HOW TO DESIGN THE NEXT CLINICAL TRIAL IN JMML by CHARLOTTE NIEMEYER

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Aplastic anemia in adult and pediatric hematology by Charlotte Niemeyer, (Coordinating Author)

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Pearson syndrome: a multisystem mitochondrial disease with bone marrow failure by Ayami Yoshimi, Kaori Ishikawa, Charlotte Niemeyer, Sarah C. Grünert

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Leukoreductive response to the combination of sorafenib and chemotherapy in hyperleukocytosis of FLT3-ITD mutated pediatric AML by Franziska Schmidt, Miriam Erlacher, Charlotte Niemeyer, Dirk Reinhardt, Jan-Henning Klusmann

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P1000: JUVENILE MYELOMONOCYTIC LEUKEMIA (JMML) INHIBITS T CELL PROLIFERATION VIA THE ECTONUCLEOTIDASE CD39 AND THE PURINERGIC NETWORK by Jovana Rajak, Naile Koleci, Andreea Mesesan, Christian Flotho, Charlotte Niemeyer, Bertram Bengsch, Miriam Erlacher

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THE INTERFACE OF EPIGENETICS AND ENERGY METABOLISM IN JUVENILE MYELOMONOCYTIC LEUKEMIA by Zoé Wehbe, Ruba Hammad, Toni Cathomen, Sheila Bohler, Jovana Rajak, Miriam Erlacher, Foued Ghanjati, Charlotte Niemeyer, Christian Flotho

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ASSOCIATION AND INTERACTIONS OF THE RIO KINASES IN THE CONTEXT OF DIAMOND-BLACKFAN ANEMIA by Hans-Dajo Von Wulffen, Sheila Bohler, Corinna Spohr, Tilman Brummer, Pierre-Emmanuel Gleizes, Alexander Puzik, Charlotte Niemeyer, Miriam Erlacher

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Case Report: Hepatic Adenoma in a Child With a Congenital Extrahepatic Portosystemic Shunt by Hannah Glonnegger, Maren Schulze, Simone Kathemann, Sebastian Berg, Hannah Füllgraf, Andrea Tannapfel, Patrick Gerner, Jochen Grohmann, Charlotte Niemeyer, Simone Hettmer

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ILLUSTRATION OF CLONAL ARCHITECTURE IN JUVENILE MYELOMONOCYTIC LEUKEMIA BY TARGETED SINGLE-CELL DNA SEQUENCING by Foued Ghanjati, Miriam Erlacher, Dirk Lebrecht, Peter Nöllke, Franco Locatelli, European Working Group Of Myelodysplastic Syndromes In Childhood, Charlotte Niemeyer, Christian Flotho

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JUVENILE MYELOMONOCYTIC LEUKEMIA (JMML) CELLS ESCAPE IMMUNE SURVEILLANCE BY MULTIPLE MECHANISMS by Jun Wang, Jovana Rajak, Naile Koleci, Hui Xiao, Anton Niels Wehner, Bertram Bengsch, Juncal Fernandez-Orth, Charlotte Niemeyer, Sheila Bohler, Miriam Erlacher

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A CASE OF KRAS-MUTATED JMML WITH HIGH METHYLATION PROFILE AND PERPLEXED CLINICAL COURSE. by Vasiliki Tzotzola, Kondylia Antoniadi, Charikleia Kelaidi, Loizos Petrikkos, Elda Ioannidou, Evgenios Goussetis, Aikaterini Bountali, Kalliopi Manola, Elpidoforos Mantadakis, Kalliopi Stefanaki, Ioulia Peristeri, Charlotte Niemeyer, Sophia Polychronopoulou

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Clinical and Molecular Heterogeneity of RTEL1 Deficiency by Marcin W. Wlodarski, Marcin W. Wlodarski, Marcin W. Wlodarski, Carsten Speckmann, Carsten Speckmann, Sushree Sangita Sahoo, Sushree Sangita Sahoo, Marta Rizzi, Marta Rizzi, Shinsuke Hirabayashi, Axel Karow, Nina Kathrin Serwas, Nina Kathrin Serwas, Marc Hoemberg, Natalja Damatova, Detlev Schindler, Jean-Baptiste Vannier, Simon J. Boulton, Ulrich Pannicke, Gudrun Göhring, Kathrin Thomay, J. J. Verdu-Amoros, Holger Hauch, Wilhelm Woessmann, Gabriele Escherich, Eckart Laack, Liliana Rindle, Maximilian Seidl, Maximilian Seidl, Anne Rensing-Ehl, Ekkehart Lausch, Christine Jandrasits, Brigitte Strahm, Klaus Schwarz, Stephan R. Ehl, Stephan R. Ehl, Charlotte Niemeyer, Charlotte Niemeyer, Charlotte Niemeyer, Kaan Boztug, Kaan Boztug, Kaan Boztug, Kaan Boztug

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Corrigendum: Clinical and Molecular Heterogeneity of RTEL1 Deficiency by Carsten Speckmann, Carsten Speckmann, Sushree Sangita Sahoo, Sushree Sangita Sahoo, Sushree Sangita Sahoo, Marta Rizzi, Marta Rizzi, Shinsuke Hirabayashi, Axel Karow, Nina Kathrin Serwas, Nina Kathrin Serwas, Marc Hoemberg, Natalja Damatova, Detlev Schindler, Jean-Baptiste Vannier, Simon J. Boulton, Ulrich Pannicke, Gudrun Göhring, Kathrin Thomay, J. J. Verdu-Amoros, Holger Hauch, Wilhelm Woessmann, Gabriele Escherich, Eckart Laack, Liliana Rindle, Maximilian Seidl, Maximilian Seidl, Anne Rensing-Ehl, Ekkehart Lausch, Christine Jandrasits, Brigitte Strahm, Klaus Schwarz, Stephan R. Ehl, Stephan R. Ehl, Charlotte Niemeyer, Charlotte Niemeyer, Charlotte Niemeyer, Kaan Boztug, Kaan Boztug, Kaan Boztug, Kaan Boztug, Marcin W. Wlodarski, Marcin W. Wlodarski, Marcin W. Wlodarski

