EEG DEVELOPMENT IN RETT SYNDROME - A STUDY OF 30 CASES

被引：52

作者：

HAGNE, I

WITTENGERSTROM, I

HAGBERG, B

机构：

[1] GOTHENBURG UNIV,DEPT CLIN NEUROPHYSIOL,S-41124 GOTHENBURG,SWEDEN

[2] GOTHENBURG UNIV,DEPT PEDIAT 2,S-41124 GOTHENBURG,SWEDEN

来源：

ELECTROENCEPHALOGRAPHY AND CLINICAL NEUROPHYSIOLOGY | 1989年 / 72卷 / 01期

关键词：

D O I：

10.1016/0013-4694(89)90025-4

中图分类号：

R318 [生物医学工程];

学科分类号：

0831 ;

摘要：

引用

页码：1 / 6

页数：6

共 13 条

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GLAZE, DG ;

FROST, JD ;

ZOGHBI, HY ;

PERCY, AK .

ARCHIVES OF NEUROLOGY, 1987, 44 (10) :1053-1056

[2] A PROGRESSIVE SYNDROME OF AUTISM, DEMENTIA, ATAXIA, AND LOSS OF PURPOSEFUL HAND USE IN GIRLS - RETTS SYNDROME - REPORT OF 35 CASES [J].

HAGBERG, B ;

AICARDI, J ;

DIAS, K ;

RAMOS, O .

ANNALS OF NEUROLOGY, 1983, 14 (04) :471-479

[3] RETT SYNDROME - CRITERIA FOR INCLUSION AND EXCLUSION [J].

HAGBERG, B ;

GOUTIERES, F ;

HANEFELD, F ;

RETT, A ;

WILSON, J .

BRAIN & DEVELOPMENT, 1985, 7 (03) :372-373

[4] RETT SYNDROME - EPIDEMIOLOGY AND NOSOLOGY - PROGRESS IN KNOWLEDGE 1986 - A CONFERENCE COMMUNICATION [J].

HAGBERG, B ;

WITTENGERSTROM, I .

BRAIN & DEVELOPMENT, 1987, 9 (05) :451-457

[5]

HAGBERG B, 1986, AM J MED GENET S, V1

[6]

JELLINGER K, 1986, AM J MED GENET S1, V1

[7]

NIEDERMEYER E, 1986, AM J MED GENET S, V1

[8]

NOMURA Y, 1986, AM J MED GENET S1, V1

[9]

RETT A, 1966, EIN ZEREBRALATROPHIS

[10]

RIEDERER P, 1986, AM J MED GENET S1, V1

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