Recommendations on hematopoietic stem cell transplantation for inherited bone marrow failure syndromes von Peffault de Latour, R, Peters, C, Gibson, B, Strahm, B, Lankester, A, de Heredia, C D, Longoni, D, Fioredda, F, Locatelli, F, Yaniv, I, Wachowiak, J, Donadieu, J, Lawitschka, A, Bierings, M, Wlodarski, M, Corbacioglu, S, Bonanomi, S, Samarasinghe, S, Leblanc, T, Dufour, C, Dalle, J-H

Volltext

Germline SAMD9 mutation in siblings with monosomy 7 and myelodysplastic syndrome von Schwartz, J R, Wang, S, Ma, J, Lamprecht, T, Walsh, M, Song, G, Raimondi, S C, Wu, G, Walsh, M F, McGee, R B, Kesserwan, C, Nichols, K E, Cauff, B E, Ribeiro, R C, Wlodarski, M, Klco, J M

Volltext

Mutational landscape in children with myelodysplastic syndromes is distinct from adults: specific somatic drivers and novel germline variants von Pastor, V, Hirabayashi, S, Karow, A, Wehrle, J, Kozyra, E J, Nienhold, R, Ruzaike, G, Lebrecht, D, Yoshimi, A, Niewisch, M, Ripperger, T, Göhring, G, Baumann, I, Schwarz, S, Strahm, B, Flotho, C, Skoda, R C, Niemeyer, C M, Wlodarski, M W

Volltext

SIGNATURES OF SOMATIC GENETIC RESCUE IN SAMD9/9L SYNDROMES: DIAGNOSTIC AND PROGNOSTIC UTILITY von Gray, N., Boals, M., Lewis, S., Yoshida, M., Sahoo, S., Wlodarski, M.

Volltext

Cytomegalovirus‐Specific Regulatory and Effector T Cells Share TCR Clonality—Possible Relation to Repetitive CMV Infections von Schwele, S., Fischer, A. M., Brestrich, G., Wlodarski, M. W., Wagner, L., Schmueck, M., Roemhild, A., Thomas, S., Hammer, M. H., Babel, N., Kurtz, A., Maciejewski, J. P., Reinke, P., Volk, H.‐D.

Volltext

Chilblain lupus and steroid‐responsive pancytopenia precede monosomy 7‐linked AML as manifestation of rasopathy von Klobassa, D.S., Dworzak, M.N., Lanz, S., Skrabl‐Baumgartner, A., Beham‐Schmid, C., Cerroni, L., Haas, O.A., Wlodarski, M., Salzer, U., Lackner, H., Benesch, M., Schwinger, W., Urban, C., Seidel, Markus G.

Volltext

New Development in Childhood MDS von Niemeyer, C, Strahm, B, Pastor, V, Flotho, C, Yoshimi, A, Wlodarski, M

Volltext

P816: TRANSIENT MONOSOMY 7 IN SAMD9/9L SYNDROMES: IS IT SAFE TO WATCH AND WAIT? von Erlacher, M., Andresen, F., Yoshimi, A., Sukova, M., Stary, J., Moerloose, B., Dworzak, M., Polychronopoulou, S., Göhring, G., Kratz, C., Werff ten Bosch, J., Seidel, M., Strahm, B., Wlodarski, M., Niemeyer, C.

Volltext

Twelfth European Students’ Conference von Geisler, B., Akdenizli, K., Neidhardt, A., Ovaska, E., Recklinghausen, J. V., Schuster, A., Wirth, L., Wlodarski, M.

Volltext

Integrated Analysis of Epigenetic and Genetic Changes During MDS Progression Reveals the Tight Association of Epigenetic Changes with Genetic Selection von Pohl, S, Heudobler, D, Loyola, V. Bengt Pastor, Gebhard, C, Mossner, M, Jann, J.C, Hirabayashi, S, Nowak, D, Wlodarski, M, Hofmann, W.K, Niemeyer, C, Rehli, M

Volltext

Double‐negative regulatory T cells induce allotolerance when expanded after allogeneic haematopoietic stem cell transplantation von McIver, Z., Serio, B., Dunbar, A., O’Keefe, C. L., Powers, J., Wlodarski, M., Jin, T., Sobecks, R., Bolwell, B., Maciejewski, J. P.

