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CLINICAL AND LABORATORY FEATURES OF SICKLE CELL DISEASE S/D PUNJAB: IMPACT OF HBF AND HYDROXYUREA SCD S/D Punjab
1375PDF: 1185HTML: 133 -
COST OF HEMATOPOIETIC STEM CELL TRANSPLANTATION IN INDIA
2820PDF: 996HTML: 4721 -
Safety warning for ChAdOx1 nCov-19 vaccine in patients with sickle cell disease Astra Zeneca vaccine in Sickle cell disease (SCD)
2203PDF: 525HTML: 168 -
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DISTRIBUTION OF DNA DAMAGE REPAIR GENE POLYMORPHISM hOGG1, XRCC1 and p53 AMONG SICKLE CELL DISEASE PATIENTS IN INDIA
1598PDF: 807HTML: 1527Table Genotype and allele frequencies of hOGG1 codon 326 Ser>Cys and p53 72Arg>Pro polymorphisms among SCD patients and control group: 190 -
A case of iron deficiency anemia with co-existing Hb Fontainebleau.
1418PDF: 782HTML: 2079Untitled: 314 -
THERAPEUTIC GENE EDITING FOR HEMOGLOBINOPATHIES Gene therapy for Hemoglobinopathies.
2264PDF: 1346Html: 318 -
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SEROPOSITIVITY OF HEPATITIS B AND C AMONG SYRIAN MULTITRANSFUSED PATIENTS WITH HEMOGLOBINOPATHY
3396PDF: 770HTML: 1124Cover Letter: 212 -
IS HEMOGLOBIN E GENE WIDELY SPREAD IN THE STATE OF MADHYA PRADESH IN CENTRAL INDIA? EVIDENCE FROM FIVE TYPICAL FAMILIES
1909PDF: 897HTML: 7988Untitled: 209 -
Editorial : INTRODUCING MEDITERRANEAN JOURNAL OF HEMATOLOGY AND INFECTIOUS DISEASES
3390PDF: 601HTML: 714 -
SICKLE CELL ANAEMIA AND MALARIA
11678PDF: 7226HTML: 24010Figures Malaria and SCK: 236 -
The INFLUENCE OF NUTRITION ON DISEASE SEVERITY AND HEALTH-RELATED QUALITY OF LIFE IN ADULTS WITH SICKLE CELL DISEASE A Prospective Longitudinal Study
2476PDF: 979HTML: 336 -
Guest Editor: Raffaella Origa IRON TOXICITY AND HEMOPOIETIC CELL TRANSPLANTATION: TIME TO CHANGE THE PARADIGM. IRON TOXICITY AND HEMOPOIETIC CELL TRANSPLANTATION
2000PDF: 1242HTML: 314 -
SICKLE CELL DISEASE AND VENOUS THROMBOEMBOLISM
2315PDF: 924HTML: 2201 -
IRON DEFICIENCY ANAEMIA AMONG PRE-SCHOOL CHILDREN WITH SICKLE CELL ANAEMIA: STILL A RARE DIAGNOSIS?
1479PDF: 846HTML: 2940cover leer: 159 -
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
1359PDF: 978HTML: 494 -
Sickle cell disease and Bartonella spp. infection
1335PDF: 1217HTML: 477 -
Major Artery Occlusion: a Rare Complication of Sickle Cell Disease
1403PDF: 1061HTML: 4665 -
Parvovirus B19-triggered acute hemolytic anemia and thrombocytopenia in a child with Evans syndrome
3598PDF: 1022HTML: 469Table 1.: 245 -
Aplastic anaemia with microfilaria in marrow aspirate
1606PDF: 829HTML: 1363 -
APLASTIC ANEMIA AND VIRAL HEPATITIS
1304PDF: 539HTML: 23120 -
PREVENTION OF POST-TRANSFUSION HEPATITIS BY SCREENING OF ANTIBODY TO HEPATITIS B CORE ANTIGEN IN HEALTHY BLOOD DONORS
1198PDF: 707HTML: 1270Title page: 220 -
PREVALENCE OF ANEMIA, IRON DEFICIENCY, AND IRON DEFICIENCY ANEMIA AND DIAGNOSTIC PERFORMANCE OF HEMATOLOGIC AND BIOCHEMICAL MARKERS OF SIDEROPENIA IN 1- TO 5-YEAR-OLD CHILDREN IN THRACE GREECE Prevalence of ID, IDA and anemia in Greek Thrace
2092PDF: 916HTML: 478 -
PREVALENCE OF SICKLE CELL TRAIT IN THE SOUTHERN SUBURBS OF BEIRUT, LEBANON
4187PDF: 1029HTML: 19208







