OCULAR FEATURES OF THE HAGBERG-SANTAVUORI SYNDROME

被引：10

作者：

BATEMAN, JB

PHILIPPART, M

机构：

[1] UNIV CALIF LOS ANGELES,DEPT OPHTHALMOL,LOS ANGELES,CA 90024

[2] UNIV CALIF LOS ANGELES,DEPT PSYCHIAT,LOS ANGELES,CA 90024

[3] UNIV CALIF LOS ANGELES,DEPT PEDIAT,LOS ANGELES,CA 90024

[4] UNIV CALIF LOS ANGELES,DEPT NEUROL,LOS ANGELES,CA 90024

来源：

AMERICAN JOURNAL OF OPHTHALMOLOGY | 1986年 / 102卷 / 02期

关键词：

D O I：

10.1016/0002-9394(86)90155-8

中图分类号：

R77 [眼科学];

学科分类号：

100212 ;

摘要：

引用

页码：262 / 271

页数：10

共 36 条

[11] LATE INFANTILE PROGRESSIVE ENCEPHALOPATHY WITH DISTURBED POLYUNSATURATED FAT METABOLISM [J].

HAGBERG, B ;

SOURANDER, P ;

SVENNERHOLM, L .

ACTA PAEDIATRICA SCANDINAVICA, 1968, 57 (06) :495-+

[12] 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

[13] INFANTILE TYPE OF SO-CALLED NEURONAL CEROID-LIPOFUSCINOSIS .2. MORPHOLOGICAL AND BIOCHEMICAL STUDIES [J].

HALTIA, M ;

RAPOLA, J ;

SANTAVUORI, P ;

KERANEN, A .

JOURNAL OF THE NEUROLOGICAL SCIENCES, 1973, 18 (03) :269-285

[14] LEBERS CONGENITAL AMAUROSIS AS A MANIFESTATION OF INFANTILE CEROID LIPOFUSCINOSIS (HALTIA-SANTAVUORI TYPE) [J].

HERRICK, MK ;

FORNO, LS ;

EGBERT, PR ;

URICH, H .

NEURO-OPHTHALMOLOGY, 1984, 4 (03) :151-163

[15] A late form of amaurotic idiocy and its heredofamiliar foundations [J].

Kufs, H .

ZEITSCHRIFT FUR DIE GESAMTE NEUROLOGIE UND PSYCHIATRIE, 1925, 95 :169-188

[16]

LIBERT J, 1977, ARCH OPHTALMOL-PARIS, V37, P613

[17] SO-CALLED NEURONAL CEROID LIPOFUSCINOSIS - NEUROPHYSIOLOGICAL STUDIES IN 60 CHILDREN [J].

PAMPIGLIONE, G ;

HARDEN, A .

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1977, 40 (04) :323-330

[18]

PAOLO J, 1982, NEUROLOGY, V32, P1035

[19]

PHILIPPART M, 1985, Journal of Neurology, V232, P44

[20]

RAITTA C, 1973, ACTA OPHTHALMOL, V51, P755

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