Search Results - "Kerbauy, J"
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Fludarabine induces apoptosis in chronic lymphocytic leukemia--the role of P53, Bcl-2, Bax, Mcl-1, and Bag-1 proteins
Published in Brazilian journal of medical and biological research (01-03-2006)“…The expression of P53, Bcl-2, Bax, Bag-1, and Mcl-1 proteins in CD5/CD20-positive B-chronic lymphocytic leukemia (B-CLL) cells from 30 typical CLL patients was…”
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Nephrotic syndrome as a clinical manifestation of graft-versus-host disease (GVHD) in a marrow transplant recipient after cyclosporine withdrawal
Published in Bone marrow transplantation (Basingstoke) (01-01-1999)“…GVHD is one of the most frequent complications of BMT and recently nephrotic syndrome (NS) has been described as a manifestation of chronic GVHD. Here, we…”
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3
Aberrant phenotypes in acute myeloid leukemia : A high frequency and clinical significance
Published in Haematologica (Roma) (01-08-2001)Get full text
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Fungal infections in marrow transplant recipients under antifungal prophylaxis with fluconazole
Published in Brazilian journal of medical and biological research (01-07-2002)“…Fungal infection is one of the most important causes of morbidity and mortality in bone marrow transplant (BMT) recipients. The growing incidence of these…”
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Acute promyelocytic leukemia: the study of t(15;17) translocation by fluorescent in situ hybridization, reverse transcriptase-polymerase chain reaction and cytogenetic techniques
Published in Brazilian journal of medical and biological research (01-06-2001)“…Acute promyelocytic leukemia (AML M3) is a well-defined subtype of leukemia with specific and peculiar characteristics. Immediate identification of t(15;17) or…”
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Karyotype of cryopreserved bone marrow cells
Published in Brazilian journal of medical and biological research (01-07-2003)“…The analysis of chromosomal abnormalities is important for the study of hematological neoplastic disorders since it facilitates classification of the disease…”
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Hyperhomocysteinemia increases the risk of venous thrombosis independent of the C677T mutation of the methylenetetrahydrofolate reductase gene in selected Brazilian patients
Published in Blood coagulation & fibrinolysis (01-04-2002)“…Fasting total homocysteine (tHcy) and the methylenetetrahydrofolate reductase (MTHFR) C677T mutation were evaluated in 91 patients with venous thromboembolism…”
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Effect of α‐thalassemia and β‐globin gene cluster haplotypes on the hematological and clinical features of sickle‐cell anemia in Brazil
Published in American journal of hematology (01-10-1996)“…To compare the features of sickle‐cell anemia in Brazil with those in other locales, we studied the effects of the β‐globin‐like gene cluster haplotype and…”
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The effect of unmodified or prestorage white cell-reduced allogeneic red cell transfusions on the immune responsiveness in orthopedic surgery patients
Published in Transfusion (Philadelphia, Pa.) (01-07-1999)“…BACKGROUND: The immunomodulatory effects of allogeneic blood transfusions have been attributed to the white cells (WBCs) present in the cellular blood…”
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The singular value of CD34 and CD117 expression for minimal residual disease detection in AML
Published in Leukemia research (01-11-2003)Get full text
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Post-Transplant Lymphoproliferative Disorders (PTLD) after Renal Transplantation: Management and Evolution of Seven Cases Among 1002 Renal Transplants in Sao Paulo, Brazil
Published in Leukemia & lymphoma (01-09-2000)“…We reported seven cases (0.7%) of PTLD among 1002 renal transplants performed at Renal Transplant Service from Hospital Sao Paulo - Universidade Federal de Sao…”
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Lack of Association Between N-ras Gene Mutations and Clinical Prognosis in Brazilian Children with Acute Lymphoblastic Leukemia
Published in Leukemia & lymphoma (2001)“…Point mutations in codons 12, 13 and 61 of the N-ras proto-oncogene have been detected in several human malignancies. We studied 170 patients with acute…”
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Zinc, copper and iron and their interrelations in the growth of sickle cell patients
Published in Archivos latinoamericanos de nutrición (01-09-1995)“…In this study we evaluated the nutritional status of 34 children with sickle cell disease (SS). Results were compared to 9 siblings with sickle cell trait (AS)…”
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14
Fluorescent in-situ hybridization (FISH) for BCR/ABL in chronic myeloid leukemia after bone marrow transplantation
Published in São Paulo medical journal (04-01-2001)“…Identification of Philadelphia chromosome or BCR/ABL gene rearrangement in chronic myeloid leukemia is important at diagnosis as well as after treatment. To…”
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Genetic Analysis of β-Thalassemia Major and β-Thalassemia Intermedia in Brazil
Published in Hemoglobin (01-01-1998)“…The development of methodologies to identify the molecular lesions responsible for different types of β-thalassemia has made it possible to correlate these…”
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Spinal cord compression in beta-thalassemia: follow-up after radiotherapy
Published in São Paulo medical journal (01-11-1998)“…Spinal cord compression due to extramedullary hematopoiesis is a well-described but rare syndrome encountered in several clinical hematologic disorders,…”
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Prognosis related to staging systems for chronic lymphocytic leukemia
Published in São Paulo medical journal (06-07-2000)“…Chronic lymphocytic leukemia (CLL) is a clonal lymphoproliferative disorder, characterized by B lymphocytic proliferation. CLL is the most frequent adult…”
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Clinical management of six cases of low-risk primary tonsillar non-Hodgkin's lymphoma
Published in São Paulo medical journal (02-09-1999)“…There have been many reports that favor aggressive systemic treatment with chemotherapy and radiotherapy, even for well-localized lymphomas, avoiding the need…”
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Prognostic factors in non-Hodgkin lymphomas
Published in São Paulo medical journal (06-01-2000)“…In Hodgkin's disease, each clinical or pathologic stage can be related to the extent of the area involved and predicts the next anatomical region at risk for…”
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Detection of trisomy 12 by fluorescent in situ hybridization (FISH) in chronic lymphocytic leukemia
Published in Genetics and molecular biology (01-09-2000)“…Chronic lymphocytic leukemia (CLL) presents a varying incidence of karyotypic abnormalities whose detection is complicated by difficulties in obtaining mitosis…”
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