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CLINICAL AND LABORATORY FEATURES OF SICKLE CELL DISEASE S/D PUNJAB: IMPACT OF HBF AND HYDROXYUREA SCD S/D Punjab
1341PDF: 1154HTML: 123 -
COST OF HEMATOPOIETIC STEM CELL TRANSPLANTATION IN INDIA
2784PDF: 980HTML: 4710 -
Safety warning for ChAdOx1 nCov-19 vaccine in patients with sickle cell disease Astra Zeneca vaccine in Sickle cell disease (SCD)
2161PDF: 501HTML: 153 -
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DISTRIBUTION OF DNA DAMAGE REPAIR GENE POLYMORPHISM hOGG1, XRCC1 and p53 AMONG SICKLE CELL DISEASE PATIENTS IN INDIA
1574PDF: 795HTML: 1491Table Genotype and allele frequencies of hOGG1 codon 326 Ser>Cys and p53 72Arg>Pro polymorphisms among SCD patients and control group: 183 -
A case of iron deficiency anemia with co-existing Hb Fontainebleau.
1350PDF: 770HTML: 2074Untitled: 306 -
THERAPEUTIC GENE EDITING FOR HEMOGLOBINOPATHIES Gene therapy for Hemoglobinopathies.
2214PDF: 1327Html: 304 -
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SEROPOSITIVITY OF HEPATITIS B AND C AMONG SYRIAN MULTITRANSFUSED PATIENTS WITH HEMOGLOBINOPATHY
2982PDF: 757HTML: 1122Cover Letter: 205 -
IS HEMOGLOBIN E GENE WIDELY SPREAD IN THE STATE OF MADHYA PRADESH IN CENTRAL INDIA? EVIDENCE FROM FIVE TYPICAL FAMILIES
1421PDF: 883HTML: 7982Untitled: 203 -
Editorial : INTRODUCING MEDITERRANEAN JOURNAL OF HEMATOLOGY AND INFECTIOUS DISEASES
3358PDF: 588HTML: 674 -
SICKLE CELL ANAEMIA AND MALARIA
11584PDF: 7155HTML: 23959Figures Malaria and SCK: 220 -
The INFLUENCE OF NUTRITION ON DISEASE SEVERITY AND HEALTH-RELATED QUALITY OF LIFE IN ADULTS WITH SICKLE CELL DISEASE A Prospective Longitudinal Study
2418PDF: 949HTML: 326 -
Guest Editor: Raffaella Origa IRON TOXICITY AND HEMOPOIETIC CELL TRANSPLANTATION: TIME TO CHANGE THE PARADIGM. IRON TOXICITY AND HEMOPOIETIC CELL TRANSPLANTATION
1957PDF: 1229HTML: 250 -
SICKLE CELL DISEASE AND VENOUS THROMBOEMBOLISM
2296PDF: 912HTML: 2101 -
IRON DEFICIENCY ANAEMIA AMONG PRE-SCHOOL CHILDREN WITH SICKLE CELL ANAEMIA: STILL A RARE DIAGNOSIS?
1348PDF: 834HTML: 2936cover leer: 150 -
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
1214PDF: 957HTML: 463 -
Sickle cell disease and Bartonella spp. infection
1218PDF: 885HTML: 459 -
Major Artery Occlusion: a Rare Complication of Sickle Cell Disease
1382PDF: 1052HTML: 4615 -
Parvovirus B19-triggered acute hemolytic anemia and thrombocytopenia in a child with Evans syndrome
3554PDF: 1003HTML: 442Table 1.: 234 -
Aplastic anaemia with microfilaria in marrow aspirate
1585PDF: 813HTML: 1358 -
APLASTIC ANEMIA AND VIRAL HEPATITIS
1280PDF: 533HTML: 23090 -
PREVENTION OF POST-TRANSFUSION HEPATITIS BY SCREENING OF ANTIBODY TO HEPATITIS B CORE ANTIGEN IN HEALTHY BLOOD DONORS
1180PDF: 696HTML: 1256Title page: 210 -
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
2020PDF: 861HTML: 286 -
PREVALENCE OF SICKLE CELL TRAIT IN THE SOUTHERN SUBURBS OF BEIRUT, LEBANON
4159PDF: 1018HTML: 19179







