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                             80 results found
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1 A CASE OF KRAS-MUTATED JMML WITH HIGH METHYLATION PROFILE AND PERPLEXED CLINICAL COURSE. Tzotzola, Vasiliki
2 S1 p.
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2 ACCELERATED CLEARANCE OF ANTI-THYMOCYTE GLOBULIN IN CHILDREN TRANSPLANTED FOR REFRACTORY CYTOPENIA OF CHILDHOOD VERSUS APLASTIC ANEMIA IS ASSOCIATED WITH INCREASED RISK OF GVHD Koopman-Coenen, Eva
2 S1 p.
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3 A COUNTRYWIDE STUDY OF GATA2 DEFICIENCY IN ITALY REVEALS NOVEL SYMPTOMS AND GENOTYPE-PHENOTYPE CORRELATION Roncareggi, Samuele
2 S1 p.
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4 ALLOGENEIC STEM CELL TRANSPLANTATION FOR MYELODYSPLASTIC SYNDROME COMPLICATED BY SYNCHRONOUS ACUTE GRAFT-VS-HOST DISEASE AND CYTOMEGALOVIRUS INFECTION Fraga, Ana
2 S1 p.
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5 ASSOCIATION AND INTERACTIONS OF THE RIO KINASES IN THE CONTEXT OF DIAMOND-BLACKFAN ANEMIA Wulffen, Hans-Dajo Von
2 S1 p.
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6 BCR:ABL-NEGATIVE MYELOPROLIFERATIVE NEOPLASMS IN CHILDREN AND ADOLESCENTS: INCREASED DISEASE BURDEN IN PATIENTS WITH JAK2 MUTATION, UNMET DIAGNOSTIC NEEDS AND OPTIMAL TREATMENT OPTIONS Kelaidi, Charikleia
2 S1 p.
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7 BIOLOGY OF BONE MARROW DISORDER CHARACTERIZE DISTINCT SUBTYPES OF REFRACTORY CYTOPENIA OF CHILDHOOD (RCC) Sukova, Martina
2 S1 p.
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8 CAN A THIRD HAEMATOPOIETIC STEM CELL TRANSPLANTATION BE A VIABLE OPTION FOR JMML RELAPSE? A CASE REPORT Vendemini, Francesca
2 S1 p.
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9 CASE REPORT: AN UNUSUAL CASE OF REFRACTORY CYTOPENIA OF CHILDHOOD IN A PATIENT WITH DOWN SYNDROME? Viana, Viviany
2 S1 p.
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10 CHEK2 GERMLINE VARIANTS AND ALLOGENEIC HEMATOPOIETIC STEM CELL TRANSPLANT OUTCOMES Lahtinen, Atte K
2 S1 p.
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11 CHILDHOOD MYELODYSPLASTIC NEOPLASM: GENETIC VARIANTS AND THEIR IMPACT ON DIAGNOSIS AND PROGNOSIS Lovatel, Viviane
2 S1 p.
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12 CLINICAL AND HEMATOLOGICAL PROFILE OF CHILDREN WITH CYTOPENIAS REFERRED TO THE BRAZILIAN COOPERATIVE GROUP OF PEDIATRIC MYELODYSPLASTIC SYNDROME Rosa, Caroline Ramalho
2 S1 p.
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13 "CLONAL ARCHITECTURE IN JUVENILE MYELOMONOCYTIC LEUKEMIA" Flotho, Christian
2 S1 p.
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14 CLONAL HEMATOPOIESIS IN SHWACHMAN DIAMOND SYNDROME: BIOLOGY AND CLINICAL IMPLICATIONS Shimamura, Akiko
2 S1 p.
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15 DEVELOPMENT OF NEW GENE EDITING APPROACHES FOR BONE MARROW FAILURE AND MDS PREDISPOSITION SYNDROMES Krzyzanowski, Damian
