E-mail: m.vandenheuvel@erasmusmc.nl
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
- A Complex Karyotype but Not Monosomy 7 Is an Independent Prognostic Factor in Advanced Childhood MDS.
- 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
- BCOR and BCORL1 Mutations In Pediatric Acute Myeloid Leukemia
- Bone Marrow Immunophenotyping By Flow Cytometry in Refractory Cytopenia of Childhood
- BRAF Mutations in Juvenile Myelomonocytic Leukemia.
- 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
- Differences in Cyto- and Molecular Genetic Abnormalities between Children
- DNA Methylation Profiling of Pediatric AML Reveals That Hypomethylation of MN1 Is Characteristic of Inv(16) AML and a Driver of MN1 Overexpression
- ETV6 Aberrations Are a Recurrent Event in Pediatric Acute Myeloid Leukemia with Poor Clinical Outcome
- Germline Mutations in CBL Cause a Predisposition to Juvenile Myelomonocytic Leukemia
- HIGH GATA2 EXPRESSION IS A POOR PROGNOSTIC MARKER IN PEDIATRIC ACUTE MYELOID LEUKEMIA
- HLA-Identical Umbilical Cord Blood Transplantation from a Sibling Donor in Juvenile myelomonocytic Leukemia
- Characterization of CEBPA Mutations and Promoter Hypermethylation in Pediatric Acute Myeloid Leukemia
- Identification of Gene Expression Signatures Accurately Predicting Cytogenetic Subtypes in Pediatric Acute Myeloid Leukemia
- IER3 Expression in Childhood Myelodysplastic Syndrome
- IKZF1 deletions in Pediatric Acute Myeloid Leukemia
- Is Prevention of Myeloid Leukemia Possible?
- 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
- Microrna Expression Profiling In Pediatric Acute Myeloid Leukemia Reveals a Tumor-Suppressive Role Of Mir-9 Associated With Translocation (8;21)
- Microrna-106b~25 Cluster Is Involved in Relapsed MLL-Rearranged Pediatric AML
- MicroRNA-196a and –196b Are Differentially Expressed Between and within Cytogenetic and Molecular Subtypes of Pediatric Acute Myeloid Leukemia, and High Expression Is Correlated to Overexpression of HOX Genes
- 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
- Myeloid Leukemia of Down Syndrome: The Results of An International Retrospective Study
- NUP98/JARID1A Is a New Recurrent Genetic Abnormality in Pediatric Acute Megakaryoblastic Leukemia with a Distinct HOX-Gene Expression Pattern
- Overexpression of BRE in Pediatric MLL-Rearranged Acute Myeloid Leukemia Associated with t(9;11)(p22;q23)
- 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
- Prognostic Relevance of Recurrent Genetic Aberrations in Pediatric Acute Megakaryoblastic Leukemia
- 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
- T-Cell Receptor V CDR3 Oligoclonality Frequently Occurs in Childhood Refractory Cytopenia and Severe Aplastic Anemia.
- Telomere Length and Telomerase Complex Mutations in Pediatric Acute Myeloid Leukemia
- THE CLINICAL RELEVANCE OF BAALC AND ERG EXPRESSION LEVELS IN PEDIATRIC AML
- 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)
- The Mir-193 Family Antagonizes Stem Cell Pathways and Is a Potent Tumor Suppressor in Childhood and Adult Acute Myeloid Leukemia
- THE ROLE OF CBL IN RELATION TO RAS-PATHWAY ACTIVATION IN PEDIATRIC AML
- 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
- Wilms’ Tumor 1 Gene Mutations in Childhood Acute Myeloid Leukemia: A New Prognostic factor with Implications for MRD Detection
