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THALASSEMIA AND VENOUS THROMBOEMBOLISM
3029PDF: 1141HTML: 4675 -
Major Artery Occlusion: a Rare Complication of Sickle Cell Disease
1414PDF: 1077HTML: 4670 -
Guest Editor: G. Castaman AGING WITH HEMOPHILIA: THE CHALLENGE OF APPROPRIATE DRUG PRESCRIPTION Hemophilia and aging
2992PDF: 1493HTML: 321 -
Can Polycythemia Vera evolve from Acute Myeloid Leukemia? A Case Report Showing a Simultaneous Minor JAK2 V617F Mutated Clone, De novo polycythemia vera following AML remission
1791PDF: 828HTML: 301 -
ASSESSMENT OF THE EFFICACY OF PROCALCITONIN, C-REACTIVE PROTEIN AND ALBUMIN LEVELS-GUIDED ANTIBIOTICS USE IN SEPSIS
1019PDF: 602Html: 305Suppl. Files: 190 -
DISTRIBUTION OF DNA DAMAGE REPAIR GENE POLYMORPHISM hOGG1, XRCC1 and p53 AMONG SICKLE CELL DISEASE PATIENTS IN INDIA
1625PDF: 818HTML: 1529Table Genotype and allele frequencies of hOGG1 codon 326 Ser>Cys and p53 72Arg>Pro polymorphisms among SCD patients and control group: 197 -
WALDENSTROM’S MACROGLOBULINEMIA: AN UPDATE
7842PDF: 2482HTML: 2116Table 1.: 246Table 2.: 257Table 3.: 238Table 4.: 233 -
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PREVALENCE OF SICKLE CELL TRAIT IN THE SOUTHERN SUBURBS OF BEIRUT, LEBANON
4216PDF: 1039HTML: 19217 -
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Measurement of erythrocyte lifespan using a CO breath test in patients with thalassemia and the impact of treatment erythrocyte lifespan in patients with thalassemia
836PDF: 588HTML: 207







