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Journal Abstract Search

366 related items for PubMed ID: 12516287

  • 1. [Fabry disease: clinic and enzymatic diagnosis of homozygous and heterozygous. New therapeutic prospects].
    Peces R, Olea T.
    Nefrologia; 2002; 22(6):540-6. PubMed ID: 12516287
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  • 2. Clinical features of and recent advances in therapy for Fabry disease.
    Brady RO, Schiffmann R.
    JAMA; 2000 Dec 06; 284(21):2771-5. PubMed ID: 11105184
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  • 4. Fabry disease: molecular genetics of the inherited nephropathy.
    Desnick RJ, Astrin KH, Bishop DF.
    Adv Nephrol Necker Hosp; 1989 Dec 06; 18():113-27. PubMed ID: 2564247
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  • 7. Kidney transplantation and enzyme alpha-galactosidase A therapy in patient with Fabry disease: a case report.
    Dziemianko I, Jezior D, Boratyńska M, Patrzałek D, Kuźniar J, Szyber P, Klinger M.
    Transplant Proc; 2007 Nov 06; 39(9):2925-7. PubMed ID: 18022018
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  • 11. Fabry disease: clinical spectrum and evidence-based enzyme replacement therapy.
    Desnick RJ, Banikazemi M.
    Nephrol Ther; 2006 Jan 06; 2 Suppl 2():S172-85. PubMed ID: 17373219
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  • 14. Renal involvement in Anderson-Fabry disease.
    Sessa A, Meroni M, Battini G, Righetti M, Maglio A, Tosoni A, Nebuloni M, Vago G, Giordano F.
    J Nephrol; 2003 Jan 06; 16(2):310-3. PubMed ID: 12774774
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  • 17. A case of multiple angiomas without any angiokeratomas in a female heterozygote with Fabry disease.
    Mirceva V, Hein R, Ring J, Möhrenschlager M.
    Australas J Dermatol; 2010 Feb 06; 51(1):36-8. PubMed ID: 20148840
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