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PUBMED FOR HANDHELDS

Journal Abstract Search

112 related items for PubMed ID: 219278

  • 1.
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  • 3. [Biochemical and pathological studies on a carrier of Fabry's disease manifesting bouts of pain in the extremities].
    Katayama M, Kobayashi T, Ohnishi A, Goto I, Kuroiwa Y.
    Rinsho Shinkeigaku; 1984 Jun; 24(6):575-80. PubMed ID: 6094070
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  • 4. Fibroblast alpha-galactosidase A activity for identification of Fabry's disease heterozygotes.
    Fensom AH, Benson PF, Grant AR, Jacobs L.
    J Inherit Metab Dis; 1980 Jun; 2(1):9-12. PubMed ID: 6273649
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  • 5. Molecular pathology of Fabry's disease. Physical and kinetic properties of alpha-galactosidase A in cultured human endothelial cells.
    Johnson DL, Desnick RJ.
    Biochim Biophys Acta; 1978 Jan 18; 538(2):195-204. PubMed ID: 23178
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  • 6. Differential assay for lysosomal alpha-galactosidases in human tissues and its application to Fabry's disease.
    Mayes JS, Scheerer JB, Sifers RN, Donaldson ML.
    Clin Chim Acta; 1981 May 05; 112(2):247-51. PubMed ID: 6263521
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  • 7. Relationship of the multiple forms of human alpha-D-galactosidase and alpha-D-fucosidase in the normal and in Fabry's disease.
    Beyer E, Schono N, Kozlova I, Wiederschain G.
    Biochim Biophys Acta; 1990 May 08; 1038(3):386-9. PubMed ID: 2160280
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  • 10. Fabry's disease: biochemical and histochemical studies on hair roots for carrier detection.
    Vermorken AJ, Weterings PJ, Spierenburg GT, vanBennekom CA, Wirtz P, deBruyn CH, Oei TL.
    Br J Dermatol; 1978 Feb 08; 98(2):191-6. PubMed ID: 204324
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  • 12. Detection of Fabry's disease heterozygotes by hair root analysis.
    Beaudet AL, Caskey CT.
    Clin Genet; 1978 Mar 08; 13(3):251-8. PubMed ID: 205381
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  • 13. The fate of internalized alpha-2-macroglobulin: alpha-galactosidase conjugate in fibroblasts from Fabry's hemizygote.
    Osada T, Kuroda Y, Ikai A.
    Biochem Biophys Res Commun; 1987 Mar 30; 143(3):954-8. PubMed ID: 2436620
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  • 14. On the diagnosis of Fabry's disease.
    Wadskov S, Andersen V, Kobayasi T, Søondergaard J, Søorensen SA.
    Acta Derm Venereol; 1975 Mar 30; 55(5):363-6. PubMed ID: 52972
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  • 15. An atypical variant of Fabry's disease in men with left ventricular hypertrophy.
    Nakao S, Takenaka T, Maeda M, Kodama C, Tanaka A, Tahara M, Yoshida A, Kuriyama M, Hayashibe H, Sakuraba H.
    N Engl J Med; 1995 Aug 03; 333(5):288-93. PubMed ID: 7596372
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  • 16. [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 Aug 03; 13(2):129-40. PubMed ID: 2995736
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  • 17. 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 03; 128(Pt 9):2078-83. PubMed ID: 15947062
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  • 18. Clinical, histopathological, and biochemical findings in Fabry's disease. A case report and family study.
    Savi M, Olivetti G, Neri TM, Curtoni C.
    Arch Pathol Lab Med; 1977 Oct 03; 101(10):536-9. PubMed ID: 199133
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  • 19. Detection of Fabry's disease carriers by enzyme assay of hair roots.
    Hatton CE, Cooper A, Sardharwalla IB.
    J Inherit Metab Dis; 1989 Oct 03; 12 Suppl 2():369-71. PubMed ID: 2556612
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  • 20. Residual activity of alpha-galactosidase A in Fabry's disease.
    Romeo G, D'Urso M, Pisacane A, Blum E, De Falco A, Ruffilli A.
    Biochem Genet; 1975 Oct 03; 13(9-10):615-28. PubMed ID: 812485
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