LATE-ONSET GLOBOID-CELL LEUKODYSTROPHY - UNUSUAL ULTRASTRUCTURAL PATHOLOGY AND SUBTOTAL BETA-GALACTOCEREBROSIDASE DEFICIENCY

被引：16

作者：

GOEBEL, HH

HARZER, K

ERNST, JP

BOHL, J

KLEIN, H

机构：

[1] UNIV TUBINGEN,INST BRAIN RES,W-7400 TUBINGEN 1,GERMANY

[2] UNIV KIEL,DIV NEUROPEDIAT,W-2300 KIEL 1,GERMANY

[3] KRANKENHAUS BREMEN OST,INST CLIN NEUROPATHOL,BREMEN,GERMANY

来源：

JOURNAL OF CHILD NEUROLOGY | 1990年 / 5卷 / 04期

关键词：

D O I：

10.1177/088307389000500405

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：299 / 307

页数：9

共 19 条

[1] PERIPHERAL NEUROPATHY IN GLOBOID CELL LEUKODYSTROPHY (KRABBES DISEASE) . ULTRASTRUCTURAL AND HISTOCHEMICAL FINDINGS [J].

BISCHOFF, A ;

ULRICH, J .

BRAIN, 1969, 92 :861-&

[2] LATE ONSET GLOBOID-CELL LEUCODYSTROPHY [J].

CROME, L ;

HANEFELD, F ;

PATRICK, D ;

WILSON, J .

BRAIN, 1973, 96 (DEC) :841-&

[3] CONGENITAL MUSCLE FIBER-TYPE DISPROPORTION IN KRABBES LEUKODYSTROPHY [J].

DEHKHARGHANI, F ;

SARNAT, HB ;

BREWSTER, MA ;

ROTH, SI .

ARCHIVES OF NEUROLOGY, 1981, 38 (09) :585-587

[4] KRABBES LEUKODYSTROPHY WITHOUT GLOBOID-CELLS [J].

DUNN, HG ;

DOLMAN, CL ;

FARRELL, DF ;

TISCHLER, B ;

HASINOFF, C ;

WOOLF, LI .

NEUROLOGY, 1976, 26 (11) :1035-1041

[5] CLINICAL AND BIOCHEMICAL HETEROGENEITY OF GLOBOID-CELL LEUKODYSTROPHY [J].

FARRELL, DF ;

SWEDBERG, K .

ANNALS OF NEUROLOGY, 1981, 10 (04) :364-368

[6] LATE-ONSET KRABBE DISEASE INITIALLY DIAGNOSED AS CEREBROSIDE SULFATASE ACTIVATOR DEFICIENCY [J].

FLUHARTY, AL ;

NEIDENGARD, L ;

HOLTZMAN, D ;

KIHARA, H .

METABOLIC BRAIN DISEASE, 1986, 1 (03) :187-195

[7] KRABBES DISEASE - CLINICAL PRESENTATION OF NEUROLOGICAL VARIANTS [J].

HAGBERG, B .

NEUROPEDIATRICS, 1984, 15 :11-15

[8]

HANEFELD F, 1973, MONATSSCHR KINDERH, V121, P293

[9] PRENATAL ENZYMATIC DIAGNOSIS AND EXCLUSION OF KRABBES DISEASE (GLOBOID-CELL LEUKODYSTROPHY) USING CHORIONIC VILLI IN 5 RISK PREGNANCIES [J].

HARZER, K ;

HAGER, HD ;

TARIVERDIAN, G .

HUMAN GENETICS, 1987, 77 (04) :342-344

[10] SPHINGOLIPID ACTIVATOR PROTEIN-DEFICIENCY IN A 16-WEEK-OLD ATYPICAL GAUCHER DISEASE PATIENT AND HIS FETAL SIBLING - BIOCHEMICAL SIGNS OF COMBINED SPHINGOLIPIDOSES [J].

HARZER, K ;

PATON, BC ;

POULOS, A ;

KUSTERMANNKUHN, B ;

ROGGENDORF, W ;

GRISAR, T ;

POPP, M .

EUROPEAN JOURNAL OF PEDIATRICS, 1989, 149 (01) :31-39

← 1 2 →