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HIGH SERUM ERYTHROPOIETIN AND FERRITIN LEVELS ASSOCIATED WITH ANEMIA RESPONSE IN MALIGNANT LYMPHOMA
1677PDF: 859HTML: 2881cover letter: 245 -
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THROMBOCYTOPENIA IN PATIENTS WITH CHRONIC HEPATITIS C VIRUS INFECTION
4379PDF: 2092HTML: 1972 -
Anemia in the elderly: not always what it seems.
3432PDF: 1153HTML: 1812Figure 1: 246Figure 1 revised: 261 -
COEXISTENCE OF MULTIPLE GENE VARIANTS IN SOME PATIENTS WITH ERYTHROCYTOSES Multiple gene variants in erythrocytosis
964PDF: 1312HTML: 161 -
NEW TREATMENTS FOR MYELODYSPLASTIC SYNDROMES
2124PDF: 1985HTML: 811 -
OUTLINE OF IRON METABOLISM, WITH EMPHASIS TO ERYTHROID CELLS iron Metabolism
2511PDF: 1392Html: 1104 -
THALIDOMIDE AMELIORATES ERYTHROPOIESIS AND IRON HOMEOSTASIS IN TRANSFUSION-DEPENDENT β-THALASSEMIA Thalidomide ameliorates erythropoiesis and iron homeostasis
1539PDF: 1506PDF: 1101HTML: 237 -
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JUSTIFICATION OF UNIVERSAL IRON SUPPLEMENTATION FOR INFANTS 6-12 MONTHS IN REGIONS WITH A HIGH PREVALENCE OF THALASSEMIA Iron Supplementation for Infants 6-12 months in Regions with a High Prevalence of Thalassemia
3434PDF: 673Suppl. Files: 330HTML: 312 -
ULTRASOUND AS FIRST LINE STEP IN ANAEMIA DIAGNOSTICS
1548PDF: 963HTML: 2013 -
SARS-CoV-2 INFECTED PATIENTS: FROM A HEMATOLOGIST PERSPECTIVE COVID-19 and Hematology
1591PDF: 1028HTML: 453 -
Diagnosis of del(5q) MDS, 14 years after JAK-2 positive PV appearance: complete remission of both diseases with lenalidomide monotherapy
2955PDF: 819HTML: 1328Blood Count trend before and during lenalidomide treatment: 239Light micrograph of bone marrow biopsy of a patient with PV and 5q deletion: 239 -
MYELODYSPLASTIC SYNDROMES AND IRON CHELATION THERAPY
3895PDF: 1373HTML: 2188Fig.1: 274Fig. 2: 263 -
EXTREMELY OLD PATIENTS HOSPITALIZED IN INTERNAL MEDICINE: WHAT ABOUT THEIR ANEMIA? Anemia in the elderly
1867PDF: 596HTML: 319 -
STUDY OF SERUM HAPTOGLOBIN LEVEL AND ITS RELATION TO ERYTHROPOIETIC ACTIVITY IN BETA THALASSEMIA CHILDREN .
2497PDF: 1241HTML: 2624Study of serum haptoglobin level in thalassemia: 436Figures: 262 -
PATHOGENESIS OF MALARIA IN TISSUES AND BLOOD
4773PDF: 2051HTML: 18213 -
Peripheral Red Blood Cell Split Chimerism as a Consequence of Intramedullary Selective Apoptosis of Recipient Red Blood Cells in a Case of Sickle Cell Disease
1767PDF: 1069HTML: 1898Untitled: 251Untitled: 225 -
TREATMENT OF CANCER IN THE OLDER AGED PERSON
1276PDF: 883HTML: 3421 -
THERAPY-RELATED MYELOID MALIGNANCIES IN MYELOMA
2623PDF: 862HTML: 1756 -
GENETIC PATHWAYS LEADING TO THERAPY-RELATED MYELOID NEOPLASMS
2714PDF: 877HTML: 5392 -
PERIOPERATIVE MANAGEMENT OF SICKLE CELL DISEASE: A NARRATIVE REVIEW
10710PDF: 3375HTML: 1651 -
TOXICITIES ASSOCIATED WITH CAR-T CELL THERAPIES CAR-T Cell Toxicity
2661PDF: 1799HTML: 718 -
THERAPEUTIC VALUE OF COMBINED THERAPY WITH DEFERASIROX AND SILYMARIN ON IRON OVERLOAD IN CHILDREN WITH BETA THALASSEMIA
2872PDF: 897HTML: 15034Therapeutic Value of Combined Therapy with Deferasirox and Silymarin on Iron Overload in Children with Beta Thalassemia: 378 -
PERPHERAL BLOOD CELL MITOCHONDRIAL DYSFUNCTION IN MYELODYSPLASTIC SYNDROMECAN BE IMPROVED BY A COMBINATION OF COENZYME Q10 AND CARNITINE Blood cell mitochondrial dysfunction in myelodysplastic syndrome
1336PDF: 850HTML: 417 -
CAUSES OF ADULT SPLANCHNIC VEIN THROMBOSIS IN THE MEDITERRANEAN AREA
2775PDF: 1011HTML: 3735 -
Thalidomide treatment for thrombocytopenia secondary to hypersplenism in children with β-thalassemia major: a case series Thalidomide treatment for thrombocytopenia
985PDF: 799HTML: 278 -
DIAMOND BLACKFAN ANEMIA: A TERTIARY CARE CENTRE EXPERIENCE
2772PDF: 911HTML: 3612Diamond Blackfan Anemia: A Tertiary care centre experience: 378







