E-mail: barbara.demoerloose@ugent.be
Odborné práce publikované na Linkos.cz
Přehled odborných textů publikovaných autorem na portálu Linkos.cz. Jsou zde uvedeny knihy a brožury, články v Klinické onkologii, tuzemská abstrakta z databáze abstrakt a další texty. Rejstřík není v žádném případě úplným autorským rejstříkem, protože jsou zde uvedeny pouze texty zveřejněné na portálu Linkos.cz.
Publikovaná abstrakta
- Aberrant DNA Methylation Characterizes a Subtype of Juvenile Myelomonocytic Leukemia (JMML) with Poor Outcome
- APPLICABILITY OF A REPRODUCIBLE FLOW CYTOMETRY SCORING SYSTEM IN THE DIAGNOSIS OF REFRACTORY CYTOPENIA OF CHILDHOOD
- Bone Marrow Immunophenotyping By Flow Cytometry in Refractory Cytopenia of Childhood
- Clinical Impact of Additional Cytogenetic Aberrations and Treatment in Pediatric t(8;21)-Positive AML: Results from an International Retrospective I-BFM-SG Study
- Clinical Impact of Additional Cytogenetic Aberrations, cKIT- and RAS Mutations and Other Factors in Pediatric t(8;21)-AML
- Clonal Mutational Landscape of Childhood Myelodysplastic Syndromes
- COMPARABLE OUTCOME OF IMMUNOSUPPRESSIVE THERAPY WITH RABBIT ANTI-THYMOCYTE GLOBULIN (ATG) PLUS CYCLOSPORINE A (CSA) TO ONE WITH HORSE ATG PLUS CSA IN REFRACTORY CYTOPENIA IN CHILDHOOD
- IER3 Expression in Childhood Myelodysplastic Syndrome
- IMPACT OF MRD STATUS PRIOR TO HSCT IN PEDIATRIC AML
- JMML Revisited: Role Und Outcome of Hematopoietic Stem Cell Transplantation in Subtypes of Juvenile Myelomonocytic Leukemia (JMML)
- LIN28B DEFINES AN AGGRESSIVE SUBTYPE OF JUVENILE MYELOMONOCYTIC LEUKAEMIA
- Molecular Aberrations in 107 Children with Myelodysplastic Syndrome (MDS)
- Mutations of the Spliceosome Complex Genes Occur In Adult Patients but Are Very Rare In Children with Myeloid Neoplasia
- Pediatric Acute Myeloid Leukemia with t(8;16)(p11;p13): A Distinct Clinical and Biological Entity. Results of a Collaborative Study by the International Berlin-Frankfurt-Münster AML Study Group
- Refractory Cytopenia In Childhood (RCC) with Normal Karyotype Is Unlikely to Progress to Advanced MDS Under a Watch and Wait Strategy
- Somatic Genetic and Epigenetic Architecture of Myelodysplastic Syndromes Arising from GATA2 Deficiency
- Switch to Subsequent Line of Treatment in Children and Adolescents with Chronic Myeloid Leukemia (CML) Treated with Imatinib: Experience of the International Registry for Chronic Myeloid Leukemia in Children and Adolescents (I-CML-Ped Study)
- THE CLINICAL RELEVANCE OF MINOR PAROXYSMAL NOCTURNAL HEMOGLOBINURIA CLONES IN REFRACTORY CYTOPENIA OF CHILDHOOD – A PROSPECTIVE STUDY BY EWOG-MDS
- The Integrated Immunological Signature of Refractory Cytopenia of Childhood (RCC)
- Therapy-Related Myelodysplastic Syndrome Following Treatment for Childhood Acute Lymphoblastic Leukemia: Outcome of Patients Registered in the EWOG-MDS 98/06 Studies
- Unexpected High Frequency of GATA2 Mutations in Children with Non-Familial MDS and Monosomy 7
