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THE SYSTEMIC MASTOCYTOSIS: RADIOLOGICAL POINT OF VIEW Systemic mastocytosis
1425PDF: 519HTML: 668 -
GROWTH AND ENDOCRINE FUNCTION IN TUNISIAN THALASSEMIA MAJOR PATIENTS
2680PDF: 977HTML: 399TABLE: 171FIGURES: 214 -
ULTRASOUND AS FIRST LINE STEP IN ANAEMIA DIAGNOSTICS
1329PDF: 860HTML: 1762 -
EXERCISE STRESS ECHOCARDIOGRAPHY WITH TISSUE DOPPLER IMAGING (TDI) DETECTS EARLY SYSTOLIC DYSFUNCTION IN BETA-THALASSEMIA MAJOR PATIENTS WITHOUT CARDIAC IRON OVERLOAD
1267PDF: 782HTML: 7859Manuscript after revision: 228Barbero10328-36310-after revision: 215 -
THE HISTORY OF DEFERIPRONE (L1) AND THE COMPLETE TREATMENT OF IRON OVERLOAD IN THALASSAEMIA The history and roles of deferiprone
2275PDF: 1551HTML: 584 -
NON-SECRETORY MYELOMA: READY FOR A NEW DEFINITION?
3170PDF: 1684HTML: 1071 -
THE ROLE OF SERIAL RADIOGRAPHS TO DIAGNOSE DIABETIC FOOT BONE INFECTION. Serial radiographs and diabetic foot osteomyelitis
1287PDF: 663HTML: 196 -
COMPARATIVE STUDY ON THE MEASUREMENT OF LIVER T2* VALUES OF THALASSEMIA PATIENTS AND THE CLINICAL GRADING OF LIVER IRON CONCENTRATION BY DIFFERENT POST-PROCESSING SOFTWARE MEASUREMENT OF LIVER T2* VALUES OF THALASSEMIA
767PDF: 563HTML: 185 -
SOLITARY PLASMACYTOMA
3774PDF: 2135HTML: 1203fIGURES 1,2: 195 -
DEFERASIROX: OVER A DECADE OF EXPERIENCE IN THALASSEMIA
2785PDF: 1543HTML: 218 -
ENDOTHELIAL BIOMARKERS IN PATIENTS RECOVERED FROM COVID-19 ONE YEAR AFTER HOSPITAL DISCHARGE: A CROSS-SECTIONAL STUDY Endothelial biomarkers in COVID-19 recoverers one year after hospital discharge.
1201PDF: 700HTML: 294 -
CEREBRAL VENOUS THROMBOSIS IN THE MEDITERRANEAN AREA IN CHILDREN
2474PDF: 924HTML: 2217 -
MANAGEMENT OF PORTAL VEIN THROMBOSIS IN CIRRHOTIC PATIENTS
792PDF: 526HTML: 4005 -
MYELODYSPLASTIC SYNDROMES AND IRON CHELATION THERAPY
3326PDF: 1266HTML: 1850Fig.1: 183Fig. 2: 189 -
Tacrolimus Associated Posterior Reversible Encephalopathy Syndrome – A Case Series and Review
3480PDF: 1449HTML: 4301CoverLetter: 172Figure1: 178 -
THE ROLE OF WHITE BLOOD CELL COUNT IN PERIANAL PATHOLOGIES: A RETROSPECTIVE ANALYSIS OF HEMATOLOGIC MALIGNANCIES Role of white blood cell count in perianal pathologies
2530PDF: 1777HTML: 221 -
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.
4158PDF: 1492HTML: 431 -
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A A RETROSPECTIVE LONG-TERM STUDY ON AGE AT MENARCHE AND MENSTRUAL CHARACTERISTICS IN 85 YOUNG WOMEN WITH TRANSFUSION-DEPENDENT Β-THALASSEMIA (TDT) BORN BETWEEN 1965 AND 1995 Long-Term Study on Age at Menarche and Menstrual Characteristics in patients with TDT
1444PDF: 463HTML: 164 -
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
3823PDF: 1069HTML: 411 -
Lymphomatoid Granulomatosis of Central Nervous System and Lung Driven by Epstein Barr Virus Proliferation: Successful Treatment with Rituximab
1537PDF: 854HTML: 3144Figure 5: 147Figure 4: 148Figure 3: 181Figure 1: 160Figure 2: 153 -
Guest Editor: Pellegrino Musto REFINING HIGH-RISK MULTIPLE MYELOMA: ADVANCEMENTS IN GENOMIC, CLINICAL, AND PROGNOSTIC CRITERIA Multiple Myeloma High Risk Classificatio
2094PDF: 1535HTML: 248 -
Takayasu Arteritis Initially Mimicking Infective Endocarditis
1222PDF: 575HTML: 1085 -
LATERAL SINUS THROMBOSIS IN OTOLOGY: A REVIEW
1521PDF: 915HTML: 4075Letter: 158 -
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
83PDF: 36Suppl. Files: 15HTML: 4 -
GLUCOSE METABOLISM AND INSULIN RESPONSE TO ORAL GLUCOSE TOLERANCE TEST (OGTT) IN PREPUBERTAL PATIENTS WITH TRANSFUSION DEPENDENT Β-THALASSEMIA (TDT): A LONG-TERM RETROSPECTIVE ANALYSIS Long-term retrospective analysis of glucose homeostasis in children with transfusion dependent β-thalassemia
1523PDF: 503HTML: 150 -
Major Artery Occlusion: a Rare Complication of Sickle Cell Disease
1326PDF: 1015HTML: 4593







