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CLINICAL AND LABORATORY FEATURES OF SICKLE CELL DISEASE S/D PUNJAB: IMPACT OF HBF AND HYDROXYUREA SCD S/D Punjab
1477PDF: 1239HTML: 182 -
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Monocyte HLA-Dr Expression to Monitor Immune Response and Potential Infection Risks Following Vaso-Occlusive Crises in Patients with Sickle Cell Anemia Monocyte HLA-DR expression in SCA patients
896PDF: 633HTML: 298 -
Sickle cell disease and Bartonella spp. infection
1445PDF: 1472HTML: 531 -
Clinical and laboratory features of Hemoglobin La Desirade variant in association with sickle cell and alpha thalassemia genes Clinical & laboratory features of Hb La Desirade trait and compound heterozygous for Hb La Desirade and HbS Hemoglobin.
1979PDF: 568HTML: 399 -
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COAGULOPATHY IN BETA-THALASSEMIA: CURRENT UNDERSTANDING AND FUTURE PERSPECTIVES
1422PDF: 546HTML: 8370 -
Safety warning for ChAdOx1 nCov-19 vaccine in patients with sickle cell disease Astra Zeneca vaccine in Sickle cell disease (SCD)
2347PDF: 583HTML: 195 -
GROUP-BASED TRAJECTORY MODELING OF PLATELET IN PATIENTS WITH APLASTIC ANEMIA: A STUDY BASED ON THE MIMIC DATABASE
1165PDF: 1091Suppl. Files: 684HTML: 208 -
A strange case of Malaria in a Nigerian native boy.
2649PDF: 942HTML: 1346 -
THE HISTORY OF DEFERIPRONE (L1) AND THE COMPLETE TREATMENT OF IRON OVERLOAD IN THALASSAEMIA The history and roles of deferiprone
2764PDF: 1697HTML: 743 -
RELIABILITY OF DIFFERENT RBC INDICES AND FORMULAS IN DISCRIMINATING BETWEEN ?-THALASSEMIA MINOR AND OTHER CAUSES OF MICROCYTIC HYPOCHROMIC ANEMIA
3210PDF: 1714HTML: 14691Untitled: 273Untitled: 220 -
CLINICAL ASPECTS OF UNCOMPLICATED AND SEVERE MALARIA
8571PDF: 4615HTML: 7624 -
STUDY OF SERUM HAPTOGLOBIN LEVEL AND ITS RELATION TO ERYTHROPOIETIC ACTIVITY IN BETA THALASSEMIA CHILDREN .
2566PDF: 1257HTML: 2634Study of serum haptoglobin level in thalassemia: 463Figures: 287