Volltext

O-026 Genome-wide methylation profiling by MCIp-Seq reveals aberrant DNA methylation patterns in childhood MDS with GATA2-deficiency von Pohl, S, Heudobler, D, Gebhard, C, Hirabayashi, S, Niemeyer, C, Wlodarski, M, Rehli, M

Volltext

48 GATA2-RELATED MYELODYSPLASTIC SYNDROMES (MDS): PREVALENCE, CLINICAL CHARACTERISTICS AND PROGNOSIS von Wlodarski, M, Hirabayashi, S, Pastor, V, Stary, J, Hasle, H, Masetti, R, Dworzak, M, Schmugge, M, van den Heuvel-Eibrink, M, De Moerloose, B, Ussowicz, M, Catala, A, Smith, O, Goehring, G, Schlegelberger, B, Locatelli, F, Makishima, H, Maciejewski, J, Strahm, B, Niemeyer, C

Volltext

P-026 The role of autophagy in the etiology and malignant transformation of myeloid cells with ribosomal protein haploinsufficiencies von MacInnes, A, Heijnen, H, Van Wijk, R, Van den Loosdrecht, A, Bierings, M, Gazda, H, Wlodarski, M

Volltext

Large granular lymphocyte (LGL)-like clonal expansions in paroxysmal nocturnal hemoglobinuria (PNH) patients von RISITANO, A. M, MACIEJEWSKI, J. P, MURANSKI, P, WLODARSKI, M, O'KEEFE, C, SLOAND, E. M, YOUNG, N. S

Volltext

GENETIC ORIGINS AND CLONAL TRAJECTORIES IN PEDIATRIC MYELODYSPLASTIC SYNDROMES von Sahoo, S., Pastor, V., Goodings-Harris, C., (Ewog-Mds), E.W.G.O.C.M., Strahm, B., Noellke, P., Niemeyer, C., Wlodarski, M.

Volltext

Loss of B cells and their precursors is the most constant feature of GATA-2 deficiency in childhood myelodysplastic syndrome von Nováková, Michaela, Žaliová, Markéta, Suková, Martina, Wlodarski, Marcin, Janda, Aleš, Froňková, Eva, Campr, Vít, Lejhancová, Kateřina, Zapletal, Ondřej, Pospíšilová, Dagmar, Černá, Zdeňka, Kuhn, Tomáš, Švec, Peter, Pelková, Vendula, Zemanová, Zuzana, Kerndrup, Gitte, van den Heuvel-Eibrink, Marry, van der Velden, Vincent, Niemeyer, Charlotte, Kalina, Tomáš, Trka, Jan, Starý, Jan, Hrušák, Ondřej, Mejstříková, Ester

Volltext

Topic: AS04-MDS Biology and Pathogenesis/AS04d-Somatic mutations: THE EVOLVING GENETIC LANDSCAPE OF PEDIATRIC MDS-EB von Erlacher, M., Yoshimi, A., Stasik, S., Ramamoorthy, S., Lebrecht, D., Noellke, P., Goehring, G., De Haas, V., Starý, J., Masetti, R., Ussowicz, M., Barzilai-Birenboim, S., De Moerloose, B., Kállay, K., Buechner, J., Dworzak, M., Catala, A., Hasle, H., Schmugge, M., Polychronopoulou, S., Boďová, I., Jahnukainen, K., Smith, O., Kavcic, M., Turkiewicz, D., Kjollerstrom, P., Locatelli, F., Wlodarski, M., Thiede, C., Strahm, B., Niemeyer, C.

Volltext

Topic: AS07-Singular Entities/Subtypes/AS07c-Hereditary MDS including predisposition syndromes von Bortnick, R., Wlodarski, M., De Haas, V., De Moerloose, B., Dworzak, M., Hasle, H., Masetti, R., Stary, J., Turkiewicz, D., Ussowicz, M., Kozyra, E., Albert, M., Bader, P., Bordon, V., Cario, G., Beier, R., Schulte, J., Bresters, D., Mueller, I., Pichler, H., Sedlacek, P., Sauer, M., Zecca, M., Göhring, G., Yoshimi, A., Noellke, P., Erlacher, M., Locatelli, F., Niemeyer, C., Strahm, B.

Volltext

P47 - Topic: AS07-Singular Entities/Subtypes/AS07c-Hereditary MDS including predisposition syndromes: HEMATOPOIETIC STEM CELL TRANSPLANTATION IN CHILDREN AND ADOLESCENTS WITH GATA2... von Bortnick, R., Wlodarski, M., De Haas, V., De Moerloose, B., Dworzak, M., Hasle, H., Masetti, R., Stary, J., Turkiewicz, D., Ussowicz, M., Kozyra, E., Albert, M., Bader, P., Bordon, V., Cario, G., Beier, R., Schulte, J., Bresters, D., Mueller, I., Pichler, H., Sedlacek, P., Sauer, M., Zecca, M., Göhring, G., Yoshimi, A., Noellke, P., Erlacher, M., Locatelli, F., Niemeyer, C., Strahm, B.

Volltext