45 results on '"Haas, Oskar"'
Search Results
2. A single‐center cohort study of patients with hereditary spherocytosis in Central Europe reveals a high frequency of novel disease‐causing genotypes
3. Single nucleotide polymorphism array‐based signature of low hypodiploidy in acute lymphoblastic leukemia
4. Transfer and loss of allergen‐specific responses via stem cell transplantation: A prospective observational study
5. Aneuploidy in children with relapsed B‐cell precursor acute lymphoblastic leukaemia: clinical importance of detecting a hypodiploid origin of relapse
6. Somatic mosaic monosomy 7 and UPD7q in a child with MIRAGE syndrome caused by a novel SAMD9 mutation
7. Targeted mutation screening of 292 candidate genes in 38 children with inborn haematological cytopenias efficiently identifies novel disease-causing mutations
8. Band 3 nullVIENNA, a novel homozygousSLC4A1p.Ser477X variant causing severe hemolytic anemia, dyserythropoiesis and complete distal renal tubular acidosis
9. Peripheral blood late mixed chimerism in leucocyte subpopulations following allogeneic stem cell transplantation for childhood malignancies: does it matter?
10. Two Novel Missense Mutations and a 5bp Deletion in the Erythroid-Specific Promoter of thePKLRGene in Two Unrelated Patients With Pyruvate Kinase Deficient Transfusion-Dependent Chronic Nonspherocytic Hemolytic Anemia
11. High‐resolution analysis of alterations in medullary thyroid carcinoma genomes
12. Acute monocytic leukaemia originating from MLL‐MLLT3‐positive pre‐B cells
13. Detection of prognostically relevant genetic abnormalities in childhood B-cell precursor acute lymphoblastic leukaemia: recommendations from the Biology and Diagnosis Committee of the International Berlin-Frankfürt-Münster study group
14. Identification of PML as novel PAX5 fusion partner in childhood acute lymphoblastic leukaemia
15. Molecular dissection of t(11;17) in acute myeloid leukemia reveals a variety of gene fusions with heterogeneous fusion transcripts and multiple splice variants
16. An unusual case of myelodysplastic syndrome with prolonged clonal stability, indolent clinical course over a decade, and spontaneous regression of AML in the terminal phase
17. Clonal variation of the immunogenotype in relapsed ETV6/RUNX1‐positive acute lymphoblastic leukemia indicates subclone formation during early stages of leukemia development
18. Heterogeneity of the 7q36 breakpoints in the t(7;12) involvingETV6 in infant leukemia
19. Philadelphia chromosome-positive mature B-cell (Burkitt cell) leukaemia
20. Low frequency of clonotypic Ig and T‐cell receptor gene rearrangements in t(4;11) infant acute lymphoblastic leukaemia and its implication for the detection of minimal residual disease
21. A highly specific and sensitive fluorescence in situ hybridization assay for the detection of t(4;11)(q21;q23) and concurrent submicroscopic deletions in acute leukaemias
22. An ins(X;11)(q24;q23) fuses theMLLand theSeptin 6/KIAA0128gene in an infant with AML-M2
23. Cytogenetic risk groups in acute myeloblastic leukaemia differ greatly in their semi‐solid colony growth
24. PBPC mobilization with chemotherapy and G–CSF in patients with chronic myeloid leukemia: quantification of bcr/abl‐positive cells by interphase fluorescence in situ hybridization and competitive PCR
25. Monitoring of minimal residual disease in patients with MLL–AF6‐positive acute myeloid leukaemia by reverse transcriptase polymerase chain reaction
26. The ?typical? immunophenotype of acute promyelocytic leukemia (APL-M3): Does it prove true for the M3-variant?
27. t(7;12)(q36;p13), a new recurrent translocation involvingETV6 in infant leukemia
28. CBFB/MYH11 fusion in a patient with AML-M4Eo and cytogenetically normal chromosomes 16
29. Mapping of the breakpoints on the short arm of chromosome 17 in neoplasms with an i(17q)
30. Promoter-specific methylation and expression alterations of igf2 and h19 are involved in human hepatoblastoma
31. Relapse of Philadelphia chromosome positive acute lymphoblastic leukaemia after marrow transplantation: sustained molecular remission after early and dose‐escalating infusion of donor leucocytes
32. Distinction between sporadic and hereditary medullary thyroid carcinoma (MTC) by mutation analysis of theRET proto-oncogene
33. Graft failure after donor leucocyte infusion in relapsed chronic myeloid leukaemia: successful treatment with cyclophosphamide and antithymocyte globulin followed by peripheral blood stem cell infusion
34. Lack of DNA synthesis among CD34 + cells in cord blood and in cytokine‐mobilized blood
35. Detection of numerical and structural chromosome abnormalities in pediatric germ cell tumors by means of interphase cytogenetics
36. Autoimmune-thrombocytopenia and sle in a patient with 5q-anomaly and deletion of the c-fms oncogene
37. Interphase cytogenetic study of childhood acute lymphoblastic leukemia
38. Prognostic significance of myeloid-associated antigen expression on blast cells in children with acute lymphoblastic leukemia
39. Minimal requirements for the diagnosis, classification, and evaluation of the treatment of childhood acute lymphoblastic leukemia (ALL) in the “BFM family” cooperative group
40. Acute megakaryocytic leukemia in children clinical, immunologic, and cytogenetic findings in two patients
41. Pure red cell aplasia as possible early manifestation of chronic myeloid leukemia
42. Duration of first remission as an indicator of long‐term survival in chronic myelogenous leukaemia
43. Poorly differentiated, neuron-specific enolase positive round cell tumor with two translocations t(11;22) and t(21;22)
44. Platelet-associated immunoglobulins IgG, IgM, IgA and complement C3 in immune and nonimmune thrombocytopenic disorders
45. Immune thrombocytopenia more than a year after allogeneic marrow transplantation due to antibodies against donor platelets with anti-PIA1specificity: evidence for a host-derived immune reaction
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