|
Volumn 53, Issue 9, 2012, Pages 1824-1827
|
Chronic eosinophilic leukemia with erythroblastic proliferation and the rare translocation t(8;9)(p22;p24) with PCM1JAK2 fusion gene: A distinct clinical, pathological and genetic entity with potential treatment target?
|
Author keywords
[No Author keywords available]
|
Indexed keywords
ALKALINE PHOSPHATASE;
BILIRUBIN;
CYTARABINE;
HYDROXYUREA;
LACTATE DEHYDROGENASE;
RECOMBINANT ALPHA INTERFERON;
RETICULIN;
ADULT;
ALKALINE PHOSPHATASE BLOOD LEVEL;
BASOPHIL;
BILIRUBIN BLOOD LEVEL;
BLOOD CELL COUNT;
BLOOD SAMPLING;
BONE MARROW BIOPSY;
CASE REPORT;
CELL PROLIFERATION;
CESAREAN SECTION;
CHROMOSOME ANALYSIS;
CHROMOSOME HIGH RESOLUTION BANDING ANALYSIS;
CHROMOSOME TRANSLOCATION 22;
CHRONIC LEUKEMIA;
CONTROLLED STUDY;
DRUG WITHDRAWAL;
ECHOGRAPHY;
ENZYME BLOOD LEVEL;
EOSINOPHIL;
EOSINOPHIL COUNT;
EOSINOPHILIC LEUKEMIA;
ERYTHROBLAST;
ERYTHROPOIESIS;
FEMALE;
FIBROSIS;
FOLLOW UP;
FUSION GENE;
GENE MUTATION;
GENETICS;
GESTATION PERIOD;
HEPATOMEGALY;
HEPATOSPLENOMEGALY;
HUMAN;
IMMUNOHISTOCHEMISTRY;
LETTER;
LEUKOCYTOSIS;
LYMPHOCYTE;
MONOCYTE;
NEUTROPHIL;
NORMOCHROMIC NORMOCYTIC ANEMIA;
PATHOLOGY;
PREGNANCY TERMINATION;
PRIORITY JOURNAL;
PROMYELOCYTE;
SPLENOMEGALY;
THROMBOCYTOPENIA;
ANTINEOPLASTIC AGENTS;
CELL PROLIFERATION;
CHROMOSOMES, HUMAN, PAIR 8;
CHROMOSOMES, HUMAN, PAIR 9;
CHRONIC DISEASE;
DIAGNOSIS, DIFFERENTIAL;
ERYTHROBLASTS;
FEMALE;
HUMANS;
HYDROXYUREA;
HYPEREOSINOPHILIC SYNDROME;
INFANT, NEWBORN;
INTERFERON-ALPHA;
ONCOGENE PROTEINS, FUSION;
PREGNANCY;
PREGNANCY COMPLICATIONS, HEMATOLOGIC;
PREGNANCY COMPLICATIONS, NEOPLASTIC;
TRANSLOCATION, GENETIC;
TREATMENT OUTCOME;
YOUNG ADULT;
|
EID: 84864971463
PISSN: 10428194
EISSN: 10292403
Source Type: Journal
DOI: 10.3109/10428194.2012.661856 Document Type: Letter |
Times cited : (9)
|
References (12)
|