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24. Identification of Fabry's disease by the screening of alpha-galactosidase A activity in male and female hemodialysis patients. Tanaka M; Ohashi T; Kobayashi M; Eto Y; Miyamura N; Nishida K; Araki E; Itoh K; Matsushita K; Hara M; Kuwahara K; Nakano T; Yasumoto N; Nonoguchi H; Tomita K Clin Nephrol; 2005 Oct; 64(4):281-7. PubMed ID: 16240899 [TBL] [Abstract][Full Text] [Related]
25. 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; 142(2):257-61. PubMed ID: 6094040 [No Abstract] [Full Text] [Related]
30. [Substrate specificity of multiple forms of human alpha-D-galactosidase and alpha-D-fucosidase]. Baskaeva EM; Shono NI; Kozlova IK; Vidershaĭn GIa Biokhimiia; 1989 Mar; 54(3):421-6. PubMed ID: 2546612 [TBL] [Abstract][Full Text] [Related]
31. Detection of Fabry's disease carriers by enzyme assay of hair roots. Hatton CE; Cooper A; Sardharwalla IB J Inherit Metab Dis; 1989; 12 Suppl 2():369-71. PubMed ID: 2556612 [No Abstract] [Full Text] [Related]
32. ConA-mediated binding and uptake of purified alpha-galactosidase A in Fabry fibroblasts. Hasholt L; Sørensen SA Exp Cell Res; 1983 Oct; 148(2):405-11. PubMed ID: 6313412 [TBL] [Abstract][Full Text] [Related]
33. Neurological presentation of Fabry's disease in a 52 year old man. Mohanraj R; Leach JP; Broome JC; Smith DF J Neurol Neurosurg Psychiatry; 2002 Sep; 73(3):340-2. PubMed ID: 12185177 [TBL] [Abstract][Full Text] [Related]
34. [Angiokeratoma corporis diffusum (Fabry's disease). Update. Apropos of 2 cases]. Larralde de Luna M; García Díaz R; Sánchez G; Ilari R; Pierini AM; Campoy C; Chamoles NH Med Cutan Ibero Lat Am; 1985; 13(2):129-40. PubMed ID: 2995736 [TBL] [Abstract][Full Text] [Related]
35. Uptake of lysosomal enzymes by human fibroblasts: lack of uptake of fungal or plant glycosidases in comparison with a mammalian enzyme. Dooley KC; Applegarth DA J Inherit Metab Dis; 1980; 3(4):145-7. PubMed ID: 6787335 [TBL] [Abstract][Full Text] [Related]
36. Megadolichobasilar anomaly with thrombosis in a family with Fabry's disease and a novel mutation in the alpha-galactosidase A gene. Garzuly F; Maródi L; Erdös M; Grubits J; Varga Z; Gelpi E; Rohonyi B; Mázló M; Molnár A; Budka H Brain; 2005 Sep; 128(Pt 9):2078-83. PubMed ID: 15947062 [TBL] [Abstract][Full Text] [Related]
37. Fabry's disease: differentiation between two forms of -galactosidase by myoinositol. Crawhall JC; Banfalvi M Science; 1972 Aug; 177(4048):527-8. PubMed ID: 5050485 [TBL] [Abstract][Full Text] [Related]
38. Enzyme replacement therapy in patients with Fabry's disease. Tsuboi K J Int Med Res; 2007; 35(4):574-81. PubMed ID: 17697536 [TBL] [Abstract][Full Text] [Related]
39. [Efficacy of replacement enzyme therapy on central nervous system manifestations in Fabry's disease]. Besson G; Vadot W; Guellerin J Rev Med Interne; 2010 Dec; 31 Suppl 2():S257-9. PubMed ID: 21211675 [TBL] [Abstract][Full Text] [Related]
40. Molecular genetic, biochemical, and clinical studies in three families with cardiac Fabry's disease. Yoshitama T; Nakao S; Takenaka T; Teraguchi H; Sasaki T; Kodama C; Tanaka A; Kisanuki A; Tei C Am J Cardiol; 2001 Jan; 87(1):71-5. PubMed ID: 11137837 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]