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Journal Abstract Search

487 related items for PubMed ID: 21675497

  • 1. Fabry disease.
    Tarabuso AL.
    Skinmed; 2011; 9(3):173-7. PubMed ID: 21675497
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  • 2. [Evaluation of patients with Fabry disease in Argentina].
    AADELFA (Asociación Argentina de estudio de enfermedad de Fabry y otras enfermedades lisosomales).
    Medicina (B Aires); 2010; 70(1):37-43. PubMed ID: 20228022
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  • 4. [Fabry disease].
    Jakubowska E, Ryba M, Hruby Z.
    Przegl Lek; 2006; 63(4):218-9. PubMed ID: 17080745
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  • 5. Fabry disease: treatment and diagnosis.
    Rozenfeld PA.
    IUBMB Life; 2009 Nov; 61(11):1043-50. PubMed ID: 19859978
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  • 6. Fabry disease: molecular genetics of the inherited nephropathy.
    Desnick RJ, Astrin KH, Bishop DF.
    Adv Nephrol Necker Hosp; 1989 Nov; 18():113-27. PubMed ID: 2564247
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  • 9. 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; 51(1):36-8. PubMed ID: 20148840
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  • 10. [Neurological complications of Fabry-disease].
    Vastagh I, Constantin T, Kéri A, Rudas G, Fekete G, Bereczki D.
    Ideggyogy Sz; 2011 Jan 30; 64(1-2):29-35. PubMed ID: 21428036
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  • 12. [Fabry disease: clinic and enzymatic diagnosis of homozygous and heterozygous. New therapeutic prospects].
    Peces R, Olea T.
    Nefrologia; 2002 Jan 30; 22(6):540-6. PubMed ID: 12516287
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  • 14. Correction of enzymatic and lysosomal storage defects in Fabry mice by adenovirus-mediated gene transfer.
    Ziegler RJ, Yew NS, Li C, Cherry M, Berthelette P, Romanczuk H, Ioannou YA, Zeidner KM, Desnick RJ, Cheng SH.
    Hum Gene Ther; 1999 Jul 01; 10(10):1667-82. PubMed ID: 10428212
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  • 20. Fabry disease: an ultrastructural comparative study of skin in hemizygous and heterozygous patients.
    Navarro C, Teijeira S, Dominguez C, Fernandez JM, Rivas E, Fachal C, Barrera S, Rodriguez C, Iranzo P.
    Acta Neuropathol; 2006 Feb 01; 111(2):178-85. PubMed ID: 16463201
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