Lipids and Lipidoses 1967
DOI: 10.1007/978-3-642-87367-6_8
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Gangliosidoses

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Cited by 6 publications
(2 citation statements)
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“…Tay-Sachs' disease, an example of ganglioside storage, is considered by many investigators to result from a deficiency in one or several specific hydrolytic enzymes (39). All workers agree that metabolic intermediates accumulate in association with the appearance of membranous cytoplasmic bodies (myelin figures) in the central nervous system.…”
Section: Discussionmentioning
confidence: 99%
“…Tay-Sachs' disease, an example of ganglioside storage, is considered by many investigators to result from a deficiency in one or several specific hydrolytic enzymes (39). All workers agree that metabolic intermediates accumulate in association with the appearance of membranous cytoplasmic bodies (myelin figures) in the central nervous system.…”
Section: Discussionmentioning
confidence: 99%
“…This may be due in part to the various methods of fixation (see above) and in part to examination of various types of mucopolysaccharidosis, particularly in the early-examined cases where a differentiation of the various types was not possible, most cases being described as gargoylism but probably being mainly cases of Hurler's syndrome. The histochemical methods applied, yielding varying results, have given evidence of the disease being a lipidosis, a glycogenosis, a mucoproteinosis and a mucopolysaccharidosis (9, 10, 12, 38, 41, 60,61,64,68,75). The PAS-reaction has always been applied in these investigations.…”
Section: B the Stored Materials In Mucopolysaccha-mentioning
confidence: 99%