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23. The carrier potential of liposomes in biology and medicine (second of two parts). Gregoriadis G N Engl J Med; 1976 Sep; 295(14):765-70. PubMed ID: 785256 [No Abstract] [Full Text] [Related]
24. [Neuroepidemiology of metabolism inborn errors: diseases of lysosomal origin]. Chabás A An Esp Pediatr; 1988 Sep; 29 Suppl 33():48-51. PubMed ID: 3074716 [No Abstract] [Full Text] [Related]
25. Inherited lysosomal storage diseases: an essay in comparative medicine. Jolly RD; Blakemore WF Vet Rec; 1973 Apr; 92(15):391-400. PubMed ID: 4578828 [No Abstract] [Full Text] [Related]
26. Activity of some lysosomal enzymes in Hurler's syndrome (type i mucopolysaccharidosis). Cichocki T; Kobielowa Z; Krzanowska-Dyras M Mater Med Pol; 1974; 6(3):188-92. PubMed ID: 4216729 [No Abstract] [Full Text] [Related]
27. Lysosomal acid hydrolases in health and disease. Bachhawat BK Neurol India; 1974 Dec; 22(4):169-83. PubMed ID: 4449578 [No Abstract] [Full Text] [Related]
28. Letter: Enzyme-carrier potential of liposomes in enzyme replacement therapy. Gregoriadis G N Engl J Med; 1975 Jan; 292(4):215. PubMed ID: 1109221 [No Abstract] [Full Text] [Related]
29. Animal models of human erythrocyte metabolic abnormalities. Smith JE Clin Haematol; 1981 Feb; 10(1):239-51. PubMed ID: 6111407 [No Abstract] [Full Text] [Related]
33. New trends in the treatment of inborn errors of metabolism: an overview. Frézal J; Munnich A; Ogier H; Weil D; Saudubray JM Prog Clin Biol Res; 1982; 103 Pt B():563-71. PubMed ID: 7163247 [No Abstract] [Full Text] [Related]
34. Experimental enzyme replacement in genetic and other disorders. Weissmann G Hosp Pract; 1976 Sep; 11(9):49-58. PubMed ID: 1071086 [TBL] [Abstract][Full Text] [Related]
35. Lysosomal enzymes may cross the blood-brain-barrier by pinocytosis: implications for enzyme replacement therapy. Baldo G; Giugliani R; Matte U Med Hypotheses; 2014 Apr; 82(4):478-80. PubMed ID: 24560457 [TBL] [Abstract][Full Text] [Related]
36. [lysosomes and storage disease]. Raivio K Duodecim; 1981; 97(2):51-5. PubMed ID: 7249962 [No Abstract] [Full Text] [Related]
37. A suspected lysosomal storage disease in Abyssinian cats. Part I: genetic, clinical and clinical pathological aspects. Bland van den Berg P; Baker MK; Lange AL J S Afr Vet Assoc; 1977 Oct; 48(3):195-9. PubMed ID: 599532 [TBL] [Abstract][Full Text] [Related]
38. [Congenital lysosomal diseases]. Romanowska-Gõrecka B Pol Arch Med Wewn; 1972 Apr; 48(4):425-9. PubMed ID: 4556749 [No Abstract] [Full Text] [Related]
39. Aptamer-based endocytosis of a lysosomal enzyme. Chen CH; Dellamaggiore KR; Ouellette CP; Sedano CD; Lizadjohry M; Chernis GA; Gonzales M; Baltasar FE; Fan AL; Myerowitz R; Neufeld EF Proc Natl Acad Sci U S A; 2008 Oct; 105(41):15908-13. PubMed ID: 18838694 [TBL] [Abstract][Full Text] [Related]