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THE SYSTEMIC MASTOCYTOSIS: RADIOLOGICAL POINT OF VIEW Systemic mastocytosis
1515PDF: 548HTML: 729 -
GROWTH AND ENDOCRINE FUNCTION IN TUNISIAN THALASSEMIA MAJOR PATIENTS
2776PDF: 1015HTML: 422TABLE: 192FIGURES: 254 -
ULTRASOUND AS FIRST LINE STEP IN ANAEMIA DIAGNOSTICS
1403PDF: 893HTML: 1834 -
EXERCISE STRESS ECHOCARDIOGRAPHY WITH TISSUE DOPPLER IMAGING (TDI) DETECTS EARLY SYSTOLIC DYSFUNCTION IN BETA-THALASSEMIA MAJOR PATIENTS WITHOUT CARDIAC IRON OVERLOAD
1338PDF: 813HTML: 7869Manuscript after revision: 243Barbero10328-36310-after revision: 233 -
THE HISTORY OF DEFERIPRONE (L1) AND THE COMPLETE TREATMENT OF IRON OVERLOAD IN THALASSAEMIA The history and roles of deferiprone
2421PDF: 1594HTML: 638 -
NON-SECRETORY MYELOMA: READY FOR A NEW DEFINITION?
3267PDF: 1712HTML: 1090 -
THE ROLE OF SERIAL RADIOGRAPHS TO DIAGNOSE DIABETIC FOOT BONE INFECTION. Serial radiographs and diabetic foot osteomyelitis
1412PDF: 704HTML: 212 -
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
848PDF: 604HTML: 207 -
SOLITARY PLASMACYTOMA
3878PDF: 2185HTML: 1234fIGURES 1,2: 220 -
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
41PDF: 32Suppl. Files: 4HTML: 0 -
DEFERASIROX: OVER A DECADE OF EXPERIENCE IN THALASSEMIA
2932PDF: 1597HTML: 237 -
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.
1303PDF: 727HTML: 329 -
CEREBRAL VENOUS THROMBOSIS IN THE MEDITERRANEAN AREA IN CHILDREN
2519PDF: 951HTML: 2236 -
MANAGEMENT OF PORTAL VEIN THROMBOSIS IN CIRRHOTIC PATIENTS
824PDF: 540HTML: 4026 -
MYELODYSPLASTIC SYNDROMES AND IRON CHELATION THERAPY
3396PDF: 1296HTML: 1908Fig.1: 201Fig. 2: 212 -
OMENTAL SPLENOSIS MIMICKING PERITONEAL CARCINOMATOSIS
127PDF: 155HTML: 19 -
Tacrolimus Associated Posterior Reversible Encephalopathy Syndrome – A Case Series and Review
3575PDF: 1505HTML: 4410CoverLetter: 185Figure1: 197 -
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
3128PDF: 1906HTML: 244 -
Lymphomatoid Granulomatosis of Central Nervous System and Lung Driven by Epstein Barr Virus Proliferation: Successful Treatment with Rituximab
1620PDF: 886HTML: 3157Figure 5: 155Figure 4: 158Figure 3: 192Figure 1: 172Figure 2: 168 -
Guest Editor: Pellegrino Musto REFINING HIGH-RISK MULTIPLE MYELOMA: ADVANCEMENTS IN GENOMIC, CLINICAL, AND PROGNOSTIC CRITERIA Multiple Myeloma High Risk Classificatio
2182PDF: 1596HTML: 305 -
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.
4283PDF: 1523HTML: 457 -
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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
1524PDF: 496HTML: 181 -
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
3938PDF: 1113HTML: 460 -
Takayasu Arteritis Initially Mimicking Infective Endocarditis
1288PDF: 603HTML: 1101 -
LATERAL SINUS THROMBOSIS IN OTOLOGY: A REVIEW
1599PDF: 948HTML: 4101Letter: 174 -
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
370PDF: 316Suppl. Files: 49HTML: 15 -
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
1731PDF: 547HTML: 167 -
Major Artery Occlusion: a Rare Complication of Sickle Cell Disease
1371PDF: 1045HTML: 4606







