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1 Ergebnisse
1
Manejo médico de pacientes con hemofilia A,B y enfermedad d..:
Peña Castellanos, Ángela María
;
Solano Trujillo, María Helena
;
Villamizar Gómez, Licet
Sans-Sabrafen J, Besses-Raebel C, Vives-Corrons J. Coagulopatías plasmáticas congénitas. In: Elsevier, editor. Hematología clínica. 5a. edición Madrid. 2006;725-44. 2. Lichtman M, Beutler E, J(jpps T. Seligsohn U, Kaushanshy K,Prchal J. Williams Hematology. 7a. edición. 2006. 3. Mariani G, Konk.le B, lngerslev J. Congenital factor VIl deficiency: therapy with recombinan! activated factor Vll-a critica! appraisal. Hemophi!ia. 2006;12:19-27. 4. Lapecorella M,Mariani G. Factor VII deficiency: defining the clinical picture and optimizing therapeutic options. Haemophilia 2008; 1 4:1170-5. 5. lngerslev J, Hvad J. Surgery in Hemophilia. The general view: Patient selection, liming and preoperative assessment. Semin Hematol. 2006;43(Suppl 1):23-6. 6. Rickard K. Guidelines for therapy and optima! dosages of coagulation factors for treatment of bleeding and surgery in haemophilia. Haemophilia. 1995;1(Suppl. 1):8-13. 7. FederaciónMundial de Hemo.... , 2022
Link:
https://doi.org/10.31260/RepertMedCir.v20.n4.2011.779
RT Journal T1
Manejo médico de pacientes con hemofilia A,B y enfermedad de Von Willebrand llevados a cirugía al Hospital San José, Bogotá: 16 años de experiencia ; Medical management of patients with hemophilia A, B and Von Willebrand disease who underwent surgery a sixteen year experience at Hospital de San José, Bogotá
UL https://suche.suub.uni-bremen.de/peid=base-ftfucsalud:oai:repositorio.fucsalud.edu.co:001_2802&Exemplar=1&LAN=DE A1 Peña Castellanos, Ángela María A1 Solano Trujillo, María Helena A1 Villamizar Gómez, Licet PB Sociedad de Cirugía de Bogotá, Hospital de San José y Fundación Universitaria de Ciencias de la Salud YR 2022 K1 hemofilia K1 enfermedad de von Willebrand K1 cirugía K1 hemophilia K1 von Willebrand disease K1 surgery JF Sans-Sabrafen J, Besses-Raebel C, Vives-Corrons J. Coagulopatías plasmáticas congénitas. In: Elsevier, editor. Hematología clínica. 5a. edición Madrid. 2006;725-44. 2. Lichtman M, Beutler E, J(jpps T. Seligsohn U, Kaushanshy K,Prchal J. Williams Hematology. 7a. edición. 2006. 3. Mariani G, Konk.le B, lngerslev J. Congenital factor VIl deficiency: therapy with recombinan! activated factor Vll-a critica! appraisal. Hemophi!ia. 2006;12:19-27. 4. Lapecorella M,Mariani G. Factor VII deficiency: defining the clinical picture and optimizing therapeutic options. Haemophilia 2008; 1 4:1170-5. 5. lngerslev J, Hvad J. Surgery in Hemophilia. The general view: Patient selection, liming and preoperative assessment. Semin Hematol. 2006;43(Suppl 1):23-6. 6. Rickard K. Guidelines for therapy and optima! dosages of coagulation factors for treatment of bleeding and surgery in haemophilia. Haemophilia. 1995;1(Suppl. 1):8-13. 7. FederaciónMundial de Hemo... LK http://dx.doi.org/https://doi.org/10.31260/RepertMedCir.v20.n4.2011.779 DO https://doi.org/10.31260/RepertMedCir.v20.n4.2011.779 SF ELIB - SuUB Bremen
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