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MYELODYSPLASTIC SYNDROMES AND IRON CHELATION THERAPY
3886PDF: 1371HTML: 2180Fig.1: 271Fig. 2: 263 -
THE ROLE OF AUTOLOGOUS AND ALLOGENEIC STEM CELL TRANSPLANTATION IN FOLLICULAR LYMPHOMA IN THE NEW DRUGS ERA.
4214PDF: 1236HTML: 2120Fig.1: 248Fig. 2: 140Table 1: 252Table2: 274Table 3: 248 -
A case of iron deficiency anemia with co-existing Hb Fontainebleau.
1509PDF: 819HTML: 2106Untitled: 346 -
Cardiac toxicity associated with HCV direct antiviral agents Heart in HCV DAAs therapy
1699PDF: 1040HTML: 238 -
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HEPATITIS B AND C IN HEMATOPOIETIC STEM CELL TRANSPLANT
1061PDF: 573HTML: 750 -
NEW STRATEGIES FOR STEM CELL MOBILIZATION
2595PDF: 958HTML: 2584 -
Azacytidine failure revisited: an appraisal based on real life data from the MDS registry of the Hellenic Myelodysplastic Syndrome Study Group (HMDS). Azacytidine failure revisited
1300PDF: 948HTML: 353 -
Interstitial pneumonia triggered by H1N1 influenza A virus as the initial presentation of chronic myeloid leukemia
947PDF: 561HTML: 254Suppl. Files: 356 -
MILD BLEEDERS: DIAGNOSIS IS ELUSIVE IN LARGE NUMBER OF PATIENTS
3419PDF: 783HTML: 774Figure 1 Distribution of the various causes of mild bleeding (in %) in males and females: 241Figure 2 Age and Sex distribution of patients with Bleeding disorders- Unclassified: 244Table : Distribution of the sites of bleeding and their causes: 225 -
COMPARISON OF INFECTIOUS COMPLICATIONS IN PATIENTS RECEIVING HIGH-DOSE CYCLOPHOSPHAMIDE AS GVHD AFTER TRANSPLANTATION FROM A 9/10 HLA-MATCHED UNRELATED DONOR WITH STANDARD GVHD PROPHYLAXIS AFTER TRANSPLANT FROM A FULL MATCHING DONOR Infection With PTCy Versus Standard GvHD Prophylaxis
1565PDF: 1407HTML: 122 -
RECENT ADVANCES IN THE DEFINITION OF THE MOLECULAR ALTERATIONS OCCURRING IN MULTIPLE MYELOMA MOLECULAR ALTERATIONS OCCURRING IN MM
1401PDF: 1146HTML: 271 -
VIRAL HEPATITIS A TO E IN SOUTH MEDITERRANEAN COUNTRIES
1335PDF: 713HTML: 7780 -
THERAPEUTIC VALUE OF COMBINED THERAPY WITH DEFERASIROX AND SILYMARIN ON IRON OVERLOAD IN CHILDREN WITH BETA THALASSEMIA
2867PDF: 896HTML: 15034Therapeutic Value of Combined Therapy with Deferasirox and Silymarin on Iron Overload in Children with Beta Thalassemia: 376







