Phenotype–genotype correlations in hemophilia A carriers are consistent with the binary role of the phase between F8 and X‐chromosome inactivation von Radic, C. P., Rossetti, L. C., Abelleyro, M. M., Tetzlaff, T., Candela, M., Neme, D., Sciuccati, G., Bonduel, M., Medina‐Acosta, E., Larripa, I. B., Tezanos Pinto, M., De Brasi, C. D.

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PB1945: CLINICAL AND MOLECULAR CHARACTERISTICS OF CHILDREN WITH DIAMOND‐BLACKFAN ANEMIA (DBA): A SINGLE CENTER EXPERIENCE IN ARGENTINA von Mininni, M. F., Albero, A., Avalos, V. J., Cervio, C., Candás, A. C., Diaz, L., Chaves, D. A., Milanesio, B., Pepe, C. M., Sciuccati, G.

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Platelet aggregation and adenosine triphosphate release values in children and adults von BONDUEL, M., FRONTROTH, J. P., HEPNER, M., SCIUCCATI, G., FELIÚ‐TORRES, A.

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PB0288 Antiphospholipid Syndrome in Children: 30 Years Single-Center Prospective Pediatric Cohort from Argentina von Cervio, C., Annetta, E., Bianco, B., Sueldo, E., Frontroth, J., Hepner, M., Sciuccati, G.

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PB0668 Emicizumab Treatment Regimen Based on Vial Size Along with Quantification of Emicizumab Plasma Concentration. Real-World Experience from a Single Pediatric Center in Argenti... von Sciuccati, G., Sueldo, R., Cervio, C., Bianco, M., Frontroth, J., Annetta, S., Hepner, M.

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PB0856 Time Course of Thrombocytopenia during DDAVP Test in a Boy with a De Novo c.4121G>A ( p.Arg1374His) Variant of the VWF Gene von Frontroth, J., Hepner, M., Pepe, C., Chaves, A., Annetta, S., Sueldo, R., Cervio, C., Bianco, B., Sciuccati, G.

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Acenocoumarol therapy in pediatric patients von Bonduel, M., Sciuccati, G., Hepner, M., Torres, A.Feliu, Pieroni, G., Frontroth, J. P., Serviddio, R. M.

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Repeat course of rabbit antithymocyte globulin as salvage following initial therapy with rabbit antithymocyte globulin in acquired aplastic anemia von Clé, Diego V, Atta, Elias H, Dias, Danielle S P, Lima, Carlos B L, Bonduel, Mariana, Sciuccati, Gabriela, Medeiros, Larissa A, de Oliveira, Michel M, Salvino, Marco A, Garanito, Marlene, Saad, Sara T Ollala, Calado, Rodrigo T, Scheinberg, Phillip

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The complex genetic landscape of familial MDS and AML reveals pathogenic germline variants von Rio-Machin, A, Vulliamy, T, Hug, N, Walne, A, Tawana, K, Cardoso, S, Ellison, A, Pontikos, N, Wang, J, Tummala, H, Al Seraihi, AFH, Alnajar, J, Bewicke-Copley, F, Armes, H, Barnett, M, Bloor, A, Bodor, C, Bowen, D, Fenaux, P, Green, A, Hallahan, A, Hjorth-Hansen, H, Hossain, U, Killick, S, Lawson, S, Layton, M, Male, AM, Marsh, J, Mehta, P, Mous, R, Nomdedeu, JF, Owen, C, Pavlu, J, Payne, EM, Protheroe, RE, Preudhomme, C, Pujol-Moix, N, Renneville, A, Russell, N, Saggar, A, Sciuccati, G, Taussig, D, Toze, CL, Uyttebroeck, A, Vandenberghe, P, Schlegelberger, B, Ripperger, T, Steinemann, D, Wu, J, Mason, J, Page, P, Akiki, S, Reay, K, Cavenagh, JD, Plagnol, V, Caceres, JF, Fitzgibbon, J, Dokal, I

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Prospective study of low-dose ristocetin-induced platelet aggregation to identify type 2B von Willebrand disease (VWD) and platelet-type VWD in children von Frontroth, Juan Pablo, Hepner, Mirta, Sciuccati, Gabriela, Torres, Aurora Feliú, Pieroni, Graciela, Bonduel, Mariana

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Validación de un método para la cuantificación plasmática de emicizumab von Sueldo, R.E, Hepner, M, Annetta, E, Cervio, C, Sciuccati, G, Frontroth, J.P, Bianco, B

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Validación de un método para la cuantificación plasmática de emicizumab von Sueldo, RE, Annetta, E, Frontroth, JP, Cervio, C, Bianco, B, Sciuccati, G, Hepner, M

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Prothrombotic disorders in children with Moyamoya syndrome von BONDUEL, Mariana, HEPNER, Mirta, SCIUCCATI, FELIU TORRES, Aurora, TENEMBAUM, Silvia

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Recurrent activating STAT5B N642H mutation in myeloid neoplasms with eosinophilia von Cross, NCP, Hoade, Y, Tapper, WJ, Carreno-Tarragona, G, Fanelli, T, Jawhar, M, Naumann, N, Pieniak, I, Lübke, J, Ali, S, Bhuller, K, Burgstaller, S, Cargo, C, Cavenagh, J, Duncombe, AS, Das-Gupta, E, Evans, P, Forsyth, P, George, P, Grimley, C, Jack, F, Munro, L, Mehra, V, Patel, K, Rismani, A, Sciuccati, G, Thomas-Dewing, R, Thornton, P, Virchis, A, Watt, S, Wallis, L, Whiteway, A, Zegocki, K, Bain, BJ, Reiter, A, Chase, A

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Factor V leiden and prothrombin gene G20210A mutation in children with cerebral thromboembolism von Bonduel, Mariana, Sciuccati, Gabriela, Hepner, Mirta, Pieroni, Graciela, Torres, Aurora Feliú, Mardaraz, Claudia, Frontroth, Juan Pablo

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Arterial Ischemic Stroke and Cerebral Venous Thrombosis in Children: A 12-Year Argentinean Registry von Bonduel, Mariana, Sciuccati, Gabriela, Hepner, Mirta, Pieroni, Graciela, Torres, Aurora Feliú, Frontroth, Juan Pablo, Tenembaum, Silvia

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Factor V Leiden and Prothrombin Gene G20210A Mutation in Children with Venous Thromboembolism von Bonduel, Mariana, Hepner, Mirta, Sciuccati, Gabriela, Pieroni, Graciela, Feliú-Torres, Aurora, Mardaraz, Claudia, Frontroth, Juan Pablo

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Hemoglobin San Martin: A New Unstable Variant Associated with Hemoglobin S in an Argentinean Boy von Feliu-Torres, Aurora, Eandi-Eberle, S., Calvo, K., Bragós, I., Ojeda, M., Voss, M., Pratti, A., Milani, A., Targovnik, H., Sciuccati, G., Bonduel, M., Diaz, L., Staciuk, R., Noguera, N.

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Prothrombotic abnormalities in children with venous thromboembolism von BONDUEL, M, HEPNER, M, SCIUCCATI, G, TORRES, A. F, PIERONI, G, FRONTROTH, J. P

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Familial idiopathic myelofibrosis and multiple hemangiomas von Bonduel, Mariana, Sciuccati, Gabriela, Torres, Aurora Feliú, Pierini, Adrián, Gallo, Guillermo

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