PARTIAL DEFICIENCY OF HEXOSAMINIDASE COMPONENT-A IN JUVENILE GM2-GANGLIOSIDOSIS

被引：73

作者：

SUZUKI, Y

SUZUKI, K

机构：

来源：

NEUROLOGY | 1970年 / 20卷 / 09期

关键词：

D O I：

10.1212/WNL.20.9.848

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

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页码：848 / &

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[1] ISOLATION OF BETA-N-ACETYLHEXOSAMINIDASE BETA-N-ACETYLGLUCOSAMINIDASE AND BETA-N-ACETYLGALACTOSAMINIDASE FROM CALF BRAIN
FROHWEIN, YZ
GATT, S
[J]. BIOCHEMISTRY, 1967, 6 (09) : 2775 - &
[2] ISOLATION OF BETA-GALACTOSIDASE AND BETA-GLUCOSIDASE FROM BRAIN
GATT, S
RAPPORT, MM
[J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1966, 113 (03) : 567 - &
[3] DEMONSTRATION OF AN ALTERATION OF GANGLIOSIDE METABOLISM IN TAY-SACHS DISEASE
KOLODNY, EH
BRADY, RO
VOLK, BW
[J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1969, 37 (03) : 526 - &
[4] OBRIEN JS, 1969, LANCET, V2, P805
[5] TAY-SACHS DISEASE - GENERALIZED ABSENCE OF A BETA-D-N-ACEYLHEXOSAMINIDASE COMPONENT
OKADA, S
OBRIEN, JS
[J]. SCIENCE, 1969, 165 (3894) : 698 - &
[6] TAY-SACHS DISEASE WITH A HEXOSAMINIDASE DEFECT
PILZ, H
MULLER, D
SANDHOFF, K
TERMEULE.V
[J]. DEUTSCHE MEDIZINISCHE WOCHENSCHRIFT, 1968, 93 (39) : 1833 - &
[7] DEFICIENT HEXOSAMINIDASE ACTIVITY IN AN EXCEPTIONAL CASE OF TAY-SACHS DISEASE WITH ADDITIONAL STORAGE OF KIDNEY GLOBOSIDE IN VISCERAL ORGANS
SANDHOFF, K
ANDREAE, U
JATZKEWITZ, H
[J]. LIFE SCIENCES PART 1 PHYSIOLOGY AND PHARMACOLOGY AND PART 2 BIOCHEMISTRY GENERAL AND MOLECULAR BIOLOGY, 1968, 7 (6P2): : 283 - +
[8] JUVENILE GM2-GANGLIOSIDOSIS . CLINICAL VARIANT OF TAY-SACHS DISEASE OR A NEW DISEASE
SUZUKI, K
SUZUKI, K
RAPIN, I
SUZUKI, Y
ISHII, N
[J]. NEUROLOGY, 1970, 20 (02) : 190 - &
[9] SUZUKI Y, TO BE PUBLISHED