Medical progress: Immune thrombocytopenic purpura von CINES, Douglas B, BLANCHETTE, Victor S

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The management of alloimmune neonatal thrombocytopenia von Blanchette, V.S., Johnson, J., Rand, M.

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Idiopathic thrombocytopenic purpura : A practice guideline developed by explicit methods for the American Society of Hematology von GEORGE, J. N, WOOLF, S. H, LICHTIN, A. E, MCMILLAN, R, OKERBLOOM, J. A, REGAN, D. H, WARRIER, I, RASKOB, G. E, WASSER, J. S, ALEDORT, L. M, BALLEM, P. J, BLANCHETTE, V. S, BUSSEL, J. B, CINES, D. B, KELTON, J. G

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The genetics of Canadian type 3 von Willebrand disease: further evidence for co‐dominant inheritance of mutant alleles von Bowman, M., Tuttle, A., Notley, C., Brown, C., Tinlin, S., Deforest, M., Leggo, J., Blanchette, V.S., Lillicrap, D., James, P.

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Tailored prophylaxis in severe hemophilia A: interim results from the first 5 years of the Canadian Hemophilia Primary Prophylaxis Study von FELDMAN, B. M., PAI, M., RIVARD, G. E., ISRAELS, S., POON, M.‐C., DEMERS, C., ROBINSON, S., LUKE, K.‐H., WU, J. K. M., GILL, K., LILLICRAP, D., BABYN, P., MCLIMONT, M., BLANCHETTE, V. S.

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Corticosteroids Versus Intravenous Immune Globulin for the Treatment of Acute Immune Thrombocytopenic Purpura in Children: A Systematic Review and Meta-Analysis of Randomized Contr... von Beck, Carolyn E., Nathan, Paul C., Parkin, Patricia C., Blanchette, Victor S., Macarthur, Colin

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Intensive exposure to factor VIII is a risk factor for inhibitor development in mild hemophilia A von Sharathkumar, A., Lillicrap, D., Blanchette, V. S., Kern, M., Leggo, J., Stain, A. M., Brooker, L., Carcao, M. D.

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Optimizing factor prophylaxis for the haemophilia population: where do we stand? von Blanchette, V. S., Manco-Johnson, M., Santagostino, E., Ljung, R.

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Rituximab for congenital haemophiliacs with inhibitors: a Canadian experience von CARCAO, M., ST LOUIS, J., POON, M-C., GRUNEBAUM, E., LACROIX, S., STAIN, A. M., BLANCHETTE, V. S., RIVARD, G. E.

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Consensus perspectives on prophylactic therapy for haemophilia: summary statement von Berntorp, E., Astermark, J., Björkman, S., Blanchette, V. S., Fischer, K., Giangrande, P. L. F., Gringeri, A., Ljung, R. C., Manco-Johnson, M. J., Morfini, M., Kilcoyne, R. F., Petrini, P., Rodriguez-Merchan, E. C., Schramm, W., Shapiro, A., M. Van Den Berg, H., Hart, C.

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The safety and efficacy of recombinant human blood coagulation factor IX in previously untreated patients with severe or moderately severe hemophilia B von Shapiro, Amy D., Paola, Jorge Di, Cohen, Alice, Pasi, K. John, Heisel, Margaret A., Blanchette, Victor S., Abshire, Thomas C., Hoots, W. Keith, Lusher, Jeanne M., Negrier, Claude, Rothschild, Chantal, Roth, David A.

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Prevention and treatment of musculoskeletal disease in the haemophilia population: role of prophylaxis and synovectomy von VAN DEN BERG, H. M., DUNN, A., FISCHER, K., BLANCHETTE, V. S.

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A prospective, longitudinal study of central venous catheter‐related deep venous thrombosis in boys with hemophilia von Price, V. E., Carcao, M., Connolly, B., Chait, P., Daneman, A., Temple, M., Stain, A. M., Sung, L., Al‐Tralbosi, H., Blanchette, V. S.

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Comparison of Plasma Exchange with Plasma Infusion in the Treatment of Thrombotic Thrombocytopenic Purpura von Rock, Gail A, Shumak, Kenneth H, Buskard, Noel A, Blanchette, Victor S, Kelton, John G, Nair, Rama C, Spasoff, Robert A

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Childhood Acute Immune Thrombocytopenic Purpura: 20 Years Later von Blanchette, Victor S., Carcao, Manuel

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The prevention and treatment of bacterial infections in children with asplenia or hyposplenia: Practice considerations at the Hospital for Sick Children, Toronto von Price, Victoria E., Dutta, Sanjeev, Blanchette, Victor S., Butchart, Sheila, Kirby, Melanie, Langer, Jacob C., Ford-Jones, E. Lee

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von Willebrand Disease in a Pediatric-based Population - Comparison of Type 1 Diagnostic Criteria and Use of the PFA-100 ® and a von Willebrand Factor/Collagen-binding Assay von Dean, J.A., Blanchette, V. S., Carcao, M. D., Stain, A. M., Sparling, C. R., Siekmann, J., Turecek, P. L., Lillicrap, D., Rand, M. L.

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Childhood chronic immune thrombocytopenic purpura: unresolved issues von Blanchette, Victor S, Price, Victoria

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Uncertain times for research on hemophilia and allied disorders von BLANCHETTE, V. S.

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Fcγ receptor IIa and IIIa polymorphisms in childhood immune thrombocytopenic purpura von Carcao, Manuel D., Blanchette, Victor S., Wakefield, Cindy D., Stephens, Derick, Ellis, Janet, Matheson, Kimberly, Denomme, Gregory A.

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