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PUBMED FOR HANDHELDS

Journal Abstract Search


274 related items for PubMed ID: 22047948

  • 21. Phase 1/2 and extension study of velaglucerase alfa replacement therapy in adults with type 1 Gaucher disease: 48-month experience.
    Zimran A, Altarescu G, Philips M, Attias D, Jmoudiak M, Deeb M, Wang N, Bhirangi K, Cohn GM, Elstein D.
    Blood; 2010 Jun 10; 115(23):4651-6. PubMed ID: 20299511
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  • 26. Long-term efficacy and safety results of taliglucerase alfa up to 36 months in adult treatment-naïve patients with Gaucher disease.
    Zimran A, Durán G, Mehta A, Giraldo P, Rosenbaum H, Giona F, Amato DJ, Petakov M, Muñoz ET, Solorio-Meza SE, Cooper PA, Varughese S, Chertkoff R, Brill-Almon E.
    Am J Hematol; 2016 Jul 10; 91(7):656-60. PubMed ID: 27174694
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  • 37. The budget impact of enzyme replacement therapy in type 1 Gaucher disease in the United States.
    Farahbakhshian S, Inocencio TJ, Poorman G, Wright E, Pathak RR, Bullano M.
    J Med Econ; 2022 Jul 10; 25(1):755-761. PubMed ID: 35611840
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  • 38. Evaluation of Spanish Gaucher disease patients after a 6-month imiglucerase shortage.
    Giraldo P, Irún P, Alfonso P, Dalmau J, Fernández-Galán MA, Figueredo A, Hernández-Rivas JM, Julia A, Luño E, Marín-Jimenez F, Martín-Nuñez G, Montserrat JL, de la Serna J, Vidaller A, Villalón L, Pocovi M.
    Blood Cells Mol Dis; 2011 Jan 15; 46(1):115-8. PubMed ID: 20934891
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  • 40. Treatment-naïve Gaucher disease patients achieve therapeutic goals and normalization with velaglucerase alfa by 4years in phase 3 trials.
    Zimran A, Elstein D, Gonzalez DE, Lukina EA, Qin Y, Dinh Q, Turkia HB.
    Blood Cells Mol Dis; 2018 Feb 15; 68():153-159. PubMed ID: 27839979
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