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CLINICAL AND LABORATORY FEATURES OF SICKLE CELL DISEASE S/D PUNJAB: IMPACT OF HBF AND HYDROXYUREA SCD S/D Punjab
1332PDF: 1145HTML: 121 -
COST OF HEMATOPOIETIC STEM CELL TRANSPLANTATION IN INDIA
2701PDF: 970HTML: 4706 -
Safety warning for ChAdOx1 nCov-19 vaccine in patients with sickle cell disease Astra Zeneca vaccine in Sickle cell disease (SCD)
2134PDF: 491HTML: 133 -
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DISTRIBUTION OF DNA DAMAGE REPAIR GENE POLYMORPHISM hOGG1, XRCC1 and p53 AMONG SICKLE CELL DISEASE PATIENTS IN INDIA
1549PDF: 788HTML: 1486Table Genotype and allele frequencies of hOGG1 codon 326 Ser>Cys and p53 72Arg>Pro polymorphisms among SCD patients and control group: 181 -
A case of iron deficiency anemia with co-existing Hb Fontainebleau.
1339PDF: 759HTML: 2049Untitled: 304 -
THERAPEUTIC GENE EDITING FOR HEMOGLOBINOPATHIES Gene therapy for Hemoglobinopathies.
2162PDF: 1300Html: 286 -
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SEROPOSITIVITY OF HEPATITIS B AND C AMONG SYRIAN MULTITRANSFUSED PATIENTS WITH HEMOGLOBINOPATHY
2969PDF: 746HTML: 1120Cover Letter: 201 -
IS HEMOGLOBIN E GENE WIDELY SPREAD IN THE STATE OF MADHYA PRADESH IN CENTRAL INDIA? EVIDENCE FROM FIVE TYPICAL FAMILIES
1400PDF: 878HTML: 7957Untitled: 200 -
Editorial : INTRODUCING MEDITERRANEAN JOURNAL OF HEMATOLOGY AND INFECTIOUS DISEASES
3337PDF: 585HTML: 667 -
SICKLE CELL ANAEMIA AND MALARIA
11506PDF: 7018HTML: 23894Figures Malaria and SCK: 215 -
The INFLUENCE OF NUTRITION ON DISEASE SEVERITY AND HEALTH-RELATED QUALITY OF LIFE IN ADULTS WITH SICKLE CELL DISEASE A Prospective Longitudinal Study
2360PDF: 939HTML: 310 -
Guest Editor: Raffaella Origa IRON TOXICITY AND HEMOPOIETIC CELL TRANSPLANTATION: TIME TO CHANGE THE PARADIGM. IRON TOXICITY AND HEMOPOIETIC CELL TRANSPLANTATION
1934PDF: 1219HTML: 241 -
SICKLE CELL DISEASE AND VENOUS THROMBOEMBOLISM
2248PDF: 893HTML: 2097 -
IRON DEFICIENCY ANAEMIA AMONG PRE-SCHOOL CHILDREN WITH SICKLE CELL ANAEMIA: STILL A RARE DIAGNOSIS?
1328PDF: 830HTML: 2925cover leer: 147 -
HEMATOPOIETIC STEM CELL TRANSPLANTATION IN SEVERE PEDIATRIC SICKLE CELL DISEASE: OUTCOME AND LONG-TERM COMPLICATIONS, SAUDI EXPERIENCE AT KING FAISAL SPECIALIST HOSPITAL, RIYADH, SAUDI ARABIA HCT in in Severe Pediatric Sickle Cell Disease
1197PDF: 943HTML: 451 -
PERIOPERATIVE MANAGEMENT OF SICKLE CELL DISEASE: A NARRATIVE REVIEW
8376PDF: 3250HTML: 1237 -
Anemia in the elderly: not always what it seems.
3319PDF: 1073HTML: 1779Figure 1: 181Figure 1 revised: 182 -
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Sickle cell disease and Bartonella spp. infection
1179PDF: 872HTML: 458 -
Major Artery Occlusion: a Rare Complication of Sickle Cell Disease
1371PDF: 1041HTML: 4605 -
Parvovirus B19-triggered acute hemolytic anemia and thrombocytopenia in a child with Evans syndrome
3535PDF: 987HTML: 428Table 1.: 229 -
Aplastic anaemia with microfilaria in marrow aspirate
1573PDF: 796HTML: 1351 -
APLASTIC ANEMIA AND VIRAL HEPATITIS
1266PDF: 530HTML: 23077