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IDENTIFICATION OF HIGH-RISK JMML BY BMP4 BISULFITE NEXT-GENERATION SEQUENCING by Foued Ghanjati, Annika Heck, Dirk Lebrecht, Peter Nöllke, Zoé Wehbe, Felicia Andresen, Natalia Rotari, Maximilian Schönung, Daniel Lipka, Miriam Erlacher, European Working Group Of Myelodysplastic Syndromes In Childhood, Charlotte Niemeyer, Christian Flotho

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Abnormal B-Cell Maturation and Increased Transitional B Cells in CBL Syndrome by Francesco Saettini, Tiziana Angela Coliva, Francesca Vendemini, Marta Galbiati, Cristina Bugarin, Riccardo Masetti, Daniele Moratto, Marco Chiarini, Fabiola Guerra, Fabiola Guerra, Maria Iascone, Raffaele Badolato, Giovanni Cazzaniga, Charlotte Niemeyer, Christian Flotho, Andrea Biondi

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Immune dysregulation associated with co-occurring germline CBL and SH2B3 variants by Francesco Baccelli, Davide Leardini, Edoardo Muratore, Daria Messelodi, Salvatore Nicola Bertuccio, Maria Chiriaco, Caterina Cancrini, Francesca Conti, Fausto Castagnetti, Lucia Pedace, Andrea Pession, Ayami Yoshimi, Charlotte Niemeyer, Marco Tartaglia, Franco Locatelli, Riccardo Masetti

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GENOTYPE/PHENOTYPE ASSOCIATIONS IN 174 INDIVIDUALS WITH GERMLINE GATA2 MUTATIONS by Lili Kotmayer, Emilia Kozyra, Maximilian Kaiser, Michael Dworzak, Barbara De Moerloose, Jan Starý, Henrik Hasle, Kirsi Jahnukainen, Sophia Polychronopoulou, Krisztián Kállay, Owen Smith, Shlomit Barzilai, Riccardo Masetti, Jochen Buechner, Marek Ussowicz, Paula Kjollerstrom, Ivana Boďová, Marko Kavcic, Albert Catala, Dominik Turkiewicz, Markus Schmugge, Valérie De Haas, Rebecca Voss, Anna Bigas, Damia Romero, Csaba Bödör, Miriam Erlacher, Alessandra Giorgetti, Charlotte Niemeyer, Marcin Wlodarski

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NPM1 MUTATIONS IN CHILDREN WITH MYELODYSPLASTIC SYNDROME WITH EXCESS BLASTS by Ayami Yoshimi, Miriam Erlacher, Peter Noellke, Senthilkumar Ramamoorthy, Gudrun Göhring, Shlomit Barzilai – Birenboim, Ivana Bodova, Jochen Buechner, Albert Catala, Valérie De Haas, Barbara De Moerloose, Michael Dworzak, Henrik Hasle, Kirsi Jahnukainen, Krisztian Kallay, Marko Kavcic, Paula Kjollerstrom, Franco Locatelli, Riccardo Masetti, Sophia Polychronopoulou, Markus Schmugge, Owen Smith, Jan Stary, Dominik Turkiewicz, Marek Ussowicz, Natalia Rotari, Marcin Wlodarski, Brigitte Strahm, Charlotte Niemeyer

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ONCO-FETAL REPROGRAMMING DRIVES HIGH-RISK JUVENILE MYELOMONOCYTIC LEUKEMIA, WHICH CAN BE TARGETED BY ANTI-CD52 TREATMENT by Mark Hartmann, Maximilian Schönung, Jovana Rajak, Joschka Hey, Valentin Maurer, Ling Hai, Sina Staeble, Jens Langstein, Katharina Bauer, Mariam Hakobyan, Laura Jardine, Sheila Bohler, Dominik Vonficht, Abdul-Habib Maag, Dirk Lebrecht, Katrin M. Bernt, Roland Roelz, Tobias Boch, Eleonora Khabirova, Pavlo Lutsik, Simon Haas, Muzlifah Haniffa, Sam Behjati, Jan-Philipp Mallm, Christian Buske, Michael D. Milsom, Stefan Fröhling, Marc-Jan Bonder, Charlotte Niemeyer, Christian Flotho, Christoph Plass, Miriam Erlacher, Matthias Schlesner, Daniel B. Lipka

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S206: ONCO-FETAL REPROGRAMMING DRIVES HIGH-RISK JUVENILE MYELOMONOCYTIC LEUKEMIA, WHICH CAN BE TARGETED BY ANTI-CD52 TREATMENT by Mark Hartmann, Maximilian Schönung, Jovana Rajak, Joschka Hey, Valentin Maurer, Ling Hai, Sina Staeble, Jens Langstein, Katharina Bauer, Mariam Hakobyan, Laura Jardine, Sheila Bohler, Dominik Vonficht, Abdul-Habib Maag, Dirk Lebrecht, Kathrin Bernt, Roland Rölz, Tobias Boch, Eleonora Khabirova, Pavlo Lutsik, Simon Haas, Muzlifah Haniffa, Sam Behjati, Jan-Philipp Mallm, Christian Buske, Michael Milsom, Stefan Fröhling, Marc-Jan Bonder, Christoph Plass, Charlotte Niemeyer, Christian Flotho, Miriam Erlacher, Matthias Schlesner, Daniel B. Lipka

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