DIHYDROPYRIMIDINURIA - A NEW INBORN ERROR OF PYRIMIDINE METABOLISM

被引：33

作者：

DURAN, M ^{[1
]}

ROVERS, P ^{[1
]}

DEBREE, PK ^{[1
]}

SCHREUDER, CH ^{[1
]}

BEUKENHORST, H ^{[1
]}

DORLAND, L ^{[1
]}

BERGER, R ^{[1
]}

机构：

[1] HOSP ST JOANNES DEO,DEPT PAEDIAT,HAARLEM,NETHERLANDS

来源：

JOURNAL OF INHERITED METABOLIC DISEASE | 1991年 / 14卷 / 03期

关键词：

D O I：

10.1007/BF01811705

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

页码：367 / 370

页数：4

共 7 条

[1]

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[2] DIAGNOSIS OF INHERITED ADENYLOSUCCINASE DEFICIENCY BY THIN-LAYER CHROMATOGRAPHY OF URINARY IMIDAZOLES AND BY AUTOMATED CATION-EXCHANGE COLUMN CHROMATOGRAPHY OF PURINES [J].

DEBREE, PK ;

WADMAN, SK ;

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DEJONGE, HF .

CLINICA CHIMICA ACTA, 1986, 156 (03) :279-287

[3] FAMILIAL DEFICIENCY OF DIHYDROPYRIMIDINE DEHYDROGENASE - BIOCHEMICAL BASIS FOR FAMILIAL PYRIMIDINEMIA AND SEVERE 5-FLUOROURACIL-INDUCED TOXICITY [J].

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[4] PURIFICATION AND PROPERTIES OF 5,6-DIHYDROPYRIMIDINE AMIDOHYDROLASE FROM CALF LIVER [J].

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[5] DIHYDROPYRIMIDINE DEHYDROGENASE-ACTIVITY IN HUMAN-BLOOD MONONUCLEAR-CELLS [J].

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HRUSHESKY, WAM ;

SOTHERN, RB ;

ODEA, RF .

ENZYME, 1989, 42 (01) :15-24

[6] DIHYDROPYRIMIDINE DEHYDROGENASE-DEFICIENCY LEADING TO THYMINE-URACILURIA - AN INBORN ERROR OF PYRIMIDINE METABOLISM [J].

WADMAN, SK ;

BERGER, R ;

DURAN, M ;

DEBREE, PK ;

STOKERDEVRIES, SA ;

BEEMER, FA ;

WEITSBINNERTS, JJ ;

PENDERS, TJ ;

VANDERWOUDE, JK .

JOURNAL OF INHERITED METABOLIC DISEASE, 1985, 8 :113-114

[7]

WADMAN SK, 1989, HIGHLIGHTS MODERN BI, V2, P1379

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