Demonstration of acid α-glucosidase in different types of Pompe disease by use of an immunochemical method
- 1 November 1984
- journal article
- research article
- Published by Elsevier in Journal of the Neurological Sciences
- Vol. 66 (2-3) , 129-139
- https://doi.org/10.1016/0022-510x(84)90001-7
Abstract
No abstract availableFunding Information
- Ministry of Education, Culture, Sports, Science and Technology (58480255)
This publication has 22 references indexed in Scilit:
- Immunohistochemical demonstration of acid α-glucosidase in muscle in Pompe's diseaseJournal of Molecular Histology, 1983
- Immunohistochemical localization of acid alpha-glucosidase in rat liver.Journal of Histochemistry & Cytochemistry, 1982
- Use of immobilized antibodies in investigating acid α-glucosidase in urine in relation to Pompe's diseaseBiochimica et Biophysica Acta (BBA) - Enzymology, 1979
- Characterization of the molecular defect in infantile and adult acid alpha-glucosidase deficiency fibroblasts.Journal of Clinical Investigation, 1978
- Lysosomal enzyme activities in cultured lymphoid cell linesClinica Chimica Acta; International Journal of Clinical Chemistry, 1977
- Some properties of human liver acid α-glucosidaseBiochimica et Biophysica Acta (BBA) - Enzymology, 1977
- Methods for analysis of acid alpha-1,4-glucosidase activity in single hybrid cells.Journal of Histochemistry & Cytochemistry, 1976
- The spectrum and diagnosis of acid maltase deficiencyNeurology, 1973
- Rodent and Human Acid α‐GlucosidaseEuropean Journal of Biochemistry, 1972
- A SIMPLE METHOD FOR PRODUCING ANTIBODY SPECIFIC TO A SINGLE SELECTED DIFFUSIBLE ANTIGENThe Lancet, 1966