2 S1 p.
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16 DIAGNOSIS OF JUVENILE MYELOMONOCYTIC LEUKEMIA, IN CHILDREN WITH NEUROFIBROMATOSIS TYPE 1 – CASE REPORT Silva, Rita Aldeia Da
2 S1 p.
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17 DYSLIPIDEMIA AFTER INTENSIVE IMMUNOSUPPRESSIVE THERAPY VERSUS HEMATOPOIETIC STEM CELL TRANSPLANTATION IN APLASTIC ANEMIA: A SINGLE-CENTER EXPERIENCE Holeczek, C
2 S1 p.
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18 EARLY RELAPSE DETECTION IN JMML PATIENTS FOLLOWING HAEMATOPOIETIC STEM CELL TRANSPLANT Kricke, Susanne
2 S1 p.
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19 EPIDEMIOLOGICAL ANALYSIS OF CONSTITUTIONAL AND ACQUIRED APLASTIC ANEMIA IN LATVIA: 1998-2022 Racko, Iveta
2 S1 p.
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20 FUNCTIONAL ANALYSES OF RUNX1 VARIANTS IN THE CONTEXT OF FAMILIAL PLATELET DISORDER WIT PREDISPOSITION TO HEMATOLOGIC MALIGNANCIES Decker, Melanie
2 S1 p.
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21 GATA2 DEFICIENCY SYNDROME: MDS / ACUTE MYELOID LEUKEMIA IN AN ADOLESCENT PATIENT Yilmaz, Sebnem
2 S1 p.
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22 GENOME SEQUENCING APPROACHES FOR DIAGNOSIS AND DISCOVERY OF BMF/MDS SPECIFIC GENETIC ALTERATIONS Wlodarski, Marcin
2 S1 p.
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23 GENOMIC LANDSCAPE AND SINGLE BASE SUBSTITUTION MUTATIONAL SIGNATURES IN JUVENILE MYELOMONOCYTIC LEUKEMIA: A NEW JMML PORTRAIT Peloso, Alberto
2 S1 p.
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24 GENOTYPE/PHENOTYPE ASSOCIATIONS IN 174 INDIVIDUALS WITH GERMLINE GATA2 MUTATIONS Kotmayer, Lili
2 S1 p.
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25 GERMLINE LOSS-OF-FUNCTION MUTATIONS IN MDM4 CAUSE A NEW BONE MARROW FAILURE SYNDROME WITH TP53- DEPENDENT HEMATOPOIETIC CELL DEATH Sharma, Richa
2 S1 p.
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26 HEPATITIS-ASSOCIATED MYELODYSPLASTIC SYNDROME IN CHILDREN: REPORT OF 2 CASES Pegoraro, Francesco
2 S1 p.
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27 HOMOZYGOUS CBL MUTATION IN B LYMPHOCYTES AFTER CBL-DRIVEN JMML IMPAIRS B CELL MATURATION, FUNCTION AND ANTIBACTERIAL IMMUNITY Bohlen, Jonathan
2 S1 p.
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28 HOSPITAL ADMISSIONS OF APLASTIC ANAEMIA: REAL WORLD EVIDENCE FROM UK CHILDREN ADMITTED FROM 2017 – 2022 Famokunwa, Bamidele
2 S1 p.
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29 HOW TO DESIGN THE NEXT CLINICAL TRIAL IN JMML NIEMEYER, CHARLOTTE
2 S1 p.
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30 HSCORE CALCULATION AT DIAGNOSIS AND DURING PATIENT FOLLOW-UP IN TWO CHILDREN WITH MALIGNANCY-ASSOCIATED HEMOPHAGOCYTIC SYNDROME Kaya, Zühre
2 S1 p.
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31 IDENTIFICATION OF FUNCTIONAL DEFECTS LEADING TO BONE MARROW FAILURE IN GATA2 DEFICIENCY Wantzen, Charlotte
