29 results on '"Stary, J."'
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2. P47 - Topic: AS07-Singular Entities/Subtypes/AS07c-Hereditary MDS including predisposition syndromes: HEMATOPOIETIC STEM CELL TRANSPLANTATION IN CHILDREN AND ADOLESCENTS WITH GATA2-RELATED MYELODYSPLASTIC SYNDROME
3. O27 - Topic: AS06-Prognosis/AS06b-Predictive factors of response to treatment: OUTCOMES OF RELAPSED JUVENILE MYELOMONOCYTIC LEUKEMIA: THE ROLE OF SECOND HEMATOPOIETIC STEM CELL TRANSPLANTATION
4. O05 - Topic: AS04-MDS Biology and Pathogenesis/AS04b-Clonal diversity & evolution: SOMATIC GENETIC RESCUE IN SAMD9/SAMD9L MDS PREDISPOSITION SYNDROMES
5. Topic: AS07-Singular Entities/Subtypes/AS07c-Hereditary MDS including predisposition syndromes
6. Topic: AS06-Prognosis/AS06b-Predictive factors of response to treatment
7. Topic: AS04-MDS Biology and Pathogenesis/AS04b-Clonal diversity & evolution
8. 48 GATA2-RELATED MYELODYSPLASTIC SYNDROMES (MDS): PREVALENCE, CLINICAL CHARACTERISTICS AND PROGNOSIS
9. 232 Relevance of WT1 expression, mutations and single nucleotide polymorphisms in juvenile myelomonocytic leukemia
10. 233 IER3 in childhood myelodysplastic syndrome
11. P047 T-cell receptor (TCR) Vbeta CDR3 oligoclonality frequently occurs in childhood refractory cytopenia (MDS-RC)
12. P079 BRAF mutations in juvenile myelomonocytic leukemia
13. C029 Hematopoietic stem cell transplantation for advanced primary MDS in children: results of a retrospective analysis from the EWOG-MDS group
14. C030 Hematopoietic stem cell transplantation after a myeloablative conditioning regimen in children with refractory cytopenia: results of a retrospective analysis from the EWOG-MDS group
15. O-45 Treatment for patients relapsingwith juvenile myelomonocytic leukemia after allogeneic stem cell transplantation: The EWOG-MDS study
16. Loss of heterozygosity and heterogeneity of its appearance and persisting in the course of acute myeloid leukemia and myelodysplastic syndromes
17. Prediction and reversion of post-transplant relapse in patients with chronic myeloid leukemia using mixed chimerism and residual disease detection and adoptive immunotherapy
18. Characteristics and outcome of treatment-related MDS after childhood cancer: The EWOG-MDS experience
19. Case forum: Capillary leak syndrome—An unusual complication of MDS-RAEB?
20. Immunophenotype of bone marrow subsets in Czech patients reported into eWOG-MDS database. Proposal of a standard panel of monoclonal antibodies
21. T-cell receptor (TCR)Vβ repertoire analysis: A valuable diagnostic tool for pediatric MDS and SAA?
22. Case forum: Natural course of MPS/MDS overlap disease (JMML, CMML, RAEB-t) during 14 years of follow-up in a child with NF-1
23. Clinical characteristics of patients with JMML according to mutational status
24. JAK2 gene mutation is not a common event in JMML and is not involved in the pathogenesis of the disease
25. Essential thrombocythaemia in children in the Czech Republic
26. Case forum: Idiopathic myelofibrosis in children—Rare disease curable by bone marrow transplantation
27. Most pediatric patients with essential thrombocythemia show hypersensitivity to erythropoietin in vitro, with rare JAK2 V617F-positive erythroid colonies.
28. TEL/AML1 and immunoreceptor gene rearrangements-which comes first?
29. Prognostic value of structural chromosomal rearrangements and small cell clones with high hyperdiploidy in children with acute lymphoblastic leukemia.
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