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Journal Abstract Search

320 related items for PubMed ID: 18022018

  • 21. Clinical spectrum of Anderson Fabry disease in a Romanian family.
    Tudor A, Muşat A, Doscan A, Bari M, Zapucioiu C, Urdea E, Cochior D, Peţa D.
    Rom J Intern Med; 2006; 44(2):201-10. PubMed ID: 17236300
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  • 22. [Fabry's disease (alpha-galactosidase-A deficiency): recent therapeutic innovations].
    Germain DP.
    J Soc Biol; 2002; 196(2):183-90. PubMed ID: 12360747
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  • 24. 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
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  • 27. Hemizygous Fabry disease associated with IgA nephropathy: a case report.
    Shimohata H, Yoh K, Takada K, Tanaka H, Usui J, Hirayama K, Kobayashi M, Yamagata K.
    J Nephrol; 2009 Apr; 22(5):682-4. PubMed ID: 19810002
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  • 29. Preclinical efficacy and safety of 1-deoxygalactonojirimycin in mice for Fabry disease.
    Ishii S, Chang HH, Yoshioka H, Shimada T, Mannen K, Higuchi Y, Taguchi A, Fan JQ.
    J Pharmacol Exp Ther; 2009 Mar; 328(3):723-31. PubMed ID: 19106170
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  • 30. [Enzyme replacement therapy in Fabry's disease].
    Alvarez L, del Pozo C, Trigueros M, Sánchez L, Albero MD, López-Menchero R, Ortega E.
    Nefrologia; 2005 Mar; 25(3):322-7. PubMed ID: 16053014
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  • 32. The molecular defect leading to Fabry disease: structure of human alpha-galactosidase.
    Garman SC, Garboczi DN.
    J Mol Biol; 2004 Mar 19; 337(2):319-35. PubMed ID: 15003450
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  • 33. Transplantation: impact of pretransplant renal insufficiency.
    Bahirwani R, Campbell MS, Siropaides T, Markmann J, Olthoff K, Shaked A, Bloom RD, Reddy KR.
    Liver Transpl; 2008 May 19; 14(5):665-71. PubMed ID: 18433034
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  • 34. 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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  • 36. [Clinical courses of two male siblings on hemodialysis for Fabry disease ].
    Itoh K, Tanaka M, Matsushita K, Miyamura N, Nishida K, Araki E, Nonoguchi H, Tomita K.
    Nihon Jinzo Gakkai Shi; 2005 Jul 01; 47(2):121-7. PubMed ID: 15859134
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  • 37. Enzyme replacement therapy for Fabry disease: morphologic and histochemical changes in the urinary sediments.
    Utsumi K, Mitsuhashi F, Asahi K, Sakurazawa M, Arii K, Komaba Y, Katsumata T, Katsura K, Kase R, Katayama Y.
    Clin Chim Acta; 2005 Oct 01; 360(1-2):103-7. PubMed ID: 16112661
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  • 38. Accelerated transport and maturation of lysosomal alpha-galactosidase A in Fabry lymphoblasts by an enzyme inhibitor.
    Fan JQ, Ishii S, Asano N, Suzuki Y.
    Nat Med; 1999 Jan 01; 5(1):112-5. PubMed ID: 9883849
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  • 39. Remarkable variability in renal disease in a large Slovenian family with Fabry disease.
    Verovnik F, Benko D, Vujkovac B, Linthorst GE.
    Eur J Hum Genet; 2004 Aug 01; 12(8):678-81. PubMed ID: 15162124
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