2 S1 p.
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32 IDENTIFICATION OF HIGH-RISK JMML BY BMP4 BISULFITE NEXT-GENERATION SEQUENCING Ghanjati, Foued
2 S1 p.
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33 ILLUSTRATION OF CLONAL ARCHITECTURE IN JUVENILE MYELOMONOCYTIC LEUKEMIA BY TARGETED SINGLE-CELL DNA SEQUENCING Ghanjati, Foued
2 S1 p.
 article
34 IMMUNOPHENOTYPE IN SAMD9/9L SYNDROME: CORRELATIONS WITH MORPHOLOGY Kelaidi, Charikleia
2 S1 p.
 article
35 IMMUNOSUPPRESSIVE THERAPY IN A PATIENT WITH SAA-like RCC AND GATA2 DEFICIENCY Kroiss, D
2 S1 p.
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36 IMPACT PROGNOSIS OF CYTOGENETIC ALTERATIONS IN BRAZILIAN CHILDHOOD MYELODYSPLASTIC NEOPLASM Lovatel, Viviane
2 S1 p.
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37 IMPLICATIONS OF NOVEL CLASSIFICATIONS OF MYELOID NEOPLASMS FOR CHILDHOOD MDS Calvo, Katherine R.
2 S1 p.
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38 INFANT EXTRAMEDULLARY KMT2A REARRANGED T/MYELOID ACUTE LEUKEMIA MIMICKING LANGERHANS CELL HISTIOCYTOSIS Vakrmanova, Barbora
2 S1 p.
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39 INFANT WITH SAMDL9 MUTATION, MONOSOMY 7 AND ACUTE LYMPHOBLASTIC LEUKEMIA Pavlovic, Maja
2 S1 p.
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40 INTENSIVE CHEMOTHERAPY AS BRIDGING TO STEM CELL TRANSPLANTATION IN 5 YEAR OLD GIRL WITH JUVENILE MYELOMONOCYTIC LEUKEMIA– CASE REPORT Chyżyński, Bartosz
2 S1 p.
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41 INVESTIGATING AND MODULATING LEUKEMIA INITIATING CELLS TO REDUCE RISK OF POST-TRANSPLANT RELAPSE IN JMML Xiao, Hui
2 S1 p.
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42 JMML WITH NRAS MUTATION IN ELANE ASSOCIATED SEVERE CONGENITAL NEUTROPENIA Uhlving, Hilde Hylland
2 S1 p.
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43 JUVENILE MYELOMONOCYTIC LEUKEMIA (JMML) CELLS ESCAPE IMMUNE SURVEILLANCE BY MULTIPLE MECHANISMS Wang, Jun
2 S1 p.
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44 JUVENILE MYELOMONOCYTIC LEUKEMIA WITH TELOMERE SHORTENING: CASE REPORT Oliveira, Anita Frisanco
2 S1 p.
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45 LOSS OF HSC STEMNESS IDENTITY IS ASSOCIATED WITH EXHAUSTION AND HYPORESPONSIVENESS IN GATA2 DEFICIENCY SYNDROME Largeaud, Laëtitia
2 S1 p.
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46 MYELODYSPLASIA-RELATED CYTOGENETIC ABNORMALITES IN CHILDHOOD ACUTE MYELOID LEUKEMIA – A 20-YEAR I-BFM- AML COLLABORATIVE DATABASE STUDY Sandahl, Kristian Juul
2 S1 p.
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47 MYELODYSPLASTIC SYNDROME AND LEUKEMIA IS A SECONDARY EVENT AFTER BONE MARROW FAILURE IN GATA2 HAPLOINSUFFICIENT MICE Koyunlar, Cansu
2 S1 p.
 article
48 NATIONAL EXPERIENCE WITH IMMUNOSUPPRESSIVE THERAPY AND ELTROMBOPAG IN CHILDREN WITH APLASTIC ANEMIA- REAL WORLD DATA Pawelec, Katarzyna
