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Model of care for individuals with rare cancer predisposition syndromes in Germany by Valentina Härter, Birte Sänger, Josephine C. Gieseke, Tanja Gerasimov, Beatrice Hoffmann, Carolin Huisinga, Anja Karow, Lucas J. Müntnich, Natalie E. Palmaers, Stefanie Paquet, Judith Penkert, Diane M. Renz, Tim Ripperger, Farina J. Silchmüller, Christina M. Dutzmann, Christian P. Kratz
Published 2025-09-01Get full text
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Disease characteristics and outcomes of acute myeloid leukemia in germline RUNX1 deficiency (Familial Platelet Disorder with associated Myeloid Malignancy) by Martijn P. T. Ernst, Jurjen Versluis, Peter J. M. Valk, Marc Bierings, Rienk Y. J. Tamminga, Louise H. Hooimeijer, Konstanze Döhner, Paolo Gresele, Kiran Tawana, Saskia M. C. Langemeijer, Bert A. Van der Reijden, Helena Podgornik, Matjaz Sever, Tor H. A. Tvedt, Tom Vulliamy, Jude Fitzgibbon, Inderjeet Dokal, Panagiotis Baliakas, José M. Bastida, Christian Pohlkamp, Torsten Haferlach, Lise Larcher, Jean Soulier, Roger E. G. Schutgens, Kathleen Freson, Nicolas Duployez, Bob Löwenberg, Katrin Ericson, Jörg Cammenga, Tim Ripperger, Marc H. G. P. Raaijmakers
Published 2025-01-01Get full text
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