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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

220 related items for PubMed ID: 37289594

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  • 4. Efanesoctocog Alfa Prophylaxis for Patients with Severe Hemophilia A.
    von Drygalski A, Chowdary P, Kulkarni R, Susen S, Konkle BA, Oldenburg J, Matino D, Klamroth R, Weyand AC, Jimenez-Yuste V, Nogami K, Poloskey S, Winding B, Willemze A, Knobe K, XTEND-1 Trial Group.
    N Engl J Med; 2023 Jan 26; 388(4):310-318. PubMed ID: 36720133
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  • 6. Efanesoctocog Alfa: First Approval.
    Keam SJ.
    Drugs; 2023 May 26; 83(7):633-638. PubMed ID: 37022666
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  • 8. Efanesoctocog alfa for hemophilia A: results from a phase 1 repeat-dose study.
    Lissitchkov T, Willemze A, Katragadda S, Rice K, Poloskey S, Benson C.
    Blood Adv; 2022 Feb 22; 6(4):1089-1094. PubMed ID: 34794179
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  • 9. Recombinant factor VIII Fc fusion protein: extended-interval dosing maintains low bleeding rates and correlates with von Willebrand factor levels.
    Shapiro AD, Ragni MV, Kulkarni R, Oldenberg J, Srivastava A, Quon DV, Pasi KJ, Hanabusa H, Pabinger I, Mahlangu J, Fogarty P, Lillicrap D, Kulke S, Potts J, Neelakantan S, Nestorov I, Li S, Dumont JA, Jiang H, Brennan A, Pierce GF.
    J Thromb Haemost; 2014 Nov 22; 12(11):1788-800. PubMed ID: 25196897
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  • 13. Plasma Clearance of Coagulation Factor VIII and Extension of Its Half-Life for the Therapy of Hemophilia A: A Critical Review of the Current State of Research and Practice.
    Sarafanov AG.
    Int J Mol Sci; 2023 May 11; 24(10):. PubMed ID: 37239930
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  • 14. BIVV001, a new class of factor VIII replacement for hemophilia A that is independent of von Willebrand factor in primates and mice.
    Seth Chhabra E, Liu T, Kulman J, Patarroyo-White S, Yang B, Lu Q, Drager D, Moore N, Liu J, Holthaus AM, Sommer JM, Ismail A, Rabinovich D, Liu Z, van der Flier A, Goodman A, Furcht C, Tie M, Carlage T, Mauldin R, Dobrowsky TM, Liu Z, Mercury O, Zhu L, Mei B, Schellenberger V, Jiang H, Pierce GF, Salas J, Peters R.
    Blood; 2020 Apr 23; 135(17):1484-1496. PubMed ID: 32078672
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  • 17. Coagulation factor VIII regulates von Willebrand factor homeostasis invivo.
    Cao W, Trask AR, Bignotti AI, George LA, Doshi BS, Sabatino DE, Yada N, Zheng L, Camire RM, Zheng XL.
    J Thromb Haemost; 2023 Dec 23; 21(12):3477-3489. PubMed ID: 37726033
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  • 18. Predicting the outcomes of using longer-acting prophylactic factor VIII to treat people with severe hemophilia A: a hypothetical decision analysis.
    Miners AH, Krishnan S, Pasi KJ.
    J Thromb Haemost; 2016 Nov 23; 14(11):2141-2147. PubMed ID: 27510890
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  • 20. Perspective - The case for zero bleeds and drug bioequivalence in the treatment of congenital hemophilia A in 2021.
    Di Minno A, Spadarella G, Esposito S, Mathew P, Di Minno G, Mannucci PM.
    Blood Rev; 2021 Nov 23; 50():100849. PubMed ID: 34024681
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