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Implantoprosthetic rehabilitation of a patient with severe form of hemophilia B: a case report

subcommittee of factor VIII and factor IX of the scientific and standarization committee of the International Society on Thrombosis and Haemostasis Thromb Haemost. 2001 85 560 [4] Lehmann-Kopydlowska M, Zawilska K. Dental guidelines in congenital hemophilia A and B. Czas Stomatol. 2010;63(6):345-357. Lehmann-Kopydlowska M Zawilska K. Dental guidelines in congenital hemophilia A and B Czas Stomatol. 2010 63 6 345 357 [5] Bjorkman S, Carlsson M, Berntop E. Pharmacokinetics of factor IX in patients with haemophilia B: Methodological aspects and physiological interpretation

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Progressive arthropathy in the course of immune tolerance induction failure in a child with hemophilia A and FVIII inhibitor – a case report

children with severe haemophilia A: a protocol from the UK Haemophilia Centre Doctors’ Organisation Inhibitor and Paediatric Working Parties. Haemophilia 2017;23:654–59. 28574205 10.1111/hae.13264 Collins P Chalmers E Alamelu J et al First-line immune tolerance induction for children with severe haemophilia A: a protocol from the UK Haemophilia Centre Doctors’ Organisation Inhibitor and Paediatric Working Parties Haemophilia 2017 23 654 59 [2] Ananyeva NM, Lacroix-Esmazes S, Hauser CA. Inhibitors in hemophilia A: mechanisms of inhibitor

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False-negative coagulation factor activity results due to the presence of antiphospholipid antibodies in a case of autoimmune hemolytic anemia

detection of immune responses to FVIII: a study of 246 samples and correlation with the Bethesda assay. Haemophilia 2007;13:317-322. 10.1111/j.1365-2516.2007.01450.x Sahud MA Pratt KP Zhukov O Qu K Thompson AR. ELISA system for detection of immune responses to FVIII. a study of 246 samples and correlation with the Bethesda assay Haemophilia 2007 13 317 322 [12] Tiede A, Werwitzke S, Scharf RE: Laboratory diagnosis of acquired hemophilia A: limitations, consequences, and challenges. Semin Thromb Hemost. 2014;40:803-811. 10.1055/s-0034-1390004 Tiede A Werwitzke S Scharf

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Terapia manualna po alloplastyce stawu kolanowego u pacjenta z artropatią hemofilową w przebiegu hemofilii A – studium przypadku

arthroplasty. Haemophilia 2011;17:999–1004. Viliani T Zambelan G Pandolfi C et al In‐patient rehabilitation in haemophilic subjects with total knee arthroplasty Haemophilia 2011 17 999 1004 [4] Stephensen D, Bladen M, McLaughlin P. Recent advances in musculoskeletal physiotherapy for haemophilia. Ther Adv Hematol 2018;9:227–37. 10.1177/2040620718784834 30181843 Stephensen D Bladen M McLaughlin P Recent advances in musculoskeletal physiotherapy for haemophilia Ther Adv Hematol 2018 9 227 37 [5] Jaworski JM, Zawojski A, Zdziarska J

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Abnormal hemostasis screening tests leading to diagnosis of multiple myeloma

typical for MM (84%). Complete blood count (CBC) abnormalities include normocytic anemia (ca 70%), rouleaux-forming erythrocytes (50%), leukopenia and thrombocytopenia (20% and 5%, respectively) [ 1 , 2 ]. It is known that plasma cell dyscrasias can be accompanied by both thrombotic and hemorrhagic events, including venous thrombosis, acquired von Willebrand syndrome and acquired hemophilia. Increased risk of venous thromboembolism in myeloma patients is associated with increased FVIII and von Willebrand factor activity [ 3 , 4 , 5 ], decreased protein S activity

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