40 results on '"Kint J"'
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2. Effect of Bacterial Neuraminidase on the Isoenzymes of Acid Hydrolases of Human Brain and Liver
3. Fabry's Disease: Alpha-Galactosidase Deficiency
4. Brain sphingolipids in I cell disease (mucolipidosis II).
5. ARGININOSUCCINIC ACIDURIA.
6. The GM1 Gangliosidosis (Landing Disease).
7. Le Plasma Suroxalate, Reactif de la Coagulation du Sang
8. In vitro restoration of deficient β-galactosidase activity in liver of patients with Hurler and Hunter disease
9. The GM1 Gangliosidosis (Landing Disease)
10. The Enzyme Defect in Fabry's Disease
11. A new thin-layer method for phenolic substances and coumarins
12. DEFICIENT ARGININOSUCCINASE ACTIVITY IN BRAIN IN ARGININOSUCCINICACIDURIA
13. [Effect of mucopolysaccharides on the solubility of lysosomal enzymes].
14. [Stoichiometric binding of concanavalin A to hydrolases of human serum and liver].
15. Glucosylceramide in plasma of patients with Niemann-Pick disease.
16. In vitro restoration of deficient beta-galactosidase activity in liver of patients with Hurler and Hunter disease.
17. Abnormal distribution of lysosomal isoenzymes in mucopolysaccharidosis.
18. Argininosuccinic aciduria. Neonatal variant with rapid fatal course.
19. [A simple system for gradient-electrofocusing on small columns].
20. GM1-ganglioside accumulation and beta-galactosidase deficiency in a case of GM1-gangliosidosis (Landing disease).
21. [Type II mucolipidosis (I-cell disease)].
22. [FETAL ERYTHROCYTES IN PREGNANT, PUERPERAL AND NORMAL BELGIAN WOMEN].
23. Abnormal distribution patterns of lysosomal isoenzymes in mucopolysaccharidosis.
24. ABO blood groups and lysosomal diseases.
25. Type-II GM-1 gangliosidosis?
26. [Apropos of 2 cases of feto-maternal hemorrhage demonstrated by the presence of fetal erythrocytes in the blood of the mother].
27. New evidence for the identity of homoserine deaminase and cystathionase in human liver.
28. The biochemical abnormalities in Fabry's disease.
29. Beta-galactosidase activity in human leukocytes.
30. Histidinemia.
31. [Mucolipidosis of type II (I-cell disease): study of 3 cases].
32. On the existence and the enzymic interconversion of the isozymes of alpha-galactosidase in human organs.
33. Antagonistic action of chondroitin sulphate and cetylpyridinium chloride on human liver beta-galactosidase.
34. The formation of o-coumaroyl-beta-glucoside from coumarin-2-14C in barley embryos.
35. [Biochemistry of Fabry's disease].
36. A new thin-layer chromatography of phenolic acids and coumarins.
37. GM1 gangliosidosis type II.
38. [Enzymatic aspects of sphingolipoidosis].
39. Interactions between acid hydrolases of human liver and mucopolysaccharides.
40. Niemann-Pick disease.
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