840 results on '"Haas, Oskar"'
Search Results
202. Treatment Response and Outcome in Childhood t(1;19)/TCF3-PBX1 Positive Acute Lymphoblastic Leukemia: A Report from the Austrian BFM Group.
203. No Evidence for Constitutively Activated FLT3 in Juvenile Myelo-Monocytic Leukemia.
204. Immunogenotype Changes Prevail in Relapses of Young Children with TEL-AML1-Positive Acute Lymphoblastic Leukemia and Derive Mainly from Clonal Selection
205. NUP98 Is Fused to Topoisomerase (DNA) IIβ 180 kDa (TOP2B) in a Patient with Acute Myeloid Leukemia with a New t(3;11)(p24;p15)
206. Genetische Diagnostik in der pädiatrischen Onkologie Genetic diagnosis in pediatric oncology
207. Seven Novel and Stable Translocations Associated with Oncogenic Gene Expression in Malignant Melanoma
208. EQUAL FREQUENCY OF TEL/AML1+ ACUTE LYMPHOBLASTIC LEUKEMIA IN CHILDREN WITH AND WITHOUT DOWN SYNDROME
209. EQUAL FREQUENCY OFTEL/AML1REARRANGEMENTS IN CHILDREN WITH ACUTE LYMPHOBLASTIC LEUKEMIA WITH AND WITHOUT DOWN SYNDROME
210. Diagnostic tool for the identification of MLL rearrangements including unknown partner genes
211. Clonal Changes Are Frequent in Relapsed TEL-AML1+ ALL and Predominate in Young Children.
212. The ERG Gene in Normal and Malignant Megakaryopoiesis.
213. A Novel DNA/RNA FISH X Inactivation Assay Reveals a Nonrandom, Ploidy-Dependent Acquisition of the Active and Inactive X Chromosomes in Childhood Hyperdiploid Acute Lymphoblastic Leukemia (ALL) and Non-Hodgkin Lymphoma (NHL).
214. Analyzing the MLL Recombinome.
215. Detection of Trisomy 8 in Donor-Derived Ph−Cells in a Patient with Ph+Chronic Myeloid Leukemia Successfully Treated with Imatinib (STI571) in Relapse after Allogeneic Transplantation
216. Normal bone marrow function over 6 years in a patient with dysplastic hematopoiesis and a complex karyotype
217. Molecular Disease Eradication is a Prerequisite for Long-term Remission in Patients with t(8;21) Positive Acute Myeloid Leukemia: a Single Center Study
218. Aneurysmal bone cyst: a hereditary disease?
219. Clonal variation of the immunogenotype in relapsed ETV6/RUNX1‐positive acute lymphoblastic leukemia indicates subclone formation during early stages of leukemia development
220. Genetic Testing for Familial Mediterranean Fever in Austria by Means of Reverse-Hybridization Teststrips
221. Quantitation of the sterol regulatory element-binding protein mRNA in mononuclear blood cells by competitive RT-PCR
222. DNA deamination enables direct PCR amplification of the cystatin B (CSTB) gene-associated dodecamer repeat expansion in myoclonus epilepsy type Unverricht-Lundborg
223. Heterogeneity of the 7q36 breakpoints in the t(7;12) involvingETV6 in infant leukemia
224. Burkitt lymphoma following splenic marginal zone lymphoma
225. Mutational analysis of the SOX9 gene in campomelic dysplasia and autosomal sex reversal: lack of genotype/phenotype correlations
226. Absence of SV40 in Austrian Tumors Correlates with Low Incidence of Mesotheliomas
227. Nondisjunction of chromosomes leading to hyperdiploid childhood B-cell precursor acute lymphoblastic leukemia is an early event during leukemogenesis
228. Hypofibrinolysis, Lipoprotein(a), and Plasminogen Activator Inhibitor
229. Treatment of chronic myelogenous leukemia with the tyrosine kinase inhibitor STI571 results in marked regression of bone marrow fibrosis
230. Variable prognostic value of FLT3 internal tandem duplications in patients with de novo AML and a normal karyotype, t(15;17), t(8;21) or inv(16)
231. Sporadic Versus Familial Medullary Thyroid Microcarcinoma
232. An ins(X;11)(q24;q23) fuses theMLLand theSeptin 6/KIAA0128gene in an infant with AML-M2
233. Biased distribution of chromosomal breakpoints involving the MLL gene in infants versus children and adults with t(4;11) ALL
234. Cytogenetic risk groups in acute myeloblastic leukaemia differ greatly in their semi‐solid colony growth
235. Multiplex reverse transcriptase–polymerase chain reaction screening in childhood acute myeloblastic leukemia
236. 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
237. Microdissection and reverse painting reveals a microdeletion 6(q26qter) in a de novo r(6) chromosome
238. Spectral Karyotyping (SKY) of Hematologic Malignancies.
239. Elevated Levels of Lipoprotein(a) in Familial Bone Marrow Edema Syndrome of the Hip
240. 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
241. Monitoring of minimal residual disease in patients with MLL–AF6‐positive acute myeloid leukaemia by reverse transcriptase polymerase chain reaction
242. The ?typical? immunophenotype of acute promyelocytic leukemia (APL-M3): Does it prove true for the M3-variant?
243. Presence of clone-specific antigen receptor gene rearrangements at birth indicates an in utero origin of diverse types of early childhood acute lymphoblastic leukemia
244. A novel mutation E179K of the MEN1 gene predisposes for multiple endocrine neoplasia-type 1 (MEN1)
245. t(7;12)(q36;p13), a new recurrent translocation involvingETV6 in infant leukemia
246. Generation of Dendritic Cells from Human Chronic Myelomonocytic Leukemia Cells in Fetal Calf Serum-Free Medium
247. CBFB/MYH11 fusion in a patient with AML-M4Eo and cytogenetically normal chromosomes 16
248. Prolonged Third Remission in a Patient With Acute Promyelocytic Leukemia After Consolidation Chemotherapy With Intermittent Intermediate Dose Ara-C and Maintenance With Intermittent all-transRetinoic Acid (ATRA)
249. Development of treatment and clinical results in childhood AML in Austria (1993-2013).
250. Heterogeneous TCR delta Vδ2-Dδ3 rearrangements and their relation to IgH and TCR gamma gene status in childhood B cell precursor leukaemias
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