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Hereditary factor XIII deficiency in children: diagnostic and clinical features and clinical experience with replacement therapy
Florinskiy D.B., Pshonkin A.V., Poletaev A.V., Seregina E.A., Zharkov P.A.
A clinical case of inhibitor development in a patient with type 3 von Willebrand disease and the use of emicizumab as hemostatic treatment
Florinskiy D.B., Pshonkin A.V., Yunusova I.M., Poletaev A.V., Seregina E.A., Sysoeva E.M., Zharkov P.A.
The prevalence of rare bleeding disorders among children in the Russian Federation
Zharkov P.A., Florinskiy D.B., Aleynikova O.V., Novichkovа G.A.
Immune tolerance induction with a high-purity von Willebrand factor containing plasma-derived factor VIII concentrate in a child with hemophilia A with inhibitors
Zharkov P.A., Fedorova D.V., Erega E.P., Poletaev A.V., Seregina E.A., Pshonkin A.V.
Congenital combined vitamin K-dependent clotting factors deficiency: case reports
Florinskiy D.B., Zharkov P.А., Pshonkin A.V., Poletaev A.V., Fedorova D.V., Seregina E.A.
The use of a spatial thrombin generation method for assessment of platelet procoagulant activity after platelet concentrate transfusion in children
Kol'tsova E.M., Balandina J.A., Demina I.A., Radygina S.A., Ataullakhanov F.I., Balashov D.N., Panteleev M.A.
Principles of diagnosis and treatment of hereditary angioedema (Review of literature)
Kuzmenko N.B., Dibirova S.A., Varlamova T.V., Raikina E.V., Viktorova E.A., Shcherbina A.Y.
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