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Parasitic hypereosinophilia in childhood: a diagnostic challenge
2479PDF: 784HTML: 266Figure 1: 148 -
DIAGNOSTIC UTILITY OF FLOW CYTOMETRY IN MYELODYSPLASTIC SYNDROMES.
4662PDF: 1742HTML: 2100 -
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TUBERCULOSIS IN TROPICAL AREAS AND IMMIGRANTS
3218PDF: 1273HTML: 6172 -
NF- ?B Essential Modulator Deficiency Leading to Disseminated Cutaneous Atypical Mycobacteria
1619PDF: 1059HTML: 10688Untitled: 163 -
Screening and genetic diagnosis of Hemoglobinopathies in Southern and Northern Europe: Two examples
1121PDF: 467HTML: 1147Amato1: 152Figure 2 A: Prospective (grey columns) versus retrospective prevention (black columns) among indigenous couples at risk (left) and immigrant couples (right). Among immigrant couples the prevention it is still largely retrospective, while for Italian coupl: 229jdoe, : 236Figure 2 b: Prospective (grey columns) versus retrospective prevention (black columns) among indigenous couples at risk (left) and immigrant couples (right). Among immigrant couples the prevention it is still largely retrospective, while for Italian coupl: 140 -
PERIPHERAL NERVOUS SYSTEM INVOLVEMENT IN LYMPHOPROLIFERATIVE DISORDERS
1689PDF: 848HTML: 359Fig1: 212Fig.2: 228Fig. 3: 159Fig. 5: 170Fig. 4: 197 -
PATHOBIOLOGY OF HODGKIN LYMPHOMA
3105PDF: 1376HTML: 5831Fig1-Ag-Pil: 195Ag-Pil Fig.2: 202 -
CHILDREN IN CORONAVIRUSES’ WONDERLAND: WHAT CLINICIANS NEED TO KNOW Corona virus and Children
1348PDF: 901HTML: 289 -
HOMOZYGOUS DELETION ALFA-THALASSEMIA AND HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN, TWO GENETIC FACTORS PREDICTIVE THE REDUCTION OF MORBIDITY AND MORTALITY DURING PREGNANCY IN SICKLE CELL PATIENTS . A REPORT FROM DEMOCRATIC REPUBLIC OF CONGO ALPHA THALASSEMIA AND HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN REDUCE MORBIDITY DURING PREGNANCY IN SICKLE CELL PATIENTS
9930PDF: 947HTML: 194 -
The INFLUENCE OF NUTRITION ON DISEASE SEVERITY AND HEALTH-RELATED QUALITY OF LIFE IN ADULTS WITH SICKLE CELL DISEASE A Prospective Longitudinal Study
2194PDF: 883HTML: 288 -
SIMILARITIES OF ELDERLY AND THERAPY-RELATED AML
3500PDF: 834HTML: 6695 -
COEXISTENCE OF MULTIPLE GENE VARIANTS IN SOME PATIENTS WITH ERYTHROCYTOSES Multiple gene variants in erythrocytosis
776PDF: 1194HTML: 116 -
IDENTİFİCATİON OF LEİSHMANİA TROPİCA FROM PEDİATRİC VİSCERAL LEİSHMANİASİS İN SOUTHERN MEDITERRANEAN REGION OF TURKEY. Molecular characterization of pediatric visceral leishmaniasis
922PDF: 662HTML: 211 -
A strange case of Malaria in a Nigerian native boy.
2378PDF: 832HTML: 1289 -
TDT Positive High-Grade Lymphoma with Myc, BCL2 And BCL6 Rearrangements: a Review of Diagnosis and Treatment TDT POSITIVE HIGH-GRADE LYMPHOMA WITH MYC, BCL2 AND BCL6 REARRANGEMENTS.
1590PDF: 706HTML: 457 -
TREATMENT OF ACUTE MYELOID LEUKEMIA WITH 20-30% BONE MARROW BLASTS
2738PDF: 979HTML: 5497 -
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PREVENTION OF ? THALASSEMIA IN NORTHERN ISRAEL - A COST-BENEFIT ANALYSIS.
2404PDF: 1114HTML: 11773 -
PEDIATRIC TUBERCULOSIS IN THE NORTH SARDINIA
2417PDF: 822HTML: 2366 -
APLASTIC ANEMIA AND VIRAL HEPATITIS
1215PDF: 514HTML: 22992 -
THERAPY-RELATED MYELOID NEOPLASMS: CONSIDERATIONS FOR PATIENTS’ CLINICAL EVALUATION. Clinical Evaluation of T-AML
1527PDF: 775HTML: 138 -
HEMOGLOBIN ANALYSIS IN THE FIRST YEAR OF LIFE
3390PDF: 988HTML: 3008 -
NON-SECRETORY MYELOMA: READY FOR A NEW DEFINITION?
3146PDF: 1683HTML: 1071 -
IMMUNOLOGICAL EVOLUTION OF A COHORT OF HIV-2 INFECTED PATIENTS: PECULIARITIES OF AN UNDERESTIMATED INFECTION HIV-2 INFECTED PATIENTS PECULIARITIES
932PDF: 584HTML: 215 -
FASTING PLASMA GLUCOSE LEVELS WITHIN THE HIGH NORMAL RANGE ARE ASSOCIATED WITH A SIGNIFICANTLY INCREASED RISK OF FUTURE DYSGLYCEMIA IN TRANSFUSION-DEPENDENT Β THALASSEMIA: A DECADE-LONG MULTICENTER RETROSPECTIVE ANALYSIS Higher normal fasting plasma glucose and glucose dysregulation in β- thalassemia
543PDF: 182Html: 24 -
CEREBRAL VENOUS THROMBOSIS IN THE MEDITERRANEAN AREA IN ADULTS
2204PDF: 733HTML: 1241







