V R Arruda

Summary

Publications

  1. ncbi request reprint Prevalence of the prothrombin gene variant (nt20210A) in venous thrombosis and arterial disease
    V R Arruda
    Hematology Hemotherapy Center, State University of Campinas, Campinas SP, Brazil
    Thromb Haemost 78:1430-3. 1997
  2. ncbi request reprint Prevalence of the prothrombin gene variant 20210 G --> A among patients with myocardial infarction
    V R Arruda
    Hematology Hemotherapy Center, State University of Campinas, SP Brazil
    Cardiovasc Res 37:42-5. 1998
  3. ncbi request reprint Inherited risk factors for thrombophilia among children with Legg-Calvé-Perthes disease
    V R Arruda
    Hematology Hemotherapy Center, State University of Campinas, Campinas SP, Brazil
    J Pediatr Orthop 19:84-7. 1999
  4. ncbi request reprint Three novel mutations in the activin receptor-like kinase 1 (ALK-1) gene in hereditary hemorrhagic telangiectasia type 2 in Brazilian patients
    A M Assis
    Hemoglobin and Genome Laboratory, Hematology and Hemotherapy Center, State University of Campinas, UNICAMP, R Carlos Chagas, 480, Cidade Universitaria Zeferino Vaz, Campinas, SP, Brazil
    J Hum Genet 52:237-43. 2007
  5. ncbi request reprint Eleven novel mutations in the factor VIII gene from Brazilian hemophilia A patients
    V R Arruda
    Department of Internal Medicine, State University of Campinas, UNICAMP, SP, Brazil
    Blood 86:3015-20. 1995
  6. ncbi request reprint The impact of the search for thrombophilia risk factors among antiphospholipid syndrome patients with thrombosis
    M Torresan
    Hematology Hemotherapy Center, State University of Campinas, UNICAMP, SP, Brazil
    Blood Coagul Fibrinolysis 11:679-82. 2000
  7. ncbi request reprint Increased risk for acute myeloid leukaemia in individuals with glutathione S-transferase mu 1 (GSTM1) and theta 1 (GSTT1) gene defects
    V R Arruda
    Department of Internal Medicine, State University of Campinas, Campinas, Sao Paulo, Brazil
    Eur J Haematol 66:383-8. 2001

Collaborators

Detail Information

Publications7

  1. ncbi request reprint Prevalence of the prothrombin gene variant (nt20210A) in venous thrombosis and arterial disease
    V R Arruda
    Hematology Hemotherapy Center, State University of Campinas, Campinas SP, Brazil
    Thromb Haemost 78:1430-3. 1997
    ..These data support the hypothesis that the prothrombin variant is a risk factor for venous thrombosis and suggest that it may also be a risk factor for arterial disease...
  2. ncbi request reprint Prevalence of the prothrombin gene variant 20210 G --> A among patients with myocardial infarction
    V R Arruda
    Hematology Hemotherapy Center, State University of Campinas, SP Brazil
    Cardiovasc Res 37:42-5. 1998
    ..The aim of this study was to determine the prevalence of the prothrombin variant allele 20210A among survivors of myocardial infarction...
  3. ncbi request reprint Inherited risk factors for thrombophilia among children with Legg-Calvé-Perthes disease
    V R Arruda
    Hematology Hemotherapy Center, State University of Campinas, Campinas SP, Brazil
    J Pediatr Orthop 19:84-7. 1999
    ..2 vs. 2.6%: p = 0.64) was determined. These data suggest that in our population, the heterozygosity for factor V Leiden was the only inherited risk factor associated with the development of LCPD...
  4. ncbi request reprint Three novel mutations in the activin receptor-like kinase 1 (ALK-1) gene in hereditary hemorrhagic telangiectasia type 2 in Brazilian patients
    A M Assis
    Hemoglobin and Genome Laboratory, Hematology and Hemotherapy Center, State University of Campinas, UNICAMP, R Carlos Chagas, 480, Cidade Universitaria Zeferino Vaz, Campinas, SP, Brazil
    J Hum Genet 52:237-43. 2007
    ..We suggest the high rate of mutation detection and the small size of the ALK-1 gene make genomic sequencing a viable diagnostic test for HHT2...
  5. ncbi request reprint Eleven novel mutations in the factor VIII gene from Brazilian hemophilia A patients
    V R Arruda
    Department of Internal Medicine, State University of Campinas, UNICAMP, SP, Brazil
    Blood 86:3015-20. 1995
    ..This study shows that the methodology used is safe and rapid and has potential for detecting almost all of the genetic defects of the studied hemophilia A patients...
  6. ncbi request reprint The impact of the search for thrombophilia risk factors among antiphospholipid syndrome patients with thrombosis
    M Torresan
    Hematology Hemotherapy Center, State University of Campinas, UNICAMP, SP, Brazil
    Blood Coagul Fibrinolysis 11:679-82. 2000
    ..7%; P = 0.01), suggesting that prothrombin variant could increase the risk of thrombosis in patients with antiphospholipid syndrome...
  7. ncbi request reprint Increased risk for acute myeloid leukaemia in individuals with glutathione S-transferase mu 1 (GSTM1) and theta 1 (GSTT1) gene defects
    V R Arruda
    Department of Internal Medicine, State University of Campinas, Campinas, Sao Paulo, Brazil
    Eur J Haematol 66:383-8. 2001
    ..Both the GST mu 1 (GSTM1) and GST theta 1 (GSTT1) genes have a null variant allele in which the entire gene is absent. In this study, we tested whether null genotypes for the GSTM1 and GSTT1 genes altered the risks for MDS, AML and AA...