QUEBEC,CANADA

来源：

JOURNAL OF INHERITED METABOLIC DISEASE | 1988年 / 11卷 / 01期

关键词：

D O I：

10.1007/BF01800056

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：45 / 55

页数：11

共 37 条

[11] A RAPID SCREENING TEST FOR DETECTION OF CONGENITAL METHYLMALONIC ACIDURIA IN INFANCY [J].

GIORGIO, AJ ;

LUHBY, L .

AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 1969, 52 (03) :374-&

[12] IMPROVED DIRECT METHOD FOR DETERMINATION OF KETO ACIDS BY 2,4-DINITROPHENYLHYDRAZINE [J].

KATSUKI, H ;

YOSHIDA, T ;

TANEGASHIMA, C ;

TANAKA, S .

ANALYTICAL BIOCHEMISTRY, 1971, 43 (02) :349-+

[13]

LABERGE C, 1975, UNION MED CAN, V104, P428

[14] ONTOGENY OF AMINO-ACID REABSORPTION IN HUMAN KIDNEY - EVIDENCE FROM THE HOMOZYGOUS INFANT WITH FAMILIAL RENAL IMINOGLYCINURIA FOR MULTIPLE PROLINE AND GLYCINE SYSTEMS [J].

LASLEY, L ;

SCRIVER, CR .

PEDIATRIC RESEARCH, 1979, 13 (01) :65-70

[15]

LEMIEUX B, 1984, J INHERIT METAB DIS, V7, P145

[16]

LEMIEUX B, 1983, UREA CYCLE DISEASE, P321

[17]

LEMIEUX B, 1974, VIE MED CANADA FRANC, V3, P321

[18]

Levy H.L., 1980, NEONATAL SCREENING I, P89

[19]

LEVY HL, 1984, PEDIATRICS, V74, P509

[20]

LEVY HL, 1972, PEDIATRICS, V49, P825

← 1 2 3 4 →