Pasado, presente y futuro | 04 OCT 22


Epidemiología, fisiopatología, manifestaciones clínicas y manejo de la hemofilia
Autor/a: Omar Matuk-Villazon, Jonathan C. Roberts, Fernando F. Corrales-Medina Pediatr Rev (2021) 42 (12): 672683.
INDICE:  1. Texto principal | 2. Referencia bibliográfica
Referencia bibliográfica

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36.Manco-Johnson MJ, Abshire TC, Shapiro AD, et al. Prophylaxis versus episodic treatment to prevent joint disease in boys with severe hemophilia. N Engl J Med. 2007;357(6):535–544

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40.Armstrong EP, Malone DC, Krishnan S, Wessler MJ. Adherence to clotting factors among persons with hemophilia A or B. Hematology. 2015;20(3):148–153

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43.Roberts JC, Lattimore S, Recht M, et al. Goal Attainment Scaling for haemophilia (GAS-Hēm): testing the feasibility of a new patient-centric outcome measure in people with haemophilia. Haemophilia. 2018;24(4):e199–e206

44.Lissitchkov T, Hampton K, von Depka M, et al. Novel, human cell line-derived recombinant factor VIII (human-cl rhFVIII; Nuwiq (®)) in adults with severe haemophilia A: efficacy and safety. Haemophilia. 2016;22(2):225–231



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