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COMPARISON OF IL-34, ELASTOGRAPHY, AND BIOPSY IN THE ASSESSMENT OF LIVER FIBROSIS IN CHRONIC HEPATITIS B Evaluating Non-Invasive and Invasive Methods in Liver Fibrosis
573PDF: 307Html: 27 -
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.
4311PDF: 1536HTML: 460 -
MEDICAL TREATMENT OF HEPATOCELLULAR CARCINOMA
744PDF: 474HTML: 6273 -
Improvement of liver involvement in familial Mediterranean fever after introduction of canakinumab: a case report Liver involvement in familial Mediterranean fever
1384PDF: 927HTML: 308 -
PATIENTS WITH HAEMOGLOBINOPATHIES AND CHRONIC HEPATITIS C: A REALLY DIFFICULT TO TREAT POPULATION IN 2016?
2960PDF: 994HTML: 2067Cover letter: 185 -
OUTLINE OF IRON METABOLISM, WITH EMPHASIS TO ERYTHROID CELLS iron Metabolism
2088PDF: 999Html: 352 -
VIRAL HEPATITIS A TO E IN SOUTH MEDITERRANEAN COUNTRIES
1267PDF: 652HTML: 7740 -
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Anemia in the elderly: not always what it seems.
3336PDF: 1083HTML: 1785Figure 1: 186Figure 1 revised: 187 -
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PATHOGENESIS OF MALARIA IN TISSUES AND BLOOD
4575PDF: 1946HTML: 17820 -
EBV-RELATED LYMPHOPROLIFERATIVE DISEASES: A REVIEW IN LIGHT OF NEW CLASSIFICATIONS EBV-RELATED LYMPHOPROLIFERATIVE DISEASES
4437PDF: 1734HTML: 1059 -
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DEFERASIROX: OVER A DECADE OF EXPERIENCE IN THALASSEMIA
2963PDF: 1603HTML: 239 -
LYMPHOPROLIFERATIVE SYNDROMES ASSOCIATED WITH HUMAN HERPESVIRUS-6A AND HUMAN HERPESVIRUS-6B
3797PDF: 1604HTML: 507Figures . Eliassian: 229 -
STUDY OF SERUM HAPTOGLOBIN LEVEL AND ITS RELATION TO ERYTHROPOIETIC ACTIVITY IN BETA THALASSEMIA CHILDREN .
2233PDF: 1178HTML: 2596Study of serum haptoglobin level in thalassemia: 352Figures: 185 -
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
417PDF: 384Suppl. Files: 53HTML: 27 -
THE HISTORY OF DEFERIPRONE (L1) AND THE COMPLETE TREATMENT OF IRON OVERLOAD IN THALASSAEMIA The history and roles of deferiprone
2457PDF: 1608HTML: 658 -
ACQUIRED REFRACTORY IRON DEFICIENCY
3459PDF: 1155HTML: 1104 -
GLUCOSE HOMEOSTASIS AND ΑSSESSMENT OF Β-CELL FUNCTION BY 3-HOUR ORAL GLUCOSE TOLERANCE (OGTT) IN PATIENTS WITH Β-THALASSEMIA MAJOR WITH SERUM FERRITIN BELOW 1,000 NG/DL: RESULTS FROM A SINGLE ICET-A CENTRE OGTT in thalassemia and iron overload
3976PDF: 1129HTML: 462 -
THE GUT MICROBIOTA AND IMMUNE SYSTEM RELATIONSHIP IN HUMAN GRAFT-VERSUS-HOST DISEASE
6375PDF: 2146HTML: 14033Untitled: 207figure: 191 -
HIV INFECTION, ANTIRETROVIRAL THERAPY AND CARDIOVASCULAR RISK
1907PDF: 809HTML: 3609 -
ULTRASOUND AS FIRST LINE STEP IN ANAEMIA DIAGNOSTICS
1420PDF: 901HTML: 1875 -
The INFLUENCE OF NUTRITION ON DISEASE SEVERITY AND HEALTH-RELATED QUALITY OF LIFE IN ADULTS WITH SICKLE CELL DISEASE A Prospective Longitudinal Study
2430PDF: 951HTML: 326 -
PROCALCITONIN AS A BIOMARKER OF BACTERIAL INFECTION IN SICKLE CELL VASO-OCCLUSIVE CRISIS.
2096PDF: 1063HTML: 15661COVER LETTER: 195 -
NEW THERAPEUTIC OPTIONS FOR THE TREATMENT OF SICKLE CELL DISEASE Guest Editor: Raffaella Origa
6937PDF: 3680HTML: 776 -
CLINICAL ASPECTS OF UNCOMPLICATED AND SEVERE MALARIA
8081PDF: 4263HTML: 7516 -
ASSESSMENT OF CONGENITAL NEUTROPENIA IN CHILDREN: COMMON CLINICAL SCENERIES AND CLUES FOR MANAGEMENT Assessment of congenital neutropenia in children
2335PDF: 1180HTML: 654







