Gangliosidosis with total hexosaminidase deficiency: clinical, biochemical and ultrastructural studies and comparison with conventional cases of Tay-Sachs disease

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Published in:Acta neuropathologica 1973-01, Vol.23 (2), p.118-132
Main Authors: Fontaine, G, Résibois, A, Tondeur, M, Jonniaux, G, Farriaux, J P, Voet, W, Maillard, E, Loeb, H
Format: Article
Language:English
Subjects:
Biopsy
Brain Chemistry
Child
Chromatography, Thin Layer
Endothelium - enzymology
Frontal Lobe - enzymology
Gangliosides - metabolism
Hexosaminidases - metabolism
Histocytochemistry
Humans
Inclusion Bodies - analysis
Kupffer Cells - enzymology
Lipidoses - enzymology
Lipidoses - pathology
Lipids - analysis
Liver - enzymology
Lysosomes - enzymology
Microscopy, Electron
Neuroglia - enzymology
Neurons - enzymology
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cites cdi_FETCH-LOGICAL-c282t-52cec2f39806e6007b25d12552cd1980543e4ee3cc3516e5b56b0c2624c6c3ed3
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container_issue 2
container_start_page 118
container_title Acta neuropathologica
container_volume 23
creator Fontaine, G
Résibois, A
Tondeur, M
Jonniaux, G
Farriaux, J P
Voet, W
Maillard, E
Loeb, H
description
doi_str_mv 10.1007/BF00685766
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source Springer LINK Archives
subjects Biopsy
Brain Chemistry
Child
Chromatography, Thin Layer
Endothelium - enzymology
Frontal Lobe - enzymology
Gangliosides - metabolism
Hexosaminidases - metabolism
Histocytochemistry
Humans
Inclusion Bodies - analysis
Kupffer Cells - enzymology
Lipidoses - enzymology
Lipidoses - pathology
Lipids - analysis
Liver - enzymology
Lysosomes - enzymology
Microscopy, Electron
Neuroglia - enzymology
Neurons - enzymology
title Gangliosidosis with total hexosaminidase deficiency: clinical, biochemical and ultrastructural studies and comparison with conventional cases of Tay-Sachs disease
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