2 S1 p.
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49 NATURAL HISTORY OF RALD: A 20 YEAR FOLLOW-UP OF A NRAS MUTATED PATIENT EXCLUDING A MALIGNANT PROGRESSION Attardi, Enrico
2 S1 p.
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50 NEXT GENERATION SEQUENCING APPROACH TO BONE MARROW FAILURE SYNDROMES – PORTUGUESE EXPERIENCE Coucelo, Margarida
2 S1 p.
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51 NOVEL APPROACHES TARGETING THE RAS PATHWAY IN JMML Stieglietz, Elliot
2 S1 p.
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52 NPM1 MUTATIONS IN CHILDREN WITH MYELODYSPLASTIC SYNDROME WITH EXCESS BLASTS Yoshimi, Ayami
2 S1 p.
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53 ONCO-FETAL REPROGRAMMING DRIVES HIGH-RISK JUVENILE MYELOMONOCYTIC LEUKEMIA, WHICH CAN BE TARGETED BY ANTI-CD52 TREATMENT Hartmann, Mark
2 S1 p.
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54 OPTICAL GENOME MAPPING: A NEW TOOL TO OVERCOME CONVENTIONAL CYTOGENETICS’ LIMITATIONS IN PATIENTS WITH BONE MARROW FAILURE. Zubicaray, Josune
2 S1 p.
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55 OUTCOMES OF HEMATOPOIETIC STEM CELL TRANSPLANTATION IN PEDIATRIC PATIENTS WITH MYELODYSPLASTIC SYNDROME AND ACUTE MYELOID LEUKEMIA SECONDARY TO INHERITED BONE MARROW FAILURE SYNDROMES Sanjuán, Laura Murillo
2 S1 p.
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56 PATHWAY-DIRECTED THERAPY APPROACH IN PEDIATRIC MDS AND AML De Moerloose, Barbara
2 S1 p.
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57 PEDIATRIC MDS IN GATA2-DEFICIENCY: ENHANCED HISTONE TRIMETHYLATION AND DEREGULATED APOPTOSIS AS DRIVER? Schreiber, Franziska
2 S1 p.
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58 PERIPHERAL AND BONE MARROW G-CSF-RELATED MYELOBLASTS RATE IN A PATIENT WITH SEVERE CONGENITAL NEUTROPENIA Trambusti, Irene
2 S1 p.
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59 PITFALLS IN THE DIAGNOSTICS OF SAA/RCC: CAN WHOLE EXOME SEQUENCING LEAD US THE WAY? Novak, Wolfgang
2 S1 p.
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60 PREVALENCE OF EXPOSURE TO SOCIO-ENVIRONMENTAL FACTORS IN MYELODYSPLASTIC SYNDROMES - A STUDY OF THE BRAZILIAN PEDIATRIC MYELODYSPLASTIC SYNDROME GROUP (GCB-SMD-PED) Murra, Glaucia Regina Costa
2 S1 p.
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61 PUMA-INDUCED APOPTOSIS DRIVES BONE MARROW FAILURE UPON TELOMERE SHORTENING AND LEUKEMIA IN A MOUSE MODEL OF DYSKERATOSIS CONGENITA Molnar, Christian
2 S1 p.
 article
62 RECURRENCE OF UNDERLYING CONGENITAL NEUTROPENIA WITHOUT MDS AFTER ALLOGENEIC STEM CELL TRANSPLANTATION IN A PATIENT WITH ELANE-MUTATED CONGENITAL NEUTROPENIA AND SECONDARY MDS Furlan, Ingrid
2 S1 p.
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63 REFRACTORY CYTOPENIA OF CHILDHOOD: CLINICAL FEATURES, PATHOLOGIC FINDINGS AND EXPERIENCE OF BRAZILIAN COOPERATIVE GROUP OF PEDIATRIC MYELODYSPLASTIC SYNDROME Rosa, Caroline Ramalho
