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Journal Abstract Search

250 related items for PubMed ID: 29471850

  • 1. Taliglucerase alfa: safety and efficacy across 6 clinical studies in adults and children with Gaucher disease.
    Zimran A, Wajnrajch M, Hernandez B, Pastores GM.
    Orphanet J Rare Dis; 2018 Feb 23; 13(1):36. PubMed ID: 29471850
    [Abstract] [Full Text] [Related]

  • 2. Long-term safety and efficacy of taliglucerase alfa in pediatric Gaucher disease patients who were treatment-naïve or previously treated with imiglucerase.
    Zimran A, Gonzalez-Rodriguez DE, Abrahamov A, Cooper PA, Varughese S, Giraldo P, Petakov M, Tan ES, Chertkoff R.
    Blood Cells Mol Dis; 2018 Feb 23; 68():163-172. PubMed ID: 27839981
    [Abstract] [Full Text] [Related]

  • 3. A Phase 3, multicenter, open-label, switchover trial to assess the safety and efficacy of taliglucerase alfa, a plant cell-expressed recombinant human glucocerebrosidase, in adult and pediatric patients with Gaucher disease previously treated with imiglucerase.
    Pastores GM, Petakov M, Giraldo P, Rosenbaum H, Szer J, Deegan PB, Amato DJ, Mengel E, Tan ES, Chertkoff R, Brill-Almon E, Zimran A.
    Blood Cells Mol Dis; 2014 Dec 23; 53(4):253-60. PubMed ID: 24950666
    [Abstract] [Full Text] [Related]

  • 4. Long-term efficacy and safety results of taliglucerase alfa through 5years in adult treatment-naïve patients with Gaucher disease.
    Zimran A, Durán G, Giraldo P, Rosenbaum H, Giona F, Petakov M, Terreros Muñoz E, Solorio-Meza SE, Cooper PA, Varughese S, Alon S, Chertkoff R.
    Blood Cells Mol Dis; 2019 Sep 23; 78():14-21. PubMed ID: 27499018
    [Abstract] [Full Text] [Related]

  • 5. Enzyme replacement therapy with taliglucerase alfa: 36-month safety and efficacy results in adult patients with Gaucher disease previously treated with imiglucerase.
    Pastores GM, Shankar SP, Petakov M, Giraldo P, Rosenbaum H, Amato DJ, Szer J, Chertkoff R, Brill-Almon E, Zimran A.
    Am J Hematol; 2016 Jul 23; 91(7):661-5. PubMed ID: 27102949
    [Abstract] [Full Text] [Related]

  • 6. Enzyme replacement and substrate reduction therapy for Gaucher disease.
    Shemesh E, Deroma L, Bembi B, Deegan P, Hollak C, Weinreb NJ, Cox TM.
    Cochrane Database Syst Rev; 2015 Mar 27; 2015(3):CD010324. PubMed ID: 25812601
    [Abstract] [Full Text] [Related]

  • 7. Safety and efficacy of two dose levels of taliglucerase alfa in pediatric patients with Gaucher disease.
    Zimran A, Gonzalez-Rodriguez DE, Abrahamov A, Elstein D, Paz A, Brill-Almon E, Chertkoff R.
    Blood Cells Mol Dis; 2015 Jan 27; 54(1):9-16. PubMed ID: 25453586
    [Abstract] [Full Text] [Related]

  • 8. 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 27; 91(7):656-60. PubMed ID: 27174694
    [Abstract] [Full Text] [Related]

  • 9. Open-label, expanded access study of taliglucerase alfa in patients with Gaucher disease requiring enzyme replacement therapy.
    Kuter DJ, Wajnrajch M, Hernandez B, Wang R, Chertkoff R, Zimran A.
    Blood Cells Mol Dis; 2020 May 27; 82():102418. PubMed ID: 32146279
    [Abstract] [Full Text] [Related]

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  • 12. Taliglucerase alfa in Gaucher disease: Description of a Brazilian experience.
    Cravo R, Rotman V, Oliveira PMN, Defendi HGT, Conceição DA, Xavier JR, Chertkoff R, Noronha TG, Maia MLS.
    Blood Cells Mol Dis; 2018 Feb 27; 68():160-162. PubMed ID: 28131618
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  • 15. Pivotal trial with plant cell-expressed recombinant glucocerebrosidase, taliglucerase alfa, a novel enzyme replacement therapy for Gaucher disease.
    Zimran A, Brill-Almon E, Chertkoff R, Petakov M, Blanco-Favela F, Muñoz ET, Solorio-Meza SE, Amato D, Duran G, Giona F, Heitner R, Rosenbaum H, Giraldo P, Mehta A, Park G, Phillips M, Elstein D, Altarescu G, Szleifer M, Hashmueli S, Aviezer D.
    Blood; 2011 Nov 24; 118(22):5767-73. PubMed ID: 21900191
    [Abstract] [Full Text] [Related]

  • 16. Safety and efficacy results of switch from imiglucerase to velaglucerase alfa treatment in patients with type 1 Gaucher disease.
    Elstein D, Mehta A, Hughes DA, Giraldo P, Charrow J, Smith L, Shankar SP, Hangartner TN, Kunes Y, Wang N, Crombez E, Zimran A.
    Am J Hematol; 2015 Jul 24; 90(7):592-7. PubMed ID: 25776130
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  • 18. Spotlight on taliglucerase alfa in the treatment of pediatric patients with type 1 Gaucher disease.
    Gupta P, Pastores GM.
    Pediatric Health Med Ther; 2017 Jul 24; 8():73-81. PubMed ID: 29388611
    [Abstract] [Full Text] [Related]

  • 19. Pharmacokinetics of Novel Plant Cell-Expressed Taliglucerase Alfa in Adult and Pediatric Patients with Gaucher Disease.
    Abbas R, Park G, Damle B, Chertkoff R, Alon S.
    PLoS One; 2015 Jul 24; 10(6):e0128986. PubMed ID: 26053270
    [Abstract] [Full Text] [Related]

  • 20. Improvement in bone marrow infiltration in patients with type I Gaucher disease treated with taliglucerase alfa.
    Zimran A, Dinur T, Revel-Vilk S, Akkerman EM, van Dussen L, Hollak CEM, Maayan H, Altarescu G, Chertkoff R, Maas M.
    J Inherit Metab Dis; 2018 Nov 24; 41(6):1259-1265. PubMed ID: 30066229
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