Gangliosidosis with total hexosaminidase deficiency: Clinical, biochemical and ultrastructural studies and comparison with conventional cases of Tay-Sachs disease
- 1 January 1973
- journal article
- research article
- Published by Springer Nature in Acta Neuropathologica
- Vol. 23 (2), 118-132
- https://doi.org/10.1007/bf00685766
Abstract
No abstract availableKeywords
This publication has 39 references indexed in Scilit:
- ENZYME ALTERATIONS AND LIPID STORAGE IN THREE VARIANTS OF TAY‐SACHS DISEASEJournal of Neurochemistry, 1971
- The hydrolysis of Tay‐Sachs ganglioside (TSG) by human N‐acetyl‐β‐D‐hexosaminidase AFEBS Letters, 1970
- Diagnosis of Tay-SachsNature, 1969
- Demonstration of an alteration of ganglioside metabolism in Tay-Sachs diseaseBiochemical and Biophysical Research Communications, 1969
- FIVE GANGLIOSIDOSESThe Lancet, 1969
- Variation of β‐N‐acetylhexosaminidase‐pattern in Tay‐Sachs diseaseFEBS Letters, 1969
- Tay-Sachs Disease.Acta Paediatrica, 1966
- On a biochemically special form of infantile amaurotic idiocyBiochimica et Biophysica Acta, 1963
- THE USE OF LEAD CITRATE AT HIGH pH AS AN ELECTRON-OPAQUE STAIN IN ELECTRON MICROSCOPYThe Journal of cell biology, 1963
- The chemical structure of normal human brain and Tay-Sachs gangliosidesBiochemical and Biophysical Research Communications, 1962