840 results on '"Haas, Oskar"'
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2. Risk factors in DUX4-positive childhood and adolescent B-cell acute lymphoblastic leukemia
3. Clinical characteristics and outcomes of B-cell precursor ALL with MEF2D rearrangements: a retrospective study by the Ponte di Legno Childhood ALL Working Group
4. Hyperdiploidy: the longest known, most prevalent, and most enigmatic form of acute lymphoblastic leukemia in children
5. Epigenetic regulator genes direct lineage switching in MLL/AF4 leukemia
6. Body‐wide chimerism and mosaicism are predominant causes of naturally occurring ABO discrepancies.
7. Clinical characteristics and outcomes of B-ALL with ZNF384 rearrangements: a retrospective analysis by the Ponte di Legno Childhood ALL Working Group
8. Retrospective identification of the first cord blood–transplanted severe aplastic anemia in a STAT1-associated chronic mucocutaneous candidiasis family: case report, review of literature and pathophysiologic background.
9. Genetic Predisposition to Non-Hodgkin Lymphoma
10. Hyperdiploid acute lymphoblastic leukemia in children with LZTR1 germline variants
11. A single‐center cohort study of patients with hereditary spherocytosis in Central Europe reveals a high frequency of novel disease‐causing genotypes
12. JAK2 p.G571S in B-cell precursor acute lymphoblastic leukemia: a synergizing germline susceptibility
13. Diagnostic Tool for the Identification of MLL Rearrangements Including Unknown Partner Genes
14. Optical Genome Mapping Identifies Novel Recurrent Structural Alterations in Childhood ETV6::RUNX1+ and High Hyperdiploid Acute Lymphoblastic Leukemia
15. The Human GRAF Gene Is Fused to MLL in a Unique t(5;11)(q31;q23) and Both Alleles Are Disrupted in Three Cases of Myelodysplastic Syndrome/Acute Myeloid Leukemia with a Deletion 5q
16. Use of HuH6 and other human-derived hepatoma lines for the detection of genotoxins: a new hope for laboratory animals?
17. Dominant inherited β‐thalassemia intermedia in a Polish family due to a novel frameshift mutation in HBB.
18. Resolving inherited and de novo germline predisposing sequence variants by means of whole exome trio analyses in childhood hematological malignancies
19. Deciphering the Somatic and Germline Structural Variation Landscape in Pediatric B-Cell Precursor Acute Lymphoblastic Leukemia By Whole Genome Optical Mapping
20. Clinical characteristics and outcomes of B-cell precursor ALL with MEF2D rearrangements: a retrospective study by the Ponte di Legno Childhood ALL Working Group
21. Band 3 nullVIENNA, a novel homozygous SLC4A1 p.Ser477X variant causing severe hemolytic anemia, dyserythropoiesis and complete distal renal tubular acidosis
22. Lmo2 expression defines tumor cell identity during T‐cell leukemogenesis
23. Genetik und genetische Prädisposition
24. Case Report: Refractory Cytopenia With a Switch From a Transient Monosomy 7 to a Disease-Ameliorating del(20q) in a NHEJ1-Deficient Long-term Survivor
25. Pediatric acute myeloid leukemia with t(8;16)(p11;p13), a distinct clinical and biological entity: a collaborative study by the International-Berlin-Frankfurt-Münster AML-study group
26. Epigenetic regulator genes direct lineage switching in MLL/AF4 leukemia
27. Small sizes and indolent evolutionary dynamics challenge the potential role of P2RY8-CRLF2–harboring clones as main relapse-driving force in childhood ALL
28. Perception and management of cancer predisposition in pediatric cancer centers: A European‐wide questionnaire‐based survey.
29. Comparative Genomic Hybridisation (CGH)
30. Genomics and drug profiling of fatal TCF3-HLF−positive acute lymphoblastic leukemia identifies recurrent mutation patterns and therapeutic options
31. DNA-Analysis by Flow-Cytometry of up to Nine Year Old Methanol/Acetic Acid Fixed Samples of Childhood Acute Lymphoblastic Leukemia (ALL)
32. Simultaneous Occurrence of t(8;21) and del(5q) in Myeloid Neoplasms
33. ETV6/RUNX1-positive relapses evolve from an ancestral clone and frequently acquire deletions of genes implicated in glucocorticoid signaling
34. Improved Outcome in Patients with Chronic Myelogenous Leukemia after Allogeneic Hematopoietic Stem Cell Transplantation Over the Past 25 Years: A Single-Center Experience
35. SARS-CoV-2 Infection and Active, Multiorgan, Severe cGVHD After HSCT for Adolescent ALL: More Luck Than Understanding? A Case Report
36. Chromosomal risk classification in high hyperdiploid acute lymphocytic leukaemia: the beginning of a new chapter
37. Development of treatment and clinical results in childhood AML in Austria (1993–2013)
38. Two Novel Missense Mutations and a 5bp Deletion in the Erythroid-Specific Promoter of the PKLR Gene in Two Unrelated Patients With Pyruvate Kinase Deficient Transfusion-Dependent Chronic Nonspherocytic Hemolytic Anemia
39. Molecular response to treatment redefines all prognostic factors in children and adolescents with B-cell precursor acute lymphoblastic leukemia: results in 3184 patients of the AIEOP-BFM ALL 2000 study
40. Chromosome 2q14.3 microdeletion encompassing CNTNAP5 gene in a patient carrying a complex chromosomal rearrangement
41. Copy Number Changes and Allele Distribution Patterns of Chromosome 21 in B Cell Precursor Acute Lymphoblastic Leukemia
42. Mastocytosis in AML-M2 with t(8;21) — a New Characteristic Association
43. Detection of AML1/ETO-Rearrangements in Acute Myeloid Leukemia with a Translocation t(8;21)
44. Somatic Sex: On the Origin of Neoplasms With Chromosome Counts in Uneven Ploidy Ranges
45. Epigenetic regulator genes direct lineage switching in MLL-AF4 leukaemia
46. Thiamine-responsive megaloblastic anemia (TRMA) in an Austrian boy with compound heterozygous SLC19A2 mutations
47. High-Hyperdiploid Acute Lymphoblastic Leukemia in Children with LZTR1 Germline Variants
48. Nanopore Cas9-Targeted Long-Read Sequencing - a Fast and Flexible Diagnostic Tool for the Identification of B-Cell Acute Lymphoblastic Leukemia Associated Gene Rearrangements
49. Cytogenetic features of acute lymphoblastic and myeloid leukemias in pediatric patients with Down syndrome: an iBFM-SG study
50. Mutations of JAK2 in acute lymphoblastic leukaemias associated with Down's syndrome
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