E-mail: rob.pieters@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
- BCOR and BCORL1 Mutations In Pediatric Acute Myeloid Leukemia
- Bone Marrow Immunophenotyping By Flow Cytometry in Refractory Cytopenia of Childhood
- Comparison of MRD Monitoring By IG/TR Rearrangement and BCR/ABL1 Transcript in Ph+ Pediatric Acute Lymphoblastic Leukemia Patients Treated with Imatinib in the Esphall Study
- DNA Methylation Profiling of Pediatric AML Reveals That Hypomethylation of MN1 Is Characteristic of Inv(16) AML and a Driver of MN1 Overexpression
- Efficacy and Safety of Imatinib on Top of BFM-Like Chemotherapy in Pediatric Patients with Ph+/BCR-ABL+ Acute Lymphoblastic Leukemia (Ph+ALL). the EsPhALL Study
- ETV6 Aberrations Are a Recurrent Event in Pediatric Acute Myeloid Leukemia with Poor Clinical Outcome
- EVI1 Overexpression in Pediatric Acute Myeloid Leukemia Associated with Unfavorable Subtypes
- High IGSF4 expression In Pediatric Acute Monoblastic Leukemia with t(9;11)
- IER3 Expression in Childhood Myelodysplastic Syndrome
- IKZF1 DELETION STATUS DISCRIMINATES FOR OUTCOME IN IMATINIB-TREATED BCR-ABL1-POSITIVE CHILDHOOD ALL
- IKZF1 deletions in Pediatric Acute Myeloid Leukemia
- 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
- Molecular Aberrations in 107 Children with Myelodysplastic Syndrome (MDS)
- 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
- Prognostic Value of Rare IKZF1 deletions in Childhood B-Cell Precursor Acute Lymphoblastic Leukemia: An International Collaborative Study
- Role of MRD in Ph+ Pediatric Acute Lymphoblastic Leukemia Patients Treated with and without Tirosine Kinase Inhibitor in the Esphall Study
- 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 ROLE OF CBL IN RELATION TO RAS-PATHWAY ACTIVATION IN PEDIATRIC AML
- Wilms’ Tumor 1 Gene Mutations in Childhood Acute Myeloid Leukemia: A New Prognostic factor with Implications for MRD Detection
