Clinical characteristics of patients with chronic eosinophilic leukaemia (CEL) harbouring FIP1L1-PDGFRA fusion transcript - Results of Polish multicentre study
The hypereosinophilic syndrome: Analysis of fourteen cases with review of the literature
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A tyrosine kinase created by fusion of the PDGFRA and FIP1L1 genes as a therapeutic target of imatinib in idiopathic hypereosinophilic syndrome
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Design and standardization of PCR primers and protocols for detection of clonal immunoglobulin and T-cell receptor gene recombinations in suspect lymphoproliferations: Report of the BIOMED-2 Concerted Action BMH4-T98-3936
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The efficacy of imatinib mesylate in patients with FIP1L1-PDGFRα positive hypereosinophilic syndrome. Results of a multicenter prospective study
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Molecular characterization of the idiopathic hypereosinophilic syndorme (HES) in 35 French patients with normal conventional cytogenetics
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FIP1L1-PDGFRA in eosinophilic disorders: Prevalence in routine clinical practice, long-term experience with imatinib therapy, and a critical review of the literature
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Low-dose imatinib mesylate leads to rapid induction of major molecular response and achievement of complete molecular remission in FIP1L1-PDGFRA positive chronic eosinophilic leukemia
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A single weekly dose of imatinib is sufficient to induce and maintain remission of chronic eosinophilic leukemia in FIP1L1-PDGFRA-expressing patients
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