2 S1 p.
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64 RELAPSED UBTF-TD MDS TREATED WITH VENETOCLAX AND AZACITIDINE Hasle, Henrik
2 S1 p.
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65 RIC VS MAC IN ALLO-HSCT FOR CHILDHOOD MYELODYSPLASTIC SYNDROME Morozova, Elena
2 S1 p.
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66 SH2B3 GERMLINE MUTATION CAUSE A MULTISYSTEM DISORDER WITH PREDISPOSITION TO MYELOPROLIFERATIVE NEOPLASMS Leardini, Davide
2 S1 p.
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67 SPECTRUM OF CLINICAL PHENOTYPES AND SOMATIC VARIANTS IN RUNX1-ASSOCIATED FAMILIAL PLATELET DISORDER WITH PREDISPOSITION TO HEMATOLOGIC MALIGNANCIES Förster, Alisa
2 S1 p.
 article
68 TELOMERE LENGHT AND CYTOPENIAS: ANALYSIS OF CHILDREN REFERRED TO BRAZILIAN COOPERATIVE GROUP OF CHILDHOOD MYELODYSPLASTIC SYNDROME Balceiro, Rafael
2 S1 p.
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69 THE CLINICAL SPECTRUM AND BIOLOGICAL FINDINGS IN RAS-ASSOCIATED JUVENILE MYELOMONOCYTIC LEUKEMIA AND RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER Verhulst, Hanne
2 S1 p.
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70 THE INTERFACE OF EPIGENETICS AND ENERGY METABOLISM IN JUVENILE MYELOMONOCYTIC LEUKEMIA Wehbe, Zoé
2 S1 p.
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71 THE NEW KID ON THE BLOCK: UBTF-TD Erlacher, Miriam
2 S1 p.
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72 THERAPY-RELATED MYELODYSPLASTIC SYNDROMES (t-MDS) IN CHILDHOOD: THE EXPERIENCE OF THE HELLENIC STUDY GROUP FOR MDS/JMML/SAA, MEMBER OF THE EWOG-MDS/SAA WORKING GROUP Petrikkos, Loizos
2 S1 p.
 article
73 The rare cases of co-occurrences of Down Syndrome Disease and Juvenile Myelomonocytic Leukemia Buldini, Barbara
2 S1 p.
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74 THE ROLE OF ALLOGENEIC HEMATOPOIETIC STEM CELL TRANSPLANTATION IN APLASTIC ANEMIA Strahm, Brigitte
2 S1 p.
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75 THIRTY YEARS OF EXPERIENCE IN THE TREATMENT OF CHILDHOOD APLASTIC ANEMIA IN LITHUANIA Rutkauskaite, Vilma
2 S1 p.
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76 UNRAVELING THE MOLECULAR BASIS OF PEDIATRIC MYELODYSPLASTIC SYNDROME: INSIGHTS FROM CRISPR/CAS9-EDITED IPSCS BEARING THE SAMD9 P.I1567M MUTATION Pera, Joan
2 S1 p.
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77 VARIABLE CLINICAL COURSES OF VARICELLA ZOSTER VIRUS INFECTION- OR VACCINATION-RELATED BONE MARROW FAILURE Toskov, Vasil
2 S1 p.
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78 VARIANT PROFILING IN PEDIATRIC CHRONIC MYELOID LEUKEMIA Behrens, Yvonne Lisa
2 S1 p.
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79 VENETOCLAX-BASED THERAPIES IN PEDIATRIC ADVANCED MDS AND RELAPSED/REFRACTORY AML: A MULTICENTER RETROSPECTIVE ANALYSIS Masetti, Riccardo
2 S1 p.
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80 WHAT CAN WE DEDUCE FROM MOLECULAR CLASSIFICATION OF MYELOID NEOPLASIA FOR THERAPY IN PEDIATRICS? Hasle, Henrik
2 S1 p.
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                             80 results found
 
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