3-METHYLGLUTACONIC ACIDURIA IN 2 INFANTS

被引：16

作者：

HAGBERG, B

HJALMARSON, O

LINDSTEDT, S

RANSNAS, L

STEEN, G

机构：

[1] GOTHENBURG UNIV,SAHLGRENS HOSP,DEPT CLIN CHEM,S-41345 GOTHENBURG,SWEDEN

[2] UNIV GOTHENBURG,EAST HOSP,DEPT PEDIAT 2,S-41685 GOTHENBURG,SWEDEN

来源：

CLINICA CHIMICA ACTA | 1983年 / 134卷 / 1-2期

关键词：

D O I：

10.1016/0009-8981(83)90184-5

中图分类号：

R446 [实验室诊断]; R-33 [实验医学、医学实验];

学科分类号：

1001 ;

摘要：

引用

收藏

页码：59 / 67

页数：9

相关论文

共 21 条

[1] DICROTALINE - THE STRUCTURE AND SYNTHESIS OF DICROTALIC ACID
ADAMS, R
VANDUUREN, BL
[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1953, 75 (10) : 2377 - 2379
[2] BJORKMAN L, 1976, CLIN CHEM, V22, P49
[3] COBURN HJ, 1973, CLIN CHEM, V19, P127
[4] ENZYME DEFECT IN SKIN FIBROBLASTS IN INTERMITTENT BRANCHED-CHAIN KETONURIA AND IN MAPLE SYRUP URINE DISEASE
DANCIS, J
HUTZLER, J
COX, RP
[J]. BIOCHEMICAL MEDICINE, 1969, 2 (05): : 407 - &
[5] 3-HYDROXY-3-METHYLGLUTARIC ACIDURIA COMBINED WITH 3-METHYLGLUTACONIC ACIDURIA - A NEW CASE
DIVRY, P
ROLLAND, MO
TEYSSIER, J
COTTE, J
FERNANDES, MCF
DEALMEIDA, IT
DASILVEIRA, C
[J]. JOURNAL OF INHERITED METABOLIC DISEASE, 1981, 4 (03) : 173 - 174
[6] 3-HYDROXY-3-METHYLGLUTARYL COENZYME-A LYASE DEFICIENCY - POSTNATAL MANAGEMENT FOLLOWING PRENATAL DIAGNOSIS BY ANALYSIS OF MATERNAL URINE
DURAN, M
SCHUTGENS, RBH
KETEL, A
HEYMANS, H
BERNTSSEN, MWJ
KETTING, D
WADMAN, SK
[J]. JOURNAL OF PEDIATRICS, 1979, 95 (06) : 1004 - 1007
[7] FAULL K, 1976, NEW ENGL J MED, V294, P1013
[8] GLUCOSE-METABOLISM IN A CHILD WITH "3-HYDROXY-3-METHYLGLUTARYL-COENZYME A LYASE DEFICIENCY
FRANCOIS, B
BACHMANN, C
SCHUTGENS, RBH
[J]. JOURNAL OF INHERITED METABOLIC DISEASE, 1981, 4 (03) : 163 - 164
[9] 3-METHYLGLUTACONIC ACIDURIA - REPORT ON A SIBSHIP WITH INFANTILE PROGRESSIVE ENCEPHALOPATHY
GRETER, J
HAGBERG, B
STEEN, G
SODERHJELM, U
[J]. EUROPEAN JOURNAL OF PEDIATRICS, 1978, 129 (04) : 231 - 238
[10] Grob K., 1980, J HIGH RESOLUT CHROM, V3, P493