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