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The New England Journal of Medicine, ISSN 0028-4793, 05/2013, Volume 368, Issue 19, pp. 1781 - 1790
Journal Article
Blood, ISSN 0006-4971, 04/2014, Volume 123, Issue 17, pp. 2645 - 2651
Journal Article
Leukemia, ISSN 0887-6924, 09/2013, Volume 27, Issue 9, pp. 1852 - 1860
Chronic myeloid malignancies are categorized to the three main categories myeloproliferative neoplasms (MPNs), myelodysplastic syndromes (MDSs) and MDS/MPN... 
monosomy 7 | MDS/MPN | SETBP1 | aCML | i(q10) | molecular marker | POLYCYTHEMIA-VERA | ACUTE MYELOID-LEUKEMIA | ESSENTIAL THROMBOCYTHEMIA | MOLECULAR MUTATIONS | ACTIVATING MUTATION | ONCOLOGY | CHRONIC MYELOPROLIFERATIVE DISORDERS | EXON 12 MUTATIONS | JAK2 | HEMATOLOGY | MYELODYSPLASTIC SYNDROMES | CHRONIC MYELOMONOCYTIC LEUKEMIA | Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative - diagnosis | Humans | Middle Aged | Male | Isochromosomes | Young Adult | Aged, 80 and over | Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative - genetics | Adult | Female | Nuclear Proteins - genetics | Chromosome Deletion | Proto-Oncogene Proteins c-cbl - genetics | Repressor Proteins - genetics | Mutation Rate | Myelodysplastic-Myeloproliferative Diseases - genetics | Chromosomes, Human, Pair 7 | Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative - mortality | Carrier Proteins - genetics | Myelodysplastic-Myeloproliferative Diseases - mortality | Myelodysplastic Syndromes - diagnosis | Myelodysplastic-Myeloproliferative Diseases - diagnosis | Bone Marrow - pathology | Myelodysplastic Syndromes - mortality | Aged | Myelodysplastic Syndromes - genetics | Mutation | Gene mutations | Physiological aspects | Genetic aspects | Research | Binding proteins | Myelodysplastic syndromes | Risk factors | Myeloproliferative disorders
Journal Article
Cancer, ISSN 0008-543X, 02/2017, Volume 123, Issue 3, pp. 459 - 467
BACKGROUND The introduction of novel prognostic factors such as minimal residual disease (MRD) and genomic profiling has led to the reevaluation of the role of... 
hypodiploidy | minimal residual disease | cytogenetics | prognosis | acute lymphoblastic leukemia (ALL) | complex | ACUTE LYMPHOCYTIC-LEUKEMIA | REGIMEN | PHASE-2 | CHILDREN | THERAPY | ONCOLOGY | PREDICTORS | OUTCOMES | Neoplasm, Residual - pathology | Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative - diagnosis | Prognosis | Humans | Middle Aged | Male | Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative - drug therapy | Precursor Cell Lymphoblastic Leukemia-Lymphoma - drug therapy | Cytodiagnosis | Aged, 80 and over | Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative - genetics | Vincristine - administration & dosage | Adult | Female | Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative - pathology | Precursor Cell Lymphoblastic Leukemia-Lymphoma - pathology | Doxorubicin - administration & dosage | Treatment Outcome | Precursor Cell Lymphoblastic Leukemia-Lymphoma - diagnosis | Remission Induction | Cytarabine - administration & dosage | Neoplasm, Residual - genetics | Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics | Disease-Free Survival | Adolescent | Aged | Usage | Research | Doxorubicin | Vincristine | Risk factors | Chemotherapy | Cyclophosphamide | Cytogenetics | Dosage and administration | Acute lymphocytic leukemia | Drug therapy | Cancer | Dexamethasone | Profiling | Acute lymphatic leukemia | Hypodiploidy | Leukemia | Abnormalities | Minimal residual disease | Lymphatic leukemia | Multivariate analysis | Patients | Survival | Philadelphia chromosome | Medical prognosis | Adults | Triploidy | Pretreatment
Journal Article
Journal Article