E-mail: hasle@dadlnet.dk
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
- Bone Marrow Immunophenotyping By Flow Cytometry in Refractory Cytopenia of Childhood
- BRAF Mutations in Juvenile Myelomonocytic Leukemia.
- Clinical Impact of Additional Cytogenetic Aberrations and Complex Karyotype In Pediatric 11q23/MLL-Rearranged AML: Results from an International Retrospective Study
- Clonal Mutational Landscape of Childhood Myelodysplastic Syndromes
- Germline Mutations in CBL Cause a Predisposition to Juvenile Myelomonocytic Leukemia
- High Frequency of GATA1 Mutations in Childhood Non-Down Syndrome Acute Megakaryoblastic Leukemia
- 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)
- 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
- 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
- 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
