JUVENILE GM2 GANGLIOSIDOSIS - PARTIAL DEFICIENCY OF HEXOSAMINIDASE-A

被引:59
作者
OKADA, S
OBRIEN, JS
VEATH, ML
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D O I
10.1016/S0022-3476(70)80096-8
中图分类号
R72 [儿科学];
学科分类号
100202 ;
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页码:1063 / +
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共 7 条
[1]  
BERNHEIMER H, 1968, Wiener Klinische Wochenschrift, V80, P163
[2]   HURLERS SYNDROME - DEFICIENCY OF A SPECIFIC BETA GALACTOSIDASE ISOENZYME [J].
HO, MW ;
OBRIEN, JS .
SCIENCE, 1969, 165 (3893) :611-&
[3]  
MENKES JH, IN PRESS
[4]   TAY-SACHS DISEASE - DETECTION OF HETEROZYGOTES AND HOMOZYGOTES BY SERUM HEXOSAMINIDASE ASSAY [J].
OBRIEN, JS ;
OKADA, S ;
CHEN, A ;
FILLERUP, DL .
NEW ENGLAND JOURNAL OF MEDICINE, 1970, 283 (01) :15-&
[5]   TAY-SACHS DISEASE - GENERALIZED ABSENCE OF A BETA-D-N-ACEYLHEXOSAMINIDASE COMPONENT [J].
OKADA, S ;
OBRIEN, JS .
SCIENCE, 1969, 165 (3894) :698-&
[6]   JUVENILE GM2-GANGLIOSIDOSIS . CLINICAL VARIANT OF TAY-SACHS DISEASE OR A NEW DISEASE [J].
SUZUKI, K ;
SUZUKI, K ;
RAPIN, I ;
SUZUKI, Y ;
ISHII, N .
NEUROLOGY, 1970, 20 (02) :190-&
[7]  
VOLK BW, 1969, ARCH PATHOL, V87, P393