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Rev. Bras. Hematol. Hemoter. vol.37 número2
... 6 reported the comparative results of metaphase cytogenetics and SNP-A in 25 Brazil- ian patients with diagnoses of AML or MDS; chromosomal abnormalities were detected in 40% and 68% of [r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.37 número2
... Autologous nonmyeloablative hematopoietic stem cell transplantation in patients with severe anti-TNF refractory Crohn disease: long-term follow-up. Hommes DW, Duijvestein M, Zelinkova Z,[r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.37 número2
... The clinical symptoms of hemolysis, hemoglobinuria and thrombosis were higher in the hemolytic forms of PNH (PNH/AA and Classic PNH) than in PNH-sc/AA (p-value < 0.001), whereas infec[r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.37 número2
... However, BCR-ABL/ABL transcript levels cannot be used as predictive estimates due to the lack of linearity of the ABL gene in assessing leukemic burden at levels above 10% and actual lev[r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.37 número2
... 4. Figueiredo MS, Kerbauy J, Gonc¸alves MS, Arruda VR, Saad St Sonati MF, et al. Effect of alpha-thalassemia and beta-globin gene cluster haplotypes on the and clinical features of sickle-cell anemia in Brazil. Am J ... See full document
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Rev. Bras. Hematol. Hemoter. vol.37 número2
... 5 Thus, due to differential treatment, the aim of this study was to report a case of hairy cell leukemia variant and cover some aspects related to the differential diagnosis between the [r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.37 número2
... 9. Santos EL, Tamegão-Lopes B, Machado LF, Ishak MO, Ishak R, Lemos JA, et al. Caracterizac¸ão molecular do HTLV-1/2 em doadores de sangue em Belém, Estado do Pará: primeira descric¸ão do subtipo HTLV-2b na região ... See full document
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Rev. Bras. Hematol. Hemoter. vol.37 número2
... During obstetric care, another morphological obstetric USG revealed a non-ectopic pregnancy with an echographic age of 19.1 weeks – in addition to an abdominal USG, which showed a solid [r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.37 número2
... Hemoglobin D-Punjab can be inherited in heterozygosis with hemoglobin A causing no clinical or hematological alterations, or in homozygosis, the rarest form of inheritance, a condition t[r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.37 número2
... The most common hematological abnormality of the SLE classification criteria in a cohort of Brazilian SLE patients was leukopenia followed by thrombocytopenia, lymphopenia and hemolytic [r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.37 número2
... Table 5 – The hypothetical hemoglobin concentration for poor performance status and hematopoietic cell transplantation-comorbidity index of patients with myeloid neoplasms. Groups HCT-CI[r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.37 número2
... Methods: Flow cytometry analysis of circulating endothelial cells was performed applying three different panels composed of different combinations of the CD144, CD146, CD31, CD133, CD45 [r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.37 número2
... This population sample includes patients with clinical suspicion of hemoglobinopathies and their family members, randomly chosen individuals who had blood tests and blood donors who were[r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.37 número2
... Conclusion: Physical therapy is efficient to treat musculoskeletal dysfunctions in sickle cell disease patients, irrespective of the technique; however, aquatic therapy showed a trend to[r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.37 número2
... IDA: iron deficiency anemia: -Thal: heterozygous beta-thalassemia; ACD combi: anemia of chronic disease associated with absolute iron deficiency; ACD: anemia of chronic disease; CG: con[r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.37 número2
... Evaluation of red cell and reticulocyte parameters as indicative of iron deficiency in patients with anemia of chronic disease. Rev Bras Hematol Hemoter[r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.37 número6
... Sequential monitoring of MRD using more sensitive and specific techniques, such as quantitative real-time poly- merase chain reaction (RQ-PCR) for immunoglobulin ( Ig ) and T-cell recept[r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.37 número6
... Therefore, this study does not support data published for patients without neutropenia; the CD64 index was not able to predict positive blood culture results in this specific popu- latio[r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.37 número6
... Intravenous iron sucrose versus oral iron supplementation for the treatment of iron deficiency anemia in patients with inflammatory bowel disease – a randomized, controlled, open-label, [r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.37 número6
... positive precursor B-cell acute lymphoblastic leukemia with positive minimal residual disease (0.32%) before conditioning treatment for hematopoietic stem cell transplantation.. In green[r] ... See full document
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