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Parasitic hypereosinophilia in childhood: a diagnostic challenge
2625PDF: 828HTML: 314Figure 1: 175 -
PREVALENCE OF ß-THALASSEMIA MUTATIONS AMONG NORTHEASTERN IRANIAN POPULATION AND THEIR IMPACTS ON HEMATOLOGICAL INDICES AND APPLICATION OF PRENATAL DIAGNOSIS, A SEVEN-YEARS STUDY
2453PDF: 981HTML: 401Supplementary table 1: 231Some of the mutation detection samples: 222 -
HEMATOLOGICAL ABNORMALITIES BEYOND LYMPHOCYTOSIS DURING INFECTIOUS MONONUCLEOSIS: EPSTEIN-BARR VIRUS-INDUCED THROMBOCYTOPENIA THROMBOCYTOPENIA DURING INFECTIOUS MONONUCLEOSIS
2196HTML: 570PDF: 1363 -
HODGKIN LYMPHOMA IN CHILDREN: A 16-YEAR EXPERIENCE AT THE CHILDREN’S WELFARE TEACHING HOSPITAL OF BAGHDAD, IRAQ
1064PDF: 947Suppl. Files: 605HTML: 97 -
Lenalidomide and temozolomide combination in a very elderly patient with CNS relapse of diffuse large b-cell lymphoma.
3507PDF: 1067HTML: 1010Figure 1: 192 -
LOW INCIDENCE RATE OF OPPORTUNISTIC AND VIRAL INFECTIONS DURING IMATINIB TREATMENT IN CHRONIC MYELOID LEUKEMIA PATIENTS IN EARLY AND LATE CHRONIC PHASE
1665PDF: 811HTML: 871jdoe, table 2 infections CML .doc: 205jdoe, table 1 infections CML .doc: 195 -
THE Co-Occurrence of Jak2/Calr-Positive Myeloproliferative Disorder and Bcr-Abl-Positive Chronic Myelogenous Leukaemia Treated with Combination of Tyrosine Kinase Inhibitors and Ruxolitinib. Dual Myeloid Disorder Treated with Two Drug Association
1107PDF: 1217HTML: 101 -
Skin Involvement in Primary Systemic Amyloidosis
1684PDF: 910HTML: 4389Figure 1. Photographs showing (a) enlarged tongue with (b) teeth marks over the lateral margin and (c, d) multiple, papular lesions over lower chest wall: 191Figure 2. Microphotograph showing pink eosinophilic homogenous material in the dermis, H&E X 20: 169Figure 3. Pink eosinophilic material showing pale orange positivity with Congo red stain: 193 -
NEW TREATMENTS FOR MYELODYSPLASTIC SYNDROMES
2021PDF: 988HTML: 704 -
Cytomorphology of Chimeric Antigen Receptor T-Cells (CAR-T)
1549PDF: 559HTML: 236 -
GENETIC HETEROGENEITY OF BETA GLOBIN MUTATIONS AMONG ASIAN-INDIANS AND IMPORTANCE IN GENETIC COUNSELLING AND DIAGNOSIS
1803PDF: 1309HTML: 11529Figure1: 182Figure 2: 187 -
EPIDEMIOLOGY, DIAGNOSIS AND TREATMENT OF ACUTE PROMYELOCYTIC LEUKEMIA IN CHILDREN: THE EXPERIENCE IN CHINA
2418PDF: 865HTML: 2167New table Chinese children with APL: 170 -
ADVANCED HODGKIN LYMPHOMA: A NEW ERA OF THERAPY
2163PDF: 1337HTML: 3508 -
CHIMERIC ANTIGEN RECEPTOR T CELLS FOR THE TREATMENT OF MULTIPLE MYELOMA CAR T Cells and Myeloma Treatment
1784PDF: 871HTML: 518 -
THE HISTORY OF DEFERIPRONE (L1) AND THE COMPLETE TREATMENT OF IRON OVERLOAD IN THALASSAEMIA The history and roles of deferiprone
2468PDF: 1613HTML: 664 -
Simultaneous dual pathology in lymph node
1681PDF: 714HTML: 7743Simultaneous dual pathology in lymph node: 181Simultaneous dual pathology in lymph node: 181Simultaneous dual pathology in lymph node: 157Simultaneous dual pathology in lymph node: 195Simultaneous dual pathology in lymph node: 183 -
CAR-T CELL THERAPY FOR T-CELL MALIGNANCIES CAR-T CELL FOR T-CELL MALIGNANCIES
2242PDF: 2074HTML: 203 -
Idiopathic pulmonary embolism in a case of severe family ANKRD26 thrombocytopenia
2225PDF: 851HTML: 938Patient’s family tree: 185 -
MOLECULAR PATHOGENESIS OF SECONDARY ACUTE PROMYELOCYTIC LEUKEMIA
2925PDF: 873HTML: 6538Untitled: 252Untitled: 204Untitled: 225Untitled: 232 -
TREATMENT OF ACUTE PROMYELOCYTIC LEUKEMIA WITH AIDA BASED REGIMEN
4021PDF: 765HTML: 1858 -
THERAPEUTIC VALUE OF COMBINED THERAPY WITH DEFERASIROX AND SILYMARIN ON IRON OVERLOAD IN CHILDREN WITH BETA THALASSEMIA
2763PDF: 847HTML: 14977Therapeutic Value of Combined Therapy with Deferasirox and Silymarin on Iron Overload in Children with Beta Thalassemia: 329 -
PREVENTION OF ? THALASSEMIA IN NORTHERN ISRAEL - A COST-BENEFIT ANALYSIS.
2828PDF: 1266HTML: 11813 -
Mantle cell lymphoma relapsing at the lymphedematous arm.
1727PDF: 709HTML: 3809 -
RECENT ADVANCES IN THE DEFINITION OF THE MOLECULAR ALTERATIONS OCCURRING IN MULTIPLE MYELOMA MOLECULAR ALTERATIONS OCCURRING IN MM
1288PDF: 1089HTML: 220 -
THE EFFECT OF ALPHA THALASSEMIA, HBF and HBC ON HAEMATOLOGICAL PARAMETERS OF SICKLE CELL DISEASE PATIENTS IN IBADAN, NIGERIA. ALPHA THALASSEMIA, HBF and HBC ON HAEMATOLOGICAL PARAMETERS OF SICKLE CELL DISEASE PATIENTS
2798PDF: 1011HTML: 81 -
SPLANCHNIC VEIN THROMBOSIS IN THE MEDITERRANEAN AREA IN CHILDREN
2223PDF: 933HTML: 1659







