NEUROPATHOLOGICAL FINDINGS IN A CASE OF COMBINED DEFICIENCY OF SULFITE OXIDASE AND XANTHINE DEHYDROGENASE

被引：7

作者：

BARTH, PG

BEEMER, FA

CATS, BP

DURAN, M

WADMAN, SK

机构：

[1] UNIV UTRECHT,CHILDRENS HOSP HET WILHELMINA KINDERZIEKENHUIS,DEPT GEN PEDIAT,NIEUWE GRACHT 137,3512 LK UTRECHT,NETHERLANDS

[2] UNIV UTRECHT,CHILDRENS HOSP HET WILHELMINA KINDERZIEKENHUIS,DEPT NEONATOL,3512 LK UTRECHT,NETHERLANDS

[3] UNIV UTRECHT,CHILDRENS HOSP HET WILHELMINA KINDERZIEKENHUIS,DEPT INHERITED METAB DIS,3512 LK UTRECHT,NETHERLANDS

[4] UNIV AMSTERDAM,MED CTR,DIV PEDIAT NEUROL,AMSTERDAM,NETHERLANDS

[5] CLIN GENET CTR,3501 CA UTRECHT,NETHERLANDS

来源：

VIRCHOWS ARCHIV A-PATHOLOGICAL ANATOMY AND HISTOPATHOLOGY | 1985年 / 408卷 / 01期

关键词：

D O I：

10.1007/BF00739967

中图分类号：

R602 [外科病理学、解剖学]; R32 [人体形态学];

学科分类号：

100101 ;

摘要：

引用

页码：105 / 106

页数：2

共 5 条

[1] ABSENCE OF HEPATIC MOLYBDENUM COFACTOR - AN INBORN ERROR OF METABOLISM ASSOCIATED WITH LENS DISLOCATION [J].

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OPHTHALMIC PAEDIATRICS AND GENETICS, 1985, 5 (03) :191-195

[2] INBORN-ERRORS OF MOLYBDENUM METABOLISM - COMBINED DEFICIENCIES OF SULFITE OXIDASE AND XANTHINE DEHYDROGENASE IN A PATIENT LACKING THE MOLYBDENUM COFACTOR [J].

JOHNSON, JL ;

WAUD, WR ;

RAJAGOPALAN, KV ;

DURAN, M ;

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WADMAN, SK .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (06) :3715-3719

[3] NEUROPATHOLOGIC CHANGES IN A CASE OF SULFITE OXIDASE DEFICIENCY [J].

ROSENBLUM, WI .

NEUROLOGY, 1968, 18 (12) :1187-+

[4] ANATOMO-PATHOLOGICAL FINDINGS IN A CASE OF COMBINED DEFICIENCY OF SULFITE OXIDASE AND XANTHINE-OXIDASE WITH A DEFECT OF MOLYBDENUM COFACTOR [J].

ROTH, A ;

NOGUES, C ;

MONNET, JP ;

OGIER, H ;

SAUDUBRAY, JM .

VIRCHOWS ARCHIV A-PATHOLOGICAL ANATOMY AND HISTOPATHOLOGY, 1985, 405 (03) :379-386

[5] ABSENCE OF HEPATIC MOLYBDENUM COFACTOR - AN INBORN ERROR OF METABOLISM LEADING TO A COMBINED DEFICIENCY OF SULFITE OXIDASE AND XANTHINE DEHYDROGENASE [J].

WADMAN, SK ;

DURAN, M ;

BEEMER, FA ;

CATS, BP ;

JOHNSON, JL ;

RAJAGOPALAN, KV ;

SAUDUBRAY, JM ;

OGIER, H ;

CHARPENTIER, C ;

BERGER, R ;

SMIT, GPA ;

WILSON, J ;

KRYWAWYCH, S .

JOURNAL OF INHERITED METABOLIC DISEASE, 1983, 6 :78-83

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