TRANSIENT 5-OXOPROLINURIA IN A VERY-LOW-BIRTH-WEIGHT INFANT

被引：5

作者：

GOTO, A ^{[1
]}

ISHIDA, A ^{[1
]}

GOTO, R ^{[1
]}

HAYASAKA, K ^{[1
]}

NANAO, K ^{[1
]}

YAMASHITA, A ^{[1
]}

YAMAGUCHI, S ^{[1
]}

TAKADA, G ^{[1
]}

机构：

[1] GIFU UNIV,SCH MED,DEPT PEDIAT,GIFU 500,JAPAN

来源：

JOURNAL OF INHERITED METABOLIC DISEASE | 1992年 / 15卷 / 02期

关键词：

D O I：

10.1007/BF01799646

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：284 / 285

页数：2

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[1] 5-OXOPROLINURIA DUE TO HEREDITARY 5-OXOPROLINASE DEFICIENCY IN 2 BROTHERS - A NEW INBORN ERROR OF THE GAMMA-GLUTAMYL-TRANSFERASE CYCLE
LARSSON, A
MATTSSON, B
WAUTERS, EAK
VANGOOL, JD
DURAN, M
WADMAN, SK
[J]. ACTA PAEDIATRICA SCANDINAVICA, 1981, 70 (03): : 301 - 308
[2] GLUTATHIONE SYNTHETASE DEFICIENCY, AN INBORN ERROR OF METABOLISM INVOLVING GAMMA-GLUTAMYL CYCLE IN PATIENTS WITH 5-OXOPROLINURIA PYROGLUTAMIC ACIDURIA
WELLNER, VP
SEKURA, R
MEISTER, A
LARSSON, A
[J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1974, 71 (06) : 2505 - 2509