Animal model of human disease Gm2-gangliosidoses (amaurotic idiocies) types I, II, and 3.
作者信息
Karbe E
出版信息
Am J Pathol. 1973 Apr;71(1):151-4.
Abstract
摘要
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Animal model of human disease Gm2-gangliosidoses (amaurotic idiocies) types I, II, and 3.
Am J Pathol. 1973 Apr;71(1):151-4.
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本文引用的文献
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[Familial glycosphingolipoidosis of the dog (Juvenile amaurotic idiocy)].
Ergeb Allg Pathol Pathol Anat. 1966;47:1-43.
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[On the behavior of brain gangliosides in 2 cases of late infantile amaurotic idiocy].
Wien Klin Wochenschr. 1968 Mar 1;80(9):163-4 passim.
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Deficient hexozaminidase activity in an exceptional case of Tay-Sachs disease with additional storage of kidney globoside in visceral organs.
Life Sci. 1968 Mar 15;7(6):283-8. doi: 10.1016/0024-3205(68)90024-6.
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Familial amaurotic idiocy in male German shorthair pointers.
Pathol Vet. 1967;4(3):223-32. doi: 10.1177/030098586700400302.
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Ganglioside-storage diseases.
N Engl J Med. 1971 Apr 22;284(15):893-6. doi: 10.1056/NEJM197104222841607.
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[Morphological and neurochemical investigations of 2 types of amaurotic idiocy in the dog. Evidence of a GM2-gangliosidosis].
Acta Neuropathol. 1970;16(3):243-61. doi: 10.1007/BF00687364.
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Juvenile GM2 gangliosidosis. Biochemical and ultrastructural studies on a new variant of Tay-Sachs disease.
Arch Neurol. 1971 Jul;25(1):14-22. doi: 10.1001/archneur.1971.00490010024003.
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Ganglioside storage diseases.
Fed Proc. 1971 May-Jun;30(3):956-69.
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Gm2-gangliosidosis with total hexosaminidase deficiency.
Neurology. 1971 Apr;21(4):313-28. doi: 10.1212/wnl.21.4.313.
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