SUDDEN INFANT DEATH AND MULTIPLE ACYL-COA DEHYDROGENATION DISORDERS

被引：2

作者：

PARINI, R

VEGNI, C

MARTINI, J

ROMEO, A

GARAVAGLIA, B

机构：

[1] UNIV MILAN,SCH MED,IST CLIN PERFEZIONAMENTO,DEPT NEONATOL,I-20122 MILAN,ITALY

[2] UNIV MILAN,DEPT PATHOL,MILAN,ITALY

[3] OSPED REGINA ELENA,USSL 751,REG CTR CHILDHOOD EPILEPSY,MILAN,ITALY

[4] IST NEUROL CARLO BESTA,DEPT BIOCHEM & GENET,MILAN,ITALY

来源：

EUROPEAN JOURNAL OF PEDIATRICS | 1995年 / 154卷 / 05期

关键词：

D O I：

10.1007/BF02072123

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：421 / 422

页数：2

共 6 条

[1]

BOLES RG, 1994, IN PRESS HUM PATHOL, V25

[2] MUTATIONS AND POLYMORPHISMS OF THE GENE ENCODING THE BETA-SUBUNIT OF THE ELECTRON-TRANSFER FLAVOPROTEIN IN 3 PATIENTS WITH GLUTARIC ACIDEMIA TYPE-II [J].

COLOMBO, I ;

FINOCCHIARO, G ;

GARAVAGLIA, B ;

GARBUGLIO, N ;

YAMAGUCHI, S ;

FRERMAN, FE ;

BERRA, B ;

DIDONATO, S .

HUMAN MOLECULAR GENETICS, 1994, 3 (03) :429-435

[3]

DIDONATO S, 1988, NEUROLOGY, V38, P1107

[4] SUDDEN-INFANT-DEATH-SYNDROME AND MULTIPLE ACYL-COENZYME-A DEHYDROGENASE-DEFICIENCY, ETHYLMALONIC-ADIPIC ACIDURIA, OR SYSTEMIC CARNITINE DEFICIENCY [J].

HARPEY, JP ;

CHARPENTIER, C ;

COUDE, M ;

DIVRY, P ;

PATURNEAUJOUAS, M .

JOURNAL OF PEDIATRICS, 1987, 110 (06) :881-884

[5]

Pollitt R. J., 1993, Paediatrie und Paedologie, V28, P13

[6] RECOGNITION OF MEDIUM-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY IN ASYMPTOMATIC SIBLINGS OF CHILDREN DYING OF SUDDEN INFANT DEATH OR REYE-LIKE SYNDROMES [J].

ROE, CR ;

MILLINGTON, DS ;

MALTBY, DA ;

KINNEBREW, P .

JOURNAL OF PEDIATRICS, 1986, 108 (01) :13-18

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