535 results on '"Fonatsch, Christa"'
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2. Time-dependent changes in mortality and transformation risk in MDS
3. Akute myeloische Leukämien
4. Revised International Prognostic Scoring System for Myelodysplastic Syndromes
5. Detailed analysis of clonal evolution and cytogenetic evolution patterns in patients with myelodysplastic syndromes (MDS) and related myeloid disorders
6. Zytogenetische Diagnostik
7. Evidence for the Identity of Human Scatter Factor and Human Hepatocyte Growth Factor
8. Prolonged progression-free survival in patients with chronic lymphocytic leukemia receiving granulocyte colony-stimulating factor during treatment with fludarabine, cyclophosphamide, and rituximab
9. Meeting report: Vienna 2008 Workshop of the German–Austrian Working Group for Studying Prognostic Factors in Myelodysplastic Syndromes
10. Der Professorinnenclub der Medizinischen Universität Wien: Eine Initiative zur Förderung von Frauen und Frauennetzwerken in den medizinischen Wissenschaften
11. New insights into the prognostic impact of the karyotype in MDS and correlation with subtypes: evidence from a core dataset of 2124 patients
12. Idiopathic cytopenia of undetermined significance (ICUS) versus low risk MDS: The diagnostic interface
13. Tumor cytogenetics
14. Highly refractory acute myeloid leukemia
15. Relation of In Vitro Growth Characteristics to Cytogenetics and Treatment Outcome in Acute Myeloid Leukemia: Prognostic Significance in Patients with a Normal Karyotype
16. Results of a randomized double-blind placebo-controlled trial evaluating sequential high-dose cytosine arabinoside/mitoxantrone chemotherapy with or without granulocyte/macrophage-colony-stimulating factor in high-risk myelodysplastic syndromes
17. Nachruf Gebhard Flatz (1925–2019)
18. Functional PMS2 Hybrid Alleles Containing a Pseudogene-Specific Missense Variant Trace Back to a Single Ancient Intrachromosomal Recombination Event
19. The idic(X)(q13) in myeloid malignancies: breakpoint clustering in segmental duplications and association with TET2 mutations
20. High dose intermittent ARA-C (HiDAC) for consolidation of patients with de novo AML: a single center experience
21. Growing Evidence for an Underestimation of Poor-Risk Cytogenetics in the International Prognostic Scoring System in Myelodysplastic Syndromes
22. Overexpression of the paternally expressed gene 10 (PEG10) from the imprinted locus on chromosome 7q21 in high-risk B-cell chronic lymphocytic leukemia
23. Trisomy 1q42.3-qter and monosomy 21q22.3-qter associated with ear anomaly, facial dysmorphology, psychomotor retardation, and epilepsy: Delineation of a new syndrome
24. MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene
25. The human vigilin gene: identification, chromosomal localization and expression pattern
26. 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
27. 6-Thioguanine, Cytarabine, and Daunorubicin (TAD) and High-Dose Cytarabine and Mitoxantrone (HAM) for Induction, TAD for Consolidation, and Either Prolonged Maintenance by Reduced Monthly TAD or TAD-HAM-TAD and One Course of Intensive Consolidation by Sequential HAM in Adult Patients at All Ages With De Novo Acute Myeloid Leukemia (AML): A Randomized Trial of the German AML Cooperative Group
28. Morphologic Dysplasia in De Novo Acute Myeloid Leukemia (AML) Is Related to Unfavorable Cytogenetics but Has No Independent Prognostic Relevance Under the Conditions of Intensive Induction Therapy: Results of a Multiparameter Analysis From the German AML Cooperative Group Studies
29. Illegitimate splicing of the NF1 gene in healthy individuals mimics mutation-induced splicing alterations in NF1 patients
30. Chromosomal in situ hybridization of a Hodgkin's disease-derived cell line (L540) using DNA probes for TCRA, TCRB, MET, and rRNA
31. Interferon-α in Kombination oder Sequenz mit Chemotherapeutika zur Therapie der chronischen myeloischen Leukämie
32. Mutational and Expression Analysis of the NF1 Gene Argues Against a Role as Tumor Suppressor in Sporadic Pilocytic Astrocytomas
33. The leukaemia-associated transcription factors EVI-1 and MDS1/EVI1 repress transcription and interact with histone deacetylase
34. Cytogenetic risk groups in acute myeloblastic leukaemia differ greatly in their semi-solid colony growth
35. Patients with de novo acute myeloid leukaemia and complex karyotype aberrations show a poor prognosis despite intensive treatment: a study of 90 patients
36. Mapping of leukaemia-associated breakpoints in chromosome band 3q21 using a newly established PAC contig
37. Detection of chimeric BCR-ABL genes in acute lymphoblastic leukaemia by the polymerase chain reaction
38. Correlation of cytogenetic, molecular cytogenetic, and clinical findings in 59 patients with ANLL or MDS and abnormalities of the short arm of chromosome 12
39. Leading prognostic relevance of the BCR-ABL translocation in adult acute B-lineage lymphoblastic leukemia: a prospective study of the German Multicenter Trial Group and confirmed polymerase chain reaction analysis
40. Increased risk for therapy-associated hematologic malignancies in patients with carcinoma of the breast and combined homozygous gene deletions of glutathione transferases M1 and T1
41. The significance of trisomy 8 in de novo acute myeloid leukaemia: the accompanying chromosome aberrations determine the prognosis
42. Morphological and cytochemical findings in 150 cases of T-lineage acute lymphoblastic leukaemia in adults
43. Prognostic significance of additional chromosome abnormalities in adult patients with Philadelphia chromosome positive acute lymphoblastic leukaemia
44. Incidence and implication of additional chromosome aberrations in acute promyelocytic leukaemia with translocation t(15;17)(q22;q21): a report on 50 patients
45. The fusion of TEL and ABL in human acute lymphoblastic leukaemia is a rare event
46. Amplification of the AML1( CBFA2) gene on ring chromosomes in a patient with acute myeloid leukemia and a constitutional ring chromosome 21
47. Prognostic value of lactate dehydrogenase activity in myelodysplastic syndromes
48. Chromosomal Aberrations during Interferon Therapy for Chronic Myelogenous Leukemia
49. Computer aided analysis of additional chromosome aberrations in Philadelphia chromosome positive acute lymphoblastic leukaemia using a simplified computer readable cytogenetic notation
50. Editorial: Aktuelle Aspekte der Humangenetik
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