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Showing 1569–1584 of 2301 results
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Article: P10 The genetic landscape of the murine 5T models for multiple myeloma
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Article: P10 Translocation (12;22) with TEL-MN1 (ETV6-MN1) fusion transcript: a recurrent, but rare genetic abnormality in acute myeloid leukaemia: case report and review of the literature
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Article: P11 Blastic plasmacytoid dendritic cell neoplasm with skin, bone marrow and CNS involvement: a case report
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Article: P11 CHOLESTEROL-AND PALMITATE/OLEATE-ENRICHED DIETS INDUCE DISTINCT AORTA AND AORTIC VALVE CALCIFICATION IN RABBIT MODELS
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Article: P11 EFFECT OF UNFRACTIONATED HEPARIN AND LOW MOLECULAR WEIGHT HEPARIN ON THE MEASUREMENT OF PT WITH TWO STAGO PT REAGENTS
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Article: P11 Low-pass sequencing of plasma cell DNA and of circulating cell-free DNA for the detection of copy number aberrations and early response monitoring in multiple myeloma
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Article: P11 Sporadic late-onset nemaline myopathy after allogeneic stem cell transplantation for refractory hepatosplenic gammadelta lymphoma: a case report
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Article: P12 DEVELOPMENT OF AN EASY-TO-USE ADAMTS13 CONFORMATION ASSAY USING FIBER OPTIC SURFACE PLASMON RESONANCE TECHNOLOGY
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Article: P12 Diagnostic utility of the lymphoid screening tube for Ogata score calculation in MDS investigation
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Article: P12 SENSITIVITY OF THE NEW STAGO PT STA-NEOPTIMAL REAGENT FOR FACTOR DEFICIENCY ON STAGO STA-R EVOLUTION
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Article: P12 The glycan-binding galectin-1 is involved in osteoclast biology
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Article: P13 CLINICAL EXOMES AND MENDELIOME SCREENING FOR THE DIAGNOSIS OF INHERITED BLEEDING, THROMBOTIC AND PLATELET DISORDERS USE IN A CLINICAL DIAGNOSTIC SETTING IN BELGIUM
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Article: P13 In vitro generation of tumor antigen-specific T cells from patient and healthy donor stem cells
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Article: P13 Monoclonal Gammopathy of Undetermined Significance (MGUS) after kidney transplantation: prevalence and clinical significance
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Article: P13 THE VALUE OF LABORATORY SCREENING VS. CLINICAL JUDGMENT IN HIT DIAGNOSIS: EXPERIENCES IN THREE BELGIAN HOSPITALS
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Article: P14 Cyclic thrombocytopenia in a patient with polycythemia vera: a case report
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