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VITAMIN D STATUS IN THALASSEMIA MAJOR: AN UPDATE
2765PDF: 1095HTML: 2583 -
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
1280PDF: 740HTML: 212 -
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 -
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.
4308PDF: 1535HTML: 460 -
Hypophosphatemic osteomalacia associated with tenofovir: a multidisciplinary approach is required.
1391PDF: 851HTML: 10069cover letter to the editor: 170tile page: 252 -
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 -
ACQUIRED REFRACTORY IRON DEFICIENCY
3446PDF: 1153HTML: 1102 -
EXTREMELY OLD PATIENTS HOSPITALIZED IN INTERNAL MEDICINE: WHAT ABOUT THEIR ANEMIA? Anemia in the elderly
1633PDF: 516HTML: 247 -
Acquired Sideroblastic Anemia: An exploratory Comparative Statistical Analysis Between Clonal and Non-clonal cases Acquired Sideroblastic Anemia
995PDF: 603HTML: 403 -
IRON DEFICIENCY ANAEMIA AMONG PRE-SCHOOL CHILDREN WITH SICKLE CELL ANAEMIA: STILL A RARE DIAGNOSIS?
1348PDF: 834HTML: 2936cover leer: 150 -
ULTRASOUND AS FIRST LINE STEP IN ANAEMIA DIAGNOSTICS
1415PDF: 899HTML: 1857 -
Tuberculosis after gastrectomy, plasmatic concentration of antitubercular drugs
1605PDF: 796HTML: 824tile page: 168Table 1: 170 -
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An unusual cause of anemia and encephalopathy
3990PDF: 870HTML: 1519 -
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GROUP-BASED TRAJECTORY MODELING OF PLATELET IN PATIENTS WITH APLASTIC ANEMIA: A STUDY BASED ON THE MIMIC DATABASE
1026PDF: 1015Suppl. Files: 643HTML: 149 -
CLINICAL ASPECTS OF UNCOMPLICATED AND SEVERE MALARIA
8061PDF: 4258HTML: 7512 -
Anemia in the elderly: not always what it seems.
3334PDF: 1081HTML: 1785Figure 1: 186Figure 1 revised: 186 -
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
408PDF: 376Suppl. Files: 53HTML: 26 -
THE HISTORY OF DEFERIPRONE (L1) AND THE COMPLETE TREATMENT OF IRON OVERLOAD IN THALASSAEMIA The history and roles of deferiprone
2449PDF: 1606HTML: 654 -
Parvovirus B19-triggered acute hemolytic anemia and thrombocytopenia in a child with Evans syndrome
3554PDF: 1003HTML: 442Table 1.: 234 -
SYSTEMIC MASTOCYTOSIS: MULTIDISCIPLINARY APPROACH Systemic Mastocytosis
1590PDF: 1046HTML: 238 -
OMENTAL SPLENOSIS MIMICKING PERITONEAL CARCINOMATOSIS
154PDF: 172HTML: 21 -
DECREASED CD10 EXPRESSION IN THE BONE MARROW NEUTROPHILS OF HIV POSITIVE PATIENTS
1328PDF: 880HTML: 1158Coverletter: 222 -
THERAPEUTIC VALUE OF COMBINED THERAPY WITH DEFERASIROX AND SILYMARIN ON IRON OVERLOAD IN CHILDREN WITH BETA THALASSEMIA
2734PDF: 841HTML: 14970Therapeutic Value of Combined Therapy with Deferasirox and Silymarin on Iron Overload in Children with Beta Thalassemia: 322 -
HIGH SERUM ERYTHROPOIETIN AND FERRITIN LEVELS ASSOCIATED WITH ANEMIA RESPONSE IN MALIGNANT LYMPHOMA
1607PDF: 805HTML: 2862cover letter: 208 -
Parvovirus B19 infection in a patient with common variable immunodeficiency Parvovirus B19 infection in a patient with common variable immunodeficiency
1099PDF: 391HTML: 293







