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PARASITIC INFECTIONS IN HEMATOPOIETIC STEM CELL TRANSPLANTATION
3651PDF: 1217HTML: 3872Untitled: 195Untitled: 244 -
CLINICAL AND LABORATORY FEATURES OF SICKLE CELL DISEASE S/D PUNJAB: IMPACT OF HBF AND HYDROXYUREA SCD S/D Punjab
1285PDF: 1111HTML: 102 -
TUBERCULOSIS IN PATIENTS WITH HAEMATOLOGICAL MALIGNANCIES
3198PDF: 1215HTML: 8094 -
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CIRCUMCISION IN MALES WITH BLEEDING DISORDERS
1880PDF: 879HTML: 6755Cover letter: 153 -
ZYGOMYCOSIS IN IMMUNOCOMPROMISED NON-HAEMATOLOGICAL PATIENTS
2772PDF: 918HTML: 7314 -
PERIOPERATIVE MANAGEMENT OF SICKLE CELL DISEASE: A NARRATIVE REVIEW
7887PDF: 3206HTML: 1197 -
DEFERASIROX: OVER A DECADE OF EXPERIENCE IN THALASSEMIA
2863PDF: 1564HTML: 222 -
MEDICAL TREATMENT OF HEPATOCELLULAR CARCINOMA
711PDF: 457HTML: 6254 -
THE HEMATOLOGICAL PARAMETERS AND BIOCHEMICAL MARKERS OF IRON STATUS IN ALFA-THALASSEMIA 3.7KB DELETION FROM METROPOLITAN REGION OF MANAUS, AMAZONAS, BRAZIL. alfa-Thalassemia 3.7 deletion From Amazonas, Brazil.
4067PDF: 587HTML: 353 -
ADVERSE PREGNANCY OUTCOMES IN SICKLE CELL TRAIT: A PROSPECTIVE COHORT STUDY EVALUATING CLINICAL AND HAEMATOLOGICAL PARAMETERS IN POSTPARTUM MOTHERS AND NEW-BORNS. Sickle cell trait pregnancy and outcomes
1317PDF: 1197HTML: 452 -
GENETIC HETEROGENEITY OF BETA GLOBIN MUTATIONS AMONG ASIAN-INDIANS AND IMPORTANCE IN GENETIC COUNSELLING AND DIAGNOSIS
1722PDF: 1267HTML: 11467Figure1: 161Figure 2: 162 -
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Sickle cell disease and Bartonella spp. infection
1126PDF: 847HTML: 443 -
SOCIOECONOMIC STATUS IS GLOBALLY A PROGNOSTIC FACTOR FOR OVERALL SURVIVAL OF MULTIPLE MYELOMA PATIENTS; SYNTHESIS OF STUDIES AND REVIEW OF THE LITERATURE SES as prognostic factor for myeloma survival
1991PDF: 803HTML: 203 -
IS IT POSSIBLE TO PREDICT TUMOR PROGRESSION THROUGH GENOMIC CHARACTERIZATION OF MONOCLONAL GAMMOPATHY AND SMOLDERING MULTIPLE MYELOMA? MONOCLONAL GAMMOPATHY AND SMOLDERING MULTIPLE MYELOMA
2517PDF: 1109HTML: 129 -
PATHOBIOLOGY OF HODGKIN LYMPHOMA
3149PDF: 1396HTML: 5836Fig1-Ag-Pil: 208Ag-Pil Fig.2: 215 -
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
9957PDF: 962HTML: 203 -
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.
4185PDF: 1499HTML: 436 -
Respiratory function in pediatric African SCA patients underwent bone marrow transplantation
2100PDF: 740HTML: 1027Spirometry in SCA patients before transplant: 192Spirometry in SCA patients post transplant: 171 -
EBV-RELATED LYMPHOPROLIFERATIVE DISEASES: A REVIEW IN LIGHT OF NEW CLASSIFICATIONS EBV-RELATED LYMPHOPROLIFERATIVE DISEASES
4040PDF: 1556HTML: 886







