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Journal Abstract Search
112 related items for PubMed ID: 219278
21. Properties of immobilized fig alpha-galactosidase and effect on ceramide-3 content of plasma from patients with Fabry's disease. Schram AW, Hamers MN, Oldenbroek-Haverkamp E, Strijland A, de Jonge A, van den Bergh FA, Tager JM. Biochim Biophys Acta; 1978 Dec 08; 527(2):456-64. PubMed ID: 31916 [Abstract] [Full Text] [Related]
23. [Fabry's disease. An orphan disease that has found a solution: enzymatic replacement with alpha-galactosidase]. Selgas R, García de Lorenzo A, Valdés F, Beck M. Nefrologia; 2001 Apr 08; 21(5):443-7. PubMed ID: 11795012 [No Abstract] [Full Text] [Related]
28. The properties of alpha-galactosidase remaining in kidney and liver of patients with Fabry's disease. Kano I, Yamakawa T. Chem Phys Lipids; 1974 Dec 08; 13(4):283-91. PubMed ID: 4217662 [No Abstract] [Full Text] [Related]
35. New therapies for Fabry's disease. Gahl WA. N Engl J Med; 2001 Jul 05; 345(1):55-7. PubMed ID: 11439950 [No Abstract] [Full Text] [Related]
36. [Fabry's disease: kidney insufficiency in heterozygous patient]. Pravatà G, Pinto G, Noto G, Aricò M. G Ital Dermatol Venereol; 1989 Jul 05; 124(11-12):505-9. PubMed ID: 2561653 [Abstract] [Full Text] [Related]
37. A case of Fabry's disease in a patient with no alpha-galactosidase A activity caused by a single amino acid substitution of Pro-40 by Ser. Koide T, Ishiura M, Iwai K, Inoue M, Kaneda Y, Okada Y, Uchida T. FEBS Lett; 1990 Jan 01; 259(2):353-6. PubMed ID: 2152885 [Abstract] [Full Text] [Related]
38. A microtechnique for quantitative measurements of acid hydrolases in fibroblasts. Its application in diagnosis of Fabry disease and enzyme replacement studies. Hasholt L, Sørensen SA. Clin Chim Acta; 1984 Sep 29; 142(2):257-61. PubMed ID: 6094040 [No Abstract] [Full Text] [Related]