INFANTILE FORM OF SC NEURONAL CEROID-LIPOFUSCINOSIS

被引：0

作者：

ELLEDER, M

BRACHFELD, K

JIRASEK, A

SMID, F

机构：

[1] UNIV KARLOVY, FAK VSEOBECNEHO LEKARSTVI, HLAVUV PATOL ANAT USTAV, CS--12800 PRAHA 2, CZECHOSLOVAKIA

[2] UNIV KARLOVY, FAK DETSKEHO LEKARSTVI, NEUROL KLIN, CS-12800 PRAHA 2, CZECHOSLOVAKIA

来源：

SBORNIK LEKARSKY | 1976年 / 78卷 / 11-1期

关键词：

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：316 / +

页数：1

共 8 条

[1] CYTOSOME MORPHOLOGY AND DISTRIBUTION OF GENERALIZED CEROIDLIPOFUSCINOSIS IN A 28 MONTH OLD BOY WITH NORMAL MYELOPEROXIDASE ACTIVITY [J].

ANZIL, AP ;

BLINZINGER, K ;

HARZER, K ;

REITHER, M ;

ZIMMERMANN, G .

NEUROPADIATRIE, 1975, 6 (03) :259-283

[2] TYPE OF JUVENILE CEREBROMACULAR DEGENERATION CHARACTERIZED BY GRANULAR OSMIOPHILIC DEPOSITS [J].

CARPENTER, S ;

KARPATI, G ;

WOLFE, LS ;

ANDERMANN, F .

JOURNAL OF THE NEUROLOGICAL SCIENCES, 1973, 18 (01) :67-87

[3]

ELLEDER M, UNPUBLISHED

[4]

ELLEDER M, IN PRESS

[5] INFANTILE TYPE OF SO-CALLED NEURONAL CEROID-LIPOFUSCINOSIS - HISTOLOGICAL AND ELECTRON-MICROSCOPIC STUDIES [J].

HALTIA, M ;

RAPOLA, J ;

SANTAVUORI, P .

ACTA NEUROPATHOLOGICA, 1973, 26 (02) :157-170

[6] INFANTILE TYPE OF SO-CALLED NEURONAL CEROID-LIPOFUSCINOSIS .1. CLINICAL STUDY OF 15 PATIENTS [J].

SANTAVUORI, P ;

HALTIA, M ;

RAPOLA, J ;

RAITTA, C .

JOURNAL OF THE NEUROLOGICAL SCIENCES, 1973, 18 (03) :257-267

[7]

SEITELBERGER F, 1967, INBORN DISORDERS SPH, P43

[8]

ZEMAN W, 1969, PEDIATRICS, V44, P570

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