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3. Effect of mannose chain length on targeting of glucocerebrosidase for enzyme replacement therapy of Gaucher disease. Van Patten SM, Hughes H, Huff MR, Piepenhagen PA, Waire J, Qiu H, Ganesa C, Reczek D, Ward PV, Kutzko JP, Edmunds T. Glycobiology; 2007 May; 17(5):467-78. PubMed ID: 17251309 [Abstract] [Full Text] [Related]
4. Molecular biology of glucocerebrosidase and the treatment of Gaucher disease. Barranger JA, Tomich J, Weiler S, Sakallah S, Sansieri C, Mifflin T, Bahnson A, Wei FS, Wei JF, Vallor M. Cytokines Mol Ther; 1995 Sep; 1(3):149-63. PubMed ID: 9384672 [Abstract] [Full Text] [Related]
5. Enzyme replacement therapy in type I Gaucher disease. Kay AC, Saven A, Garver P, Thurston DW, Rosenbloom BF, Beutler E. Trans Assoc Am Physicians; 1991 Sep; 104():258-64. PubMed ID: 1845151 [No Abstract] [Full Text] [Related]
6. Comparative efficacy of dose regimens in enzyme replacement therapy of type I Gaucher disease. Altarescu G, Schiffmann R, Parker CC, Moore DF, Kreps C, Brady RO, Barton NW. Blood Cells Mol Dis; 2000 Aug; 26(4):285-90. PubMed ID: 11042029 [Abstract] [Full Text] [Related]
12. Velaglucerase alfa, a human recombinant glucocerebrosidase enzyme replacement therapy for type 1 Gaucher disease. Pastores GM. Curr Opin Investig Drugs; 2010 Apr 20; 11(4):472-8. PubMed ID: 20336596 [Abstract] [Full Text] [Related]
13. Enzyme Replacement Therapy in a Gaucher Family. Erdem N, Buran T, Berber I, Aydogdu I. J Natl Med Assoc; 2018 Aug 20; 110(4):330-333. PubMed ID: 30126557 [Abstract] [Full Text] [Related]
14. Gaucher disease: a century of delineation and research. Enzyme replacement therapy: model and clinical studies. Beutler E, Dale GL. Prog Clin Biol Res; 1982 Aug 20; 95():703-16. PubMed ID: 7122644 [Abstract] [Full Text] [Related]
15. Improvement of splenomegaly and pancytopenia by enzyme replacement therapy against type 1 Gaucher disease: a report of sibling cases. Tsuboi K, Iida S, Kato M, Hayami Y, Hanamura I, Miura K, Harada S, Komatsu H, Banno S, Wakita A, Nitta M, Ueda R. Int J Hematol; 2001 Apr 20; 73(3):356-62. PubMed ID: 11345203 [Abstract] [Full Text] [Related]
16. Replacement therapy for inherited enzyme deficiency--macrophage-targeted glucocerebrosidase for Gaucher's disease. Barton NW, Brady RO, Dambrosia JM, Di Bisceglie AM, Doppelt SH, Hill SC, Mankin HJ, Murray GJ, Parker RI, Argoff CE. N Engl J Med; 1991 May 23; 324(21):1464-70. PubMed ID: 2023606 [Abstract] [Full Text] [Related]
17. Enzyme replacement in Gaucher disease. Beutler E. PLoS Med; 2004 Nov 23; 1(2):e21. PubMed ID: 15578103 [Abstract] [Full Text] [Related]
20. [A retrospective study on enzyme replacement therapy in patients with Gaucher disease]. Duan YL, Zhang YH, Zang Y, Shi HP, Zhang WM, Hu YM. Zhonghua Er Ke Za Zhi; 2006 Sep 23; 44(9):653-6. PubMed ID: 17217655 [Abstract] [Full Text] [Related] Page: [Next] [New Search]