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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
626PDF: 373Html: 34 -
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.
4395PDF: 1569HTML: 472 -
MEDICAL TREATMENT OF HEPATOCELLULAR CARCINOMA
770PDF: 485HTML: 6286 -
Improvement of liver involvement in familial Mediterranean fever after introduction of canakinumab: a case report Liver involvement in familial Mediterranean fever
1465PDF: 948HTML: 426 -
PATIENTS WITH HAEMOGLOBINOPATHIES AND CHRONIC HEPATITIS C: A REALLY DIFFICULT TO TREAT POPULATION IN 2016?
3012PDF: 1014HTML: 2119Cover letter: 200 -
OUTLINE OF IRON METABOLISM, WITH EMPHASIS TO ERYTHROID CELLS iron Metabolism
2416PDF: 1334Html: 1004 -
VIRAL HEPATITIS A TO E IN SOUTH MEDITERRANEAN COUNTRIES
1312PDF: 684HTML: 7767 -
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Anemia in the elderly: not always what it seems.
3404PDF: 1122HTML: 1804Figure 1: 212Figure 1 revised: 209 -
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PATHOGENESIS OF MALARIA IN TISSUES AND BLOOD
4696PDF: 1999HTML: 18167 -
EBV-RELATED LYMPHOPROLIFERATIVE DISEASES: A REVIEW IN LIGHT OF NEW CLASSIFICATIONS EBV-RELATED LYMPHOPROLIFERATIVE DISEASES
4632PDF: 1794HTML: 1248 -
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DEFERASIROX: OVER A DECADE OF EXPERIENCE IN THALASSEMIA
3201PDF: 1668HTML: 368 -
LYMPHOPROLIFERATIVE SYNDROMES ASSOCIATED WITH HUMAN HERPESVIRUS-6A AND HUMAN HERPESVIRUS-6B
3874PDF: 1652HTML: 866Figures . Eliassian: 257 -
STUDY OF SERUM HAPTOGLOBIN LEVEL AND ITS RELATION TO ERYTHROPOIETIC ACTIVITY IN BETA THALASSEMIA CHILDREN .
2366PDF: 1207HTML: 2613Study of serum haptoglobin level in thalassemia: 388Figures: 213 -
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
540PDF: 578Suppl. Files: 73HTML: 161 -
THE HISTORY OF DEFERIPRONE (L1) AND THE COMPLETE TREATMENT OF IRON OVERLOAD IN THALASSAEMIA The history and roles of deferiprone
2544PDF: 1643HTML: 710 -
ACQUIRED REFRACTORY IRON DEFICIENCY
3696PDF: 1268HTML: 1463 -
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
4059PDF: 1184HTML: 470 -
THE GUT MICROBIOTA AND IMMUNE SYSTEM RELATIONSHIP IN HUMAN GRAFT-VERSUS-HOST DISEASE
6474PDF: 2207HTML: 14153Untitled: 224figure: 209 -
HIV INFECTION, ANTIRETROVIRAL THERAPY AND CARDIOVASCULAR RISK
1942PDF: 829HTML: 3690 -
ULTRASOUND AS FIRST LINE STEP IN ANAEMIA DIAGNOSTICS
1511PDF: 929HTML: 1965 -
The INFLUENCE OF NUTRITION ON DISEASE SEVERITY AND HEALTH-RELATED QUALITY OF LIFE IN ADULTS WITH SICKLE CELL DISEASE A Prospective Longitudinal Study
2535PDF: 997HTML: 372 -
PROCALCITONIN AS A BIOMARKER OF BACTERIAL INFECTION IN SICKLE CELL VASO-OCCLUSIVE CRISIS.
2148PDF: 1092HTML: 15737COVER LETTER: 215 -
NEW THERAPEUTIC OPTIONS FOR THE TREATMENT OF SICKLE CELL DISEASE Guest Editor: Raffaella Origa
7106PDF: 3765HTML: 816 -
CLINICAL ASPECTS OF UNCOMPLICATED AND SEVERE MALARIA
8255PDF: 4459HTML: 7570 -
ASSESSMENT OF CONGENITAL NEUTROPENIA IN CHILDREN: COMMON CLINICAL SCENERIES AND CLUES FOR MANAGEMENT Assessment of congenital neutropenia in children
2550PDF: 1232HTML: 1073







