[PDF] Top 20 Rev. Bras. Hematol. Hemoter. vol.36 número5
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Rev. Bras. Hematol. Hemoter. vol.36 número5
... Comitê de Doenc¸as Infecciosas Transmitidas por Transfusão, Associac¸ão Brasileira de Hematologia, Hemoterapia e Terapia Celular, Rio de Janeiro, RJ, Brazil.. The number of cases of Chik[r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.36 número5
... Conclusion: These results confirm the high frequency of BCR-ABL rearrangements and the low survival rate of adult Brazilian patients with acute lymphoblastic leukemia7. © 2014 Associac¸ã[r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.36 número5
... A total of 51 SCD patients were enrolled in this study: 36 (70.6%) with sickle cell anemia (SCA) or Hb SS and 15 (29.4%) with Hb SC disease. Overall, the mean age of the patients was 11.76 ± 3.69 years. The Hb SS ... See full document
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Rev. Bras. Hematol. Hemoter. vol.36 número5
... Detection of cytogenetic abnormalities in mature B-cell neoplasms: the value of cultures with.. different mitogens.[r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.36 número5
... After measuring enzyme levels and genotyping, all five patients affected by the disease in this family fall into the clinical classification of type 1 GD.. In the International Collabora[r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.36 número5
... ease, and a second related donor allogeneic hematopoietic stem cell transplantation.. was performed.[r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.36 número5
... Acute renal failure following allogeneic hematopoietic cell transplantation: incidence, outcome and risk factors. Saudi J Kidney Dis Transpl[r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.36 número5
... that the majority of oncological clinics located in areas with endemic L. chagasi infections continue to have difficulties in making a firm diagnosis of VL. The clinical manifestations o[r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.36 número5
... Eight-year clinical outcomes of long-term enzyme replacement therapy for 884 children with Gaucher Disease Type 1. Siebert M, Bock H, Michelin-Tirelli K, Coelho JC, Giugliani R, Saraiva-[r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.36 número5
... This study shows that despite the medical advances in recent decades, pregnancy is still associated with many clinical and obstetric complications in patients with SCD, resulting in a hi[r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.36 número5
... In SCD patients, increased mean cell volume and low fetal hemoglobin were reported in both genders and high total hemoglobin and high mean corpuscular hemoglobin concentration were obser[r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.36 número5
... e Hemoter- apia, Camilo-Araújo present an analysis of the frequency of S-globin haplotypes and alpha-thalassemia, and their influ- ence on clinical manifestations and the hematological profile of children with ... See full document
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Rev. Bras. Hematol. Hemoter. vol.36 número5
... Although increasing knowledge on the complex pathophysiology of the sickle vaso-occlusive process has enabled better characterization of the endothelial dysfunction in SCD and how differ[r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.36 número5
... was the relationship between megakaryocyte TGF  1 expression, MVD and bone marrow fibrosis, suggesting a possible mechanism by which increased levels of TGF  1 produced by megakaryocyt[r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.36 número5
... In the article “Are the review criteria for automated complete blood counts of the International Society of Laboratory Hemato- logy suitable for all hematology laboratories?”, published [r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.36 número6
... Two deaths (28.6%) occurred in patients with suspected primary hemophagocytic lymphohistiocytosis; one whose clinical picture was triggered by cytomegalovirus infection did not respond t[r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.36 número6
... Mutations that reflect defects in the Klotho gene expression may be implicated in the onset of osteonecrosis, pri- apism, and leg ulcers in patients with sickle cell disease, as a result[r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.36 número6
... Objective: The purpose of this study was to evaluate the effectiveness of mature red cell and reticulocyte parameters under three conditions: iron deficiency anemia, anemia of chronic di[r] ... See full document
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Rev. Bras. Hematol. Hemoter. vol.36 número6
... The frequency of acute toxicity related to HSCT, in this con- text represented by GI symptoms, was high however the high aggressiveness of allogeneic transplantation should be con- sidered. In this study, over 90% of the ... See full document
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Rev. Bras. Hematol. Hemoter. vol.36 número6
... The aim of the study was to evaluate the intestinal barrier function in leukemic patients prior to chemotherapy, by test- ing intestinal permeability by the determination of urinary lact[r] ... See full document
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