Search Results - "WLODARSKI, M"

Recommendations on hematopoietic stem cell transplantation for inherited bone marrow failure syndromes by 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

“…Allogeneic hematopoietic stem cell transplantation (HSCT) offers the potential to cure patients with an inherited bone marrow failure syndrome (IBMFS)…”
Get full text

Mutational landscape in children with myelodysplastic syndromes is distinct from adults: specific somatic drivers and novel germline variants by 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

Get full text

Germline SAMD9 mutation in siblings with monosomy 7 and myelodysplastic syndrome by 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

Get full text

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

“…Germline SAMD9 and SAMD9L mutations (SAMD9/9Lmut) cause a novel bone marrow failure and pediatric myelodysplastic syndrome. Despite >400 patients reported,…”
Get full text

Cytomegalovirus‐Specific Regulatory and Effector T Cells Share TCR Clonality—Possible Relation to Repetitive CMV Infections by 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.

“…Cytomegalovirus (CMV) infections have a major impact on morbidity and mortality of transplant patients. Among the complex antiviral T‐cell response, CMV‐IE‐1…”
Get full text

Chilblain lupus and steroid‐responsive pancytopenia precede monosomy 7‐linked AML as manifestation of rasopathy by 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.

Get full text

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

Get full text

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

“…N/A…”
Get full text

P816: TRANSIENT MONOSOMY 7 IN SAMD9/9L SYNDROMES: IS IT SAFE TO WATCH AND WAIT? by 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.

Get full text

Integrated Analysis of Epigenetic and Genetic Changes During MDS Progression Reveals the Tight Association of Epigenetic Changes with Genetic Selection by 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

Get full text

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

“…Summary Double‐negative (DN) regulatory T cells (Tregs) are specialized T lymphocytes involved in the down‐modulation of immune responses, resulting in…”
Get full text

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

Get full text

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

Get full text

48 GATA2-RELATED MYELODYSPLASTIC SYNDROMES (MDS): PREVALENCE, CLINICAL CHARACTERISTICS AND PROGNOSIS by 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

Get full text

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

“…In paroxysmal nocturnal hemoglobinuria (PNH), clonal expansion of glycosylphosphatidylinositol-anchored proteins (GPI-AP)-deficient cells leads to a syndrome…”
Get full text

P-52 Study of DNA repair geneexpression in MDS patients with shortened telomeres and multiple chromosomal abnormalities by array-based comparative genomic hybridization (A-CGH) by Gondek, L., O'Keefe, C., Wlodarski, M., Maciejewski, J.P.

Get full text

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

Get full text

Topic: AS04-MDS Biology and Pathogenesis/AS04d-Somatic mutations: THE EVOLVING GENETIC LANDSCAPE OF PEDIATRIC MDS-EB by 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.

Get full text

Loss of B cells and their precursors is the most constant feature of GATA-2 deficiency in childhood myelodysplastic syndrome by 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

“…GATA-2 deficiency was recently described as common cause of overlapping syndromes of immunodeficiency, lymphedema, familiar myelodysplastic syndrome or acute…”
Get full text

190 - New Development in Childhood MDS by Niemeyer, C., Strahm, B., Pastor, V., Flotho, C., Yoshimi, A., Wlodarski, M.

Get full text