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25. [Molecular genetics of inherited metabolic diseases--its application to the investigation of pathogenesis and the diagnosis of Fabry disease]. Sakuraba H Rinsho Byori; 1994 Jun; 42(6):628-35. PubMed ID: 7914243 [TBL] [Abstract][Full Text] [Related]
26. Letter: Diagnosis of Fabry's disease by tear alpha-galactosidase A. Del Monte MA; Johnson DL; Cotlier E; Krivit W; Desnick RJ N Engl J Med; 1974 Jan; 290(1):57-8. PubMed ID: 4202326 [No Abstract] [Full Text] [Related]
27. In vitro study of encapsulation therapy for Fabry disease using genetically engineered CHO cell line. Naganawa Y; Ohsugi K; Kase R; Date I; Sakuraba H; Sakuragawa N Cell Transplant; 2002; 11(4):325-9. PubMed ID: 12162373 [TBL] [Abstract][Full Text] [Related]
29. Later-onset Fabry disease: an adult variant presenting with the cramp-fasciculation syndrome. Nance CS; Klein CJ; Banikazemi M; Dikman SH; Phelps RG; McArthur JC; Rodriguez M; Desnick RJ Arch Neurol; 2006 Mar; 63(3):453-7. PubMed ID: 16533976 [TBL] [Abstract][Full Text] [Related]
30. A successful approach for the detection of Fabry patients in Argentina. Rozenfeld PA; Tarabuso A; Ebner R; Ramallo G; Fossati CA Clin Genet; 2006 Apr; 69(4):344-8. PubMed ID: 16630168 [TBL] [Abstract][Full Text] [Related]
31. [Fabry disease: clinical, biochemical and electron microscopical studies (author's transl)]. Klug H; Zabel R; Evers U Dermatol Monatsschr; 1979 Jan; 165(1):46-54. PubMed ID: 220105 [TBL] [Abstract][Full Text] [Related]
32. [Anderson-Fabry disease]. Kes P; Basić-Jukić N; Brunetta B; Jurić I Acta Med Croatica; 2006; 60(1):55-8. PubMed ID: 16802573 [TBL] [Abstract][Full Text] [Related]
33. Direct comparison of enzyme measurements from dried blood and leukocytes from male and female Fabry disease patients. Lukacs Z; Hartung R; Beck M; Keil A; Mengel E J Inherit Metab Dis; 2007 Aug; 30(4):614. PubMed ID: 17694354 [TBL] [Abstract][Full Text] [Related]
34. Enzymatic corrections for cells derived from Fabry disease patients by a recombinant adenovirus vector. Ohsugi K; Kobayashi K; Itoh K; Sakuraba H; Sakuragawa N J Hum Genet; 2000; 45(1):1-5. PubMed ID: 10697955 [TBL] [Abstract][Full Text] [Related]
35. The use of conjunctival biopsy and enzyme analysis in tears for the diagnosis of homozygotes and heterozygotes with Fabry disease. Libert J; Tondeur M; Van Hoof F Birth Defects Orig Artic Ser; 1976; 12(3):221-39. PubMed ID: 821559 [TBL] [Abstract][Full Text] [Related]
36. Anderson-Fabry disease with cerebrovascular complications in two Italian families. Borsini W; Giuliacci G; Torricelli F; Pelo E; Martinelli F; Scordo MR Neurol Sci; 2002 Jun; 23(2):49-53. PubMed ID: 12235491 [TBL] [Abstract][Full Text] [Related]