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Volumn 54, Issue 3, 2013, Pages 639-642
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Patients with therapy-related myelodysplastic syndromes and acute myeloid leukemia share genetic features but can be separated by blast counts and cytogenetic risk profiles into prognostically relevant subgroups
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Author keywords
[No Author keywords available]
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Indexed keywords
CD135 ANTIGEN;
HEMOGLOBIN;
MIXED LINEAGE LEUKEMIA PROTEIN;
NUCLEOPHOSMIN;
TRANSCRIPTION FACTOR RUNX1;
ACUTE GRANULOCYTIC LEUKEMIA;
ADULT;
AGED;
CANCER CHEMOTHERAPY;
CANCER PROGNOSIS;
CANCER RADIOTHERAPY;
CELL STRUCTURE;
CHROMOSOME BANDING PATTERN;
CLINICAL FEATURE;
COHORT ANALYSIS;
CYTOGENETICS;
FEMALE;
FLUORESCENCE IN SITU HYBRIDIZATION;
GENE MUTATION;
GENOTYPE;
HEMOGLOBIN BLOOD LEVEL;
HUMAN;
IMMUNOSUPPRESSIVE TREATMENT;
KARYOTYPE;
LETTER;
LEUKOCYTE COUNT;
MAJOR CLINICAL STUDY;
MALE;
MEDICAL HISTORY;
MUTATION RATE;
MYELODYSPLASTIC SYNDROME;
OUTCOME ASSESSMENT;
PRIORITY JOURNAL;
THROMBOCYTE COUNT;
ACUTE DISEASE;
ADOLESCENT;
ADULT;
AGED;
AGED, 80 AND OVER;
BLAST CRISIS;
CHEMORADIOTHERAPY;
CYTOGENETICS;
DIAGNOSIS, DIFFERENTIAL;
FEMALE;
HUMANS;
LEUKEMIA, MYELOID;
MALE;
MIDDLE AGED;
MYELODYSPLASTIC SYNDROMES;
PROGNOSIS;
RISK FACTORS;
SURVIVAL ANALYSIS;
YOUNG ADULT;
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EID: 84873381393
PISSN: 10428194
EISSN: 10292403
Source Type: Journal
DOI: 10.3109/10428194.2012.717275 Document Type: Letter |
Times cited : (12)
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References (9)
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