The miR-200c/141-ZEB2-TGFβ axis is aberrant in human T-cell prolymphocytic leukemia von Erkeland, Stefan J, Stavast, Christiaan J, Schilperoord-Vermeulen, Joyce, Dal Collo, Giada, Van de Werken, Harmen J G, Leon, Leticia G, Van Hoven-Beijen, Antoinette, Van Zuijen, Iris, Mueller, Yvonne M, Bindels, Eric M, De Ridder, Dick, Kappers-Klunne, Mies C, Van Lom, Kirsten, Van der Velden, Vincent H J, Langerak, Anton W

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PFA-100 monitoring of von Willebrand factor (VWF) responses to desmopressin (DDAVP) and factor VIII/VWF concentrate substitution in von Willebrand disease type 1 and 2 von Huub H. D. M. van Vliet, Mies C. Kappers-Klunne, Frank W. G. Leebeek, Jan J. Michiels

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Association of asymmetric dimethylarginine with sickle cell disease-related pulmonary hypertension von Landburg, Precious P, Teerlink, Tom, van Beers, Eduard J, Muskiet, Frits A J, Kappers-Klunne, Mies C, van Esser, Joost W J, Mac Gillavry, Melvin R, Biemond, Bart J, Brandjes, Dees P M, Duits, Ashley J, Schnog, John-John

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Large and Medium-Sized Pulmonary Artery Obstruction Does Not Play a Role of Primary Importance in the Etiology of Sickle-Cell Disease-Associated Pulmonary Hypertension von van Beers, Eduard J., van Eck-Smit, Berthe L.F., Mac Gillavry, Melvin R., van Tuijn, Charlotte F.J., van Esser, Joost W.J., Brandjes, Dees P.M., Kappers-Klunne, Mies C., Duits, Ashley J., Biemond, Bart J., Schnog, John-John B.

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In vitro studies, pharmacokinetic studies and clinical use of a high purity double virus inactivated FVIII/VWF concentrate (Immunate) in the treatment of von Willebrand disease von Ver Elst, Kristien M. M., van Vliet, Huub D. M., Kappers-Klunne, Mies C., Leebeek, Frank W. G.

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A new polyadenylation site mutation associated with a mild beta-thalassemia phenotype von Giordano, PC, Bouva, MJ, Van Delft, P, Akkerman, N, Kappers-Klunne, MC, Harteveld, CL

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A novel 7.9 kb deletion causing α+-thalassaemia in two independent families of Indian origin von HARTEVELD, Cornelis L, VAN DELFT, Peter, WIJERMANS, Pierre W, KAPPERS-KLUNNE, Mies C, WEEGENAAR, Jitske, LOSEKOOT, Monique, GIORDANO, Piero C

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The miR-200c/141-ZEB2-TGFb axis is aberrant in human T-cell prolymphocytic leukemia von Erkeland, Stefan J., Stavast, Christiaan J., Schilperoord-Vermeulen, Joyce, Dal Collo, Giada, van de Werken, Harmen J.G., Leon, Leticia G., van Hoven-Beijen, Antoinette, van Zuijen, Iris, Mueller, Yvonne M., Bindels, Eric M., de Ridder, Dick, Kappers-Klunne, Mies C., van Lom, Kirsten, van der Velden, Vincent H.J., Langerak, Anton W.

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PFA-100 monitoring of von Willebrand factor (VWF) responses to desmopressin (DDAVP) and factorVIII/VWF concentrate substitution in von willebrand disease type I and 2 von VAN VLIET, Huub H. D. M, KAPPERS-KLUNNE, Mies C, LEEBEEK, Frank W. G, MICHIELS, Jan J

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Myeloproliferative Disease in the Pathogenesis and Survival of Budd-Chiari Syndrome von Smalberg, Jasper H., Murad, Sarwa D., Braakman, Eric, Valk, Peter, Kappers-Klunne, Mies C., Janssen, Harry L., Leebeek, Frank W.G.

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A novel 7.9 kb deletion causing (alpha+)-thalassaemia in two independent families of Indian origin von Harteveld, Cornelis L, Peter van Delft, Wijermans, Pierre W, Kappers-Klunne, Mies C

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A novel 7·9 kb deletion causing α+‐thalassaemia in two independent families of Indian origin von Harteveld, Cornelis L., Van Delft, Peter, Wijermans, Pierre W., Kappers‐Klunne, Mies C., Weegenaar, Jitske, Losekoot, Monique, Giordano, Piero C.

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A new polyadenylation site mutation associated with a mild beta-thalassemia phenotype von Giordano, Piero C, Bouva, Marelle J, Van Delft, Peter, Akkerman, Nicole, Kappers-Klunne, Mies C, Harteveld, Cornelis L

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B-cell prolymphocytic leukemia: a specific subgroup of mantle cell lymphoma von van der Velden, Vincent H.J., Hoogeveen, Patricia G., de Ridder, Dick, Schindler-van der Struijk, Magdalena, van Zelm, Menno C., Sanders, Mathijs, Karsch, Dennis, Beverloo, H. Berna, Lam, King, Orfao, Alberto, Lugtenburg, Pieternella J., Böttcher, Sebastian, van Dongen, Jacques J.M., Langerak, Anton W., Kappers-Klunne, Mies, van Lom, Kirsten

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