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THE SYSTEMIC MASTOCYTOSIS: RADIOLOGICAL POINT OF VIEW Systemic mastocytosis
1746PDF: 623HTML: 917 -
GROWTH AND ENDOCRINE FUNCTION IN TUNISIAN THALASSEMIA MAJOR PATIENTS
5882PDF: 1092HTML: 487TABLE: 233FIGURES: 321 -
ULTRASOUND AS FIRST LINE STEP IN ANAEMIA DIAGNOSTICS
1536PDF: 956HTML: 1995 -
EXERCISE STRESS ECHOCARDIOGRAPHY WITH TISSUE DOPPLER IMAGING (TDI) DETECTS EARLY SYSTOLIC DYSFUNCTION IN BETA-THALASSEMIA MAJOR PATIENTS WITHOUT CARDIAC IRON OVERLOAD
1433PDF: 864HTML: 7892Manuscript after revision: 285Barbero10328-36310-after revision: 283 -
THE HISTORY OF DEFERIPRONE (L1) AND THE COMPLETE TREATMENT OF IRON OVERLOAD IN THALASSAEMIA The history and roles of deferiprone
2686PDF: 1668HTML: 720 -
NON-SECRETORY MYELOMA: READY FOR A NEW DEFINITION?
3410PDF: 1782HTML: 1176 -
THE ROLE OF SERIAL RADIOGRAPHS TO DIAGNOSE DIABETIC FOOT BONE INFECTION. Serial radiographs and diabetic foot osteomyelitis
1679PDF: 792HTML: 278 -
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
2412PDF: 682HTML: 349 -
SOLITARY PLASMACYTOMA
4267PDF: 2275HTML: 1417fIGURES 1,2: 276 -
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
310PDF: 335Suppl. Files: 42HTML: 128 -
DEFERASIROX: OVER A DECADE OF EXPERIENCE IN THALASSEMIA
3280PDF: 1687HTML: 379 -
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.
1426PDF: 804HTML: 420 -
CEREBRAL VENOUS THROMBOSIS IN THE MEDITERRANEAN AREA IN CHILDREN
2593PDF: 1025HTML: 2260 -
MANAGEMENT OF PORTAL VEIN THROMBOSIS IN CIRRHOTIC PATIENTS
865PDF: 582HTML: 4041 -
MYELODYSPLASTIC SYNDROMES AND IRON CHELATION THERAPY
3866PDF: 1366HTML: 2178Fig.1: 268Fig. 2: 255 -
OMENTAL SPLENOSIS MIMICKING PERITONEAL CARCINOMATOSIS
225PDF: 214HTML: 36 -
Tacrolimus Associated Posterior Reversible Encephalopathy Syndrome – A Case Series and Review
3721PDF: 1624HTML: 4523CoverLetter: 245Figure1: 258 -
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
4233PDF: 2062HTML: 286 -
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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
1689PDF: 563HTML: 276 -
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
4104PDF: 1206HTML: 474 -
Lymphomatoid Granulomatosis of Central Nervous System and Lung Driven by Epstein Barr Virus Proliferation: Successful Treatment with Rituximab
1731PDF: 969HTML: 3198Figure 5: 195Figure 4: 196Figure 3: 232Figure 1: 212Figure 2: 208 -
Guest Editor: Pellegrino Musto REFINING HIGH-RISK MULTIPLE MYELOMA: ADVANCEMENTS IN GENOMIC, CLINICAL, AND PROGNOSTIC CRITERIA Multiple Myeloma High Risk Classificatio
2326PDF: 1699HTML: 686 -
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.
4436PDF: 1604HTML: 480 -
Takayasu Arteritis Initially Mimicking Infective Endocarditis
1423PDF: 646HTML: 1121 -
LATERAL SINUS THROMBOSIS IN OTOLOGY: A REVIEW
1713PDF: 1008HTML: 4200Letter: 211 -
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
593PDF: 611Suppl. Files: 80HTML: 168 -
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
1958PDF: 610HTML: 258 -
Major Artery Occlusion: a Rare Complication of Sickle Cell Disease
1434PDF: 1104HTML: 4676







