CYTOCHROME-C OXIDASE DEFICIENCY IN 3 PATIENTS WITH LEIGHS DISEASE

被引：8

作者：

DIROCCO, M

VENESELLI, E

CICCONE, MO

TACCONE, A

STROPPIANO, M

COTTAFAVA, F

机构：

[1] IST GIANNINA GASLINI,DIV NEUROPSICHIAT INFANTILE,I-16148 GENOA,ITALY

[2] IST GIANNINA GASLINI,SERV RADIOL,I-16148 GENOA,ITALY

[3] IST GIANNINA GASLINI,PEDIAT CLIN 1,I-16148 GENOA,ITALY

来源：

JOURNAL OF INHERITED METABOLIC DISEASE | 1988年 / 11卷

关键词：

D O I：

10.1007/BF01804232

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：189 / 192

页数：4

共 8 条

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HAYMOND, MW ;

OBERT, KA ;

NELSON, JS ;

PAGLIARA, AS .

ANNALS OF NEUROLOGY, 1979, 6 (06) :483-494

[2]

DIMAURO S, 1987, ANN NEUROL, V22, P438

[3]

FARMER TW, 1973, NEUROLOGY, V23, P429

[4] STUDIES ON PYRUVATE-CARBOXYLASE, PYRUVATE DECARBOXYLASE AND LIPOAMIDE DEHYDROGENASE IN SUB-ACUTE NECROTIZING ENCEPHALOMYELOPATHY [J].

HANSEN, TL ;

CHRISTENSEN, E ;

BRANDT, NJ .

ACTA PAEDIATRICA SCANDINAVICA, 1982, 71 (02) :263-267

[5] LEIGHS ENCEPHALOMYELOPATHY - AN INBORN ERROR OF GLUCONEOGENESIS [J].

HOMMES, FA ;

POLMAN, HA ;

REERINK, JD .

ARCHIVES OF DISEASE IN CHILDHOOD, 1968, 43 (230) :423-&

[6]

PINCUS JH, 1974, NEUROLOGY, V24, P855

[7]

Warton D.C., 1967, METHOD ENZYMOL, V10, P245

[8]

WILLEMS JL, 1977, PEDIATRICS, V60, P850

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