A mucopolysaccharide storage disease with involvement of the renal glomerular epithelium
- 30 April 1973
- journal article
- research article
- Published by Elsevier in The American Journal of Medicine
- Vol. 54 (4) , 549-556
- https://doi.org/10.1016/0002-9343(73)90053-3
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Inborn Errors of Mucopolysaccharide MetabolismScience, 1970
- The nosology of the mucopolysaccharidosesThe American Journal of Medicine, 1969
- The Abnormalities of Lysosomal Enzymes in MucopolysaccharidosesEuropean Journal of Biochemistry, 1968
- Familial neurovisceral lipidosisThe Journal of Pediatrics, 1967
- Mutant Enzymatic and Cytological Phenotypes in Cultured Human FibroblastsScience, 1967
- HURLER'S SYNDROMEThe Journal of Experimental Medicine, 1966
- ULTRASTKUCTURAL AND BIOCHEMICAL OBSERVATIONS ON A CASE OF SYSTEMIC LATE INFANTILE LIPIDOSIS AND ITS RELATIONSHIP TO TAY-SACHS DISEASE AND GARGOYLISMJournal of Neuropathology and Experimental Neurology, 1965
- ELECTRON MICROSCOPY OF TWO CEREBRAL, BIOPSIES IN GARGOYLISMJournal of Neuropathology and Experimental Neurology, 1965
- Differential staining of acid glycosaminoglycans (mucopolysaccharides) by Alcian blue in salt solutionsHistochemistry and Cell Biology, 1965
- THE HISTOCHEMICAL DEMONSTRATION OF HISTAMINE IN MAST CELLSJournal of Histochemistry & Cytochemistry, 1961