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VITAMIN D STATUS IN THALASSEMIA MAJOR: AN UPDATE
2711PDF: 1071HTML: 2566 -
ASSOCIATION OF VDBP RS4701 VARIANT, BUT NOT VDR/RXR-? OVER-EXPRESSION WITH BONE MINERAL DENSITY IN PEDIATRIC ?-THALASSEMIA PATIENTS Vitamin D metabolic axis and BMD in ?-thalassemia
1201PDF: 719HTML: 180 -
The INFLUENCE OF NUTRITION ON DISEASE SEVERITY AND HEALTH-RELATED QUALITY OF LIFE IN ADULTS WITH SICKLE CELL DISEASE A Prospective Longitudinal Study
2298PDF: 925HTML: 300 -
CONCISE REVIEW ON THE FREQUENCY, MAJOR RISK FACTORS AND SURVEILLANCE OF HEPATOCELLULAR CARCINOMA (HCC) IN ?-THALASSEMIAS: PAST, PRESENT AND FUTURE PERSPECTIVES Thalassaemia transfusion dependent, Hepatitis C, hepatocarcinoma.
4225PDF: 1513HTML: 444 -
Hypophosphatemic osteomalacia associated with tenofovir: a multidisciplinary approach is required.
1335PDF: 827HTML: 10044cover letter to the editor: 165tile page: 246 -
DISTRIBUTION OF DNA DAMAGE REPAIR GENE POLYMORPHISM hOGG1, XRCC1 and p53 AMONG SICKLE CELL DISEASE PATIENTS IN INDIA
1525PDF: 780HTML: 1475Table Genotype and allele frequencies of hOGG1 codon 326 Ser>Cys and p53 72Arg>Pro polymorphisms among SCD patients and control group: 178 -
EXTREMELY OLD PATIENTS HOSPITALIZED IN INTERNAL MEDICINE: WHAT ABOUT THEIR ANEMIA? Anemia in the elderly
1543PDF: 499HTML: 227 -
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Acquired Sideroblastic Anemia: An exploratory Comparative Statistical Analysis Between Clonal and Non-clonal cases Acquired Sideroblastic Anemia
942PDF: 577HTML: 336 -
IRON DEFICIENCY ANAEMIA AMONG PRE-SCHOOL CHILDREN WITH SICKLE CELL ANAEMIA: STILL A RARE DIAGNOSIS?
1306PDF: 821HTML: 2905cover leer: 144 -
ULTRASOUND AS FIRST LINE STEP IN ANAEMIA DIAGNOSTICS
1368PDF: 883HTML: 1806 -
Tuberculosis after gastrectomy, plasmatic concentration of antitubercular drugs
1575PDF: 775HTML: 811tile page: 160Table 1: 161 -
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An unusual cause of anemia and encephalopathy
3866PDF: 852HTML: 1507 -
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GROUP-BASED TRAJECTORY MODELING OF PLATELET IN PATIENTS WITH APLASTIC ANEMIA: A STUDY BASED ON THE MIMIC DATABASE
983PDF: 982Suppl. Files: 632HTML: 118 -
CLINICAL ASPECTS OF UNCOMPLICATED AND SEVERE MALARIA
7903PDF: 4091HTML: 7345 -
Anemia in the elderly: not always what it seems.
3301PDF: 1019HTML: 1774Figure 1: 173Figure 1 revised: 175 -
JUSTIFICATION OF UNIVERSAL IRON SUPPLEMENTATION FOR INFANTS 6-12 MONTHS IN REGIONS WITH A HIGH PREVALENCE OF THALASSEMIA Iron Supplementation for Infants 6-12 months in Regions with a High Prevalence of Thalassemia
2064PDF: 602Suppl. Files: 283HTML: 164 -
CEREBRAL VENOUS THROMBOSIS IN THE MEDITERRANEAN AREA IN CHILDREN
2503PDF: 942HTML: 2226 -
ANORECTAL PATHOLOGIES IN THE COURSE OF ACUTE LEUKAEMIAS: PREDICTIVE PARAMETERS Anorectal pathologies in leukemias
1166PDF: 717Html: 93 -
PATHOGENESIS OF MALARIA IN TISSUES AND BLOOD
4463PDF: 1914HTML: 17732 -
ASSESSMENT OF CONGENITAL NEUTROPENIA IN CHILDREN: COMMON CLINICAL SCENERIES AND CLUES FOR MANAGEMENT Assessment of congenital neutropenia in children
1972PDF: 1118HTML: 614 -
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AGING WITH THALASSEMIA AND SICKLE CELL DISEASE: A GERONTOLOGICAL MODEL OF ACCELERATED MULTIMORBIDITY AND FUNCTION-CENTERED CARE BEYOND MIDLIFE Thalassemia and Sickle Cell Diseases: Effect of Aging
283PDF: 224Suppl. Files: 41HTML: 8 -
THE HISTORY OF DEFERIPRONE (L1) AND THE COMPLETE TREATMENT OF IRON OVERLOAD IN THALASSAEMIA The history and roles of deferiprone
2390PDF: 1579HTML: 617 -
Parvovirus B19-triggered acute hemolytic anemia and thrombocytopenia in a child with Evans syndrome
3508PDF: 979HTML: 421Table 1.: 224 -
SYSTEMIC MASTOCYTOSIS: MULTIDISCIPLINARY APPROACH Systemic Mastocytosis
1506PDF: 933HTML: 220







