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Parvovirus B19-triggered acute hemolytic anemia and thrombocytopenia in a child with Evans syndrome
3554PDF: 1002HTML: 438Table 1.: 234 -
SICKLE CELL ANAEMIA AND MALARIA
11569PDF: 7143HTML: 23926Figures Malaria and SCK: 219 -
ESCHERICHIA COLI: AN IMPORTANT PATHOGEN IN PATIENTS WITH HEMATOLOGIC MALIGNANCIES
1875PDF: 729HTML: 2119Untitled: 225Untitled: 158Untitled: 177Untitled: 161Untitled: 169Untitled: 184Untitled: 191 -
SPLANCHNIC VEIN THROMBOSIS IN THE MEDITERRANEAN AREA IN CHILDREN
2209PDF: 930HTML: 1656 -
PROPHYLAXIS OF MALARIA
3041PDF: 1046HTML: 17841Figures SChwartz: 172 -
A HEALTH RELATED QUALITY OF LIFE AND PSYCHOPATHOLOGICAL SYMPTOMS IN PEOPLE WITH HEMOPHILIA, BLOODBORNE CO-INFECTIONS AND COMORBIDITIES: AN ITALIAN MULTICENTER OBSERVATIONAL STUDY PSYCHOLOGICAL DINAMICS OF A GROUP OF ITALIAN HEMOPHILIACS WITH AND WITHOUT (CO)INFECTIONS AND COMORBIDITIES: A MULTICENTER STUDY
1533PDF: 1240HTML: 512 -
Severe autoimmune hemolytic anemia in Covid-19 infection Autoimmune hemolytic anemia in Covid-19
3263PDF: 1592HTML: 267 -
TREATMENT OF INDOLENT AND ADVANCED SYSTEMIC MASTOCYTOSIS Systemic Mastocytosis Treatment
2144PDF: 1552HTML: 513 -
PEDIATRIC MASTOCYTOSIS: AN UPDATE Chldren' Mastocytosis
1880HTML: 1482PDF: 1110 -
BACTERIAL INFECTIONS IN HEMATOPOIETIC STEM CELL TRANSPLANT RECIPIENTS
3209PDF: 1857HTML: 3673 -
Epstein-Barr Virus (EBV)-associated Haemophagocytic Syndrome
1869PDF: 848HTML: 1592 -
HEPATITIS B AND C IN HEMATOPOIETIC STEM CELL TRANSPLANT
995PDF: 542HTML: 729 -
LIVER IRON CONTENT IN INDIVIDUALS WITH LIVER IRON CONTENT IN INDIVIDUALS WITH Β-THALASSEMIA TRAIT AND HYPERFERRITINEMIA: ROLE OF METABOLIC ALTERATIONS, HFE GENOTYPES, AND CIRRHOSIS.: ROLE OF METABOLIC ALTERATIONS, HFE GENOTYPES, AND CIRRHOSIS. Β-THALASSEMIA TRAIT AND HYPERFERRITINEMIA
149PDF: 83Suppl. Files: 12HTML: 2 -
The Outcome of Six Patients with COVID-19 Infection and Multiple Myeloma. A Case Series and Literature Review COVID-19 in Multiple Myeloma patients
1006PDF: 369HTML: 208 -
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THE EFFECT OF ALPHA THALASSEMIA, HBF and HBC ON HAEMATOLOGICAL PARAMETERS OF SICKLE CELL DISEASE PATIENTS IN IBADAN, NIGERIA. ALPHA THALASSEMIA, HBF and HBC ON HAEMATOLOGICAL PARAMETERS OF SICKLE CELL DISEASE PATIENTS
2723PDF: 993HTML: 77 -
NEW THERAPEUTIC OPTIONS FOR THE TREATMENT OF SICKLE CELL DISEASE Guest Editor: Raffaella Origa
6901PDF: 3666HTML: 773 -
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PEDIATRIC TUBERCULOSIS IN THE NORTH SARDINIA
2497PDF: 880HTML: 2393 -
WHAT UNRELATED HEMATOPOIETIC STEM CELL TRANSPLANTATION IN THALASSEMIA TAUGHT US ABOUT TRANSPLANT IMMUNOGENETICS.
3178PDF: 1151HTML: 1502Untitled: 182Untitled: 175Untitled: 176 -
Measurement of erythrocyte lifespan using a CO breath test in patients with thalassemia and the impact of treatment erythrocyte lifespan in patients with thalassemia
779PDF: 556HTML: 174 -
ANTIBACTERIAL RESISTANCE IN PATIENTS WITH HEMATOPOIETIC STEM CELL TRANSPLANTATION
4115PDF: 1265HTML: 1963Table 1: 204 -
Severe eosinophilia in a case of giardiasis
1082PDF: 1579HTML: 430 -
GROWTH AND ENDOCRINE FUNCTION IN TUNISIAN THALASSEMIA MAJOR PATIENTS
2815PDF: 1033HTML: 423TABLE: 196FIGURES: 260







