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161 related items for PubMed ID: 21515249

  • 1. Whole-blood alpha-D-galactosidase A activity for the identification of Fabry's patients.
    Massaccesi L, Burlina A, Baquero CJ, Goi G, Burlina AP, Tettamanti G.
    Clin Biochem; 2011 Jul; 44(10-11):916-21. PubMed ID: 21515249
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  • 3. Enzymatic diagnosis of Fabry disease using a fluorometric assay on dried blood spots: An alternative methodology.
    Caudron E, Prognon P, Germain DP.
    Eur J Med Genet; 2015 Dec; 58(12):681-4. PubMed ID: 26520229
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  • 5. [Angiokeratoma corporis diffusum (Fabry's disease). Biochemical diagnosis in plasma].
    Atzpodien W, Kremer GJ, Schnellbacher E, Denk R, Haferkamp G, Bierbach H.
    Dtsch Med Wochenschr; 1975 Feb 28; 100(9):423-6. PubMed ID: 803896
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  • 7. 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 Feb 28; 2(1):9-12. PubMed ID: 6273649
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  • 9. Effect of sample collection on alpha-galactosidase A enzyme activity measurements in dried blood spots on filter paper.
    Olivova P, van der Veen K, Cullen E, Rose M, Zhang XK, Sims KB, Keutzer J, Browning MF.
    Clin Chim Acta; 2009 May 28; 403(1-2):159-62. PubMed ID: 19245803
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  • 12. 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 01; 87(1):71-5. PubMed ID: 11137837
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  • 15. [Early acroparesthesia in females: a sign disclosing heterozygote Fabry disease].
    Larrégue M, Trincal D, Bressieux JM, Fusade T, Tanzer J, Menguy C.
    Ann Dermatol Venereol; 1991 Jan 01; 118(3):191-7. PubMed ID: 1648327
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  • 16. A case of Fabry's disease.
    Miura M, Tomino Y, Inoue W, Endoh M, Suga T, Kaneshige H, Nomoto Y, Sakai H, Matsuo I, Nagura H, Ikeda N.
    Tokai J Exp Clin Med; 1983 Jan 01; 8(1):23-9. PubMed ID: 6310828
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  • 17. [Renal involvement in Fabry's disease: diagnosis, follow-up and enzyme replacement therapy].
    Mignani R, Feriozzi S, Carraro G, Martinelli F, Cianciaruso B.
    G Ital Nefrol; 2009 Jan 01; 26(5):577-84. PubMed ID: 19802803
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  • 18. High incidence of thrombosis in Fabry's disease.
    Utsumi K, Yamamoto N, Kase R, Takata T, Okumiya T, Saito H, Suzuki T, Uyama E, Sakuraba H.
    Intern Med; 1997 May 01; 36(5):327-9. PubMed ID: 9213168
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  • 20. 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 01; 128(Pt 9):2078-83. PubMed ID: 15947062
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