Elena M Faioni

Summary

Affiliation: University of Milan
Country: Italy

Publications

  1. ncbi Expression of endothelial protein C receptor and thrombomodulin in the intestinal tissue of patients with inflammatory bowel disease
    Elena M Faioni
    Hematology and Thrombosis Unit, Ospedale San Paolo
    Crit Care Med 32:S266-70. 2004
  2. ncbi Mutations in the thrombomodulin gene are rare in patients with severe thrombophilia
    Elena M Faioni
    Department of Internal Medicine, Angelo Bianchi Bonomi Haemophilia and Thrombosis Centre, I R C C S Maggiore Hospital, University of Milan, Via A di Rudin 8, 201458 Milan, Italy
    Br J Haematol 118:595-9. 2002
  3. ncbi c.301C > T (p.Arg101Cys): a novel mutation in the thrombin-sensitive region of protein S associated with a dysfunctional protein
    Franca Franchi
    A Bianchi Bonomi Hemophilia and Thrombosis Centre, University of Milan and Department of Medicine and Medical Specialties, IRCCS Maggiore Hospital, Mangiagalli and Regina Elena Foundation, Milan, Italy
    Thromb Haemost 96:381-3. 2006
  4. ncbi Review of clinical, biochemical and genetic aspects of combined factor V and factor VIII deficiency, and report of a new affected family
    Elena M Faioni
    DMCO, University of Milano and Hematology and Thrombosis Unit, Ospedale San Paolo, Via A Di Rudini, 8, 20142 Milan, Italy
    Thromb Res 112:269-71. 2003
  5. ncbi Association of factor V deficiency with factor V HR2
    Elena M Faioni
    Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, IRCCS Maggiore Hospital and Department of Internal Medicine, University of Milan, Italy
    Haematologica 89:195-200. 2004
  6. ncbi Molecular diversity and thrombotic risk in protein S deficiency: the PROSIT study
    Eugenia Biguzzi
    Angelo Bianchi Bonomi Hemophilia and Thrombosis Centre, Department of Internal Medicine and Dermatology, IRCCS Maggiore Hospital and University of Milan, Milan, Italy
    Hum Mutat 25:259-69. 2005
  7. ncbi The factor V HR2 haplotype and the risk of venous thrombosis: a meta-analysis
    Giancarlo Castaman
    Department of Hematology, San Bortolo Hospital, Vicenza, Italy
    Haematologica 88:1182-9. 2003
  8. ncbi A novel G-to-A mutation in the intron-N of the protein S gene leading to abnormal RNA splicing in a patient with protein S deficiency
    Giovanna D'Andrea
    Unità di Aterosclerosi e Trombosi IRCCS Casa Sollievo della Sofferenza, Viale Cappuccini, San Giovanni Rotondo, 71013 Foggia, Italy
    Haematologica 88:459-64. 2003
  9. ncbi Association of estrogen receptor-alpha genepolymorphisms with venous thrombosis
    Federico Lussana
    Haematologica 91:279-80. 2006
  10. ncbi Expression of endothelial protein C receptor and thrombomodulin in human coronary atherosclerotic plaques
    Piera Angelica Merlini
    Division of Cardiology, Niguarda Ca Granda Hospital, Milan, Italy
    Ital Heart J 5:42-7. 2004

Collaborators

Detail Information

Publications10

  1. ncbi Expression of endothelial protein C receptor and thrombomodulin in the intestinal tissue of patients with inflammatory bowel disease
    Elena M Faioni
    Hematology and Thrombosis Unit, Ospedale San Paolo
    Crit Care Med 32:S266-70. 2004
    ..The soluble forms of the receptors in plasma were measured...
  2. ncbi Mutations in the thrombomodulin gene are rare in patients with severe thrombophilia
    Elena M Faioni
    Department of Internal Medicine, Angelo Bianchi Bonomi Haemophilia and Thrombosis Centre, I R C C S Maggiore Hospital, University of Milan, Via A di Rudin 8, 201458 Milan, Italy
    Br J Haematol 118:595-9. 2002
    ..Considering the lack of a phenotype and the costly screening procedure, we recommend that thrombomodulin defects be sought only for research purposes...
  3. ncbi c.301C > T (p.Arg101Cys): a novel mutation in the thrombin-sensitive region of protein S associated with a dysfunctional protein
    Franca Franchi
    A Bianchi Bonomi Hemophilia and Thrombosis Centre, University of Milan and Department of Medicine and Medical Specialties, IRCCS Maggiore Hospital, Mangiagalli and Regina Elena Foundation, Milan, Italy
    Thromb Haemost 96:381-3. 2006
  4. ncbi Review of clinical, biochemical and genetic aspects of combined factor V and factor VIII deficiency, and report of a new affected family
    Elena M Faioni
    DMCO, University of Milano and Hematology and Thrombosis Unit, Ospedale San Paolo, Via A Di Rudini, 8, 20142 Milan, Italy
    Thromb Res 112:269-71. 2003
  5. ncbi Association of factor V deficiency with factor V HR2
    Elena M Faioni
    Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, IRCCS Maggiore Hospital and Department of Internal Medicine, University of Milan, Italy
    Haematologica 89:195-200. 2004
    ..Factor V HR2 is associated with a mild increase in the risk of venous thromboembolism although not all studies concur on this point...
  6. ncbi Molecular diversity and thrombotic risk in protein S deficiency: the PROSIT study
    Eugenia Biguzzi
    Angelo Bianchi Bonomi Hemophilia and Thrombosis Centre, Department of Internal Medicine and Dermatology, IRCCS Maggiore Hospital and University of Milan, Milan, Italy
    Hum Mutat 25:259-69. 2005
    ....
  7. ncbi The factor V HR2 haplotype and the risk of venous thrombosis: a meta-analysis
    Giancarlo Castaman
    Department of Hematology, San Bortolo Hospital, Vicenza, Italy
    Haematologica 88:1182-9. 2003
    ..The association of FV Leiden and HR2 haplotype seems not to increase significantly the risk of VTE carried by isolated heterozygosity for FV Leiden. However, well-designed clinical studies are needed to clarify this issue definitely...
  8. ncbi A novel G-to-A mutation in the intron-N of the protein S gene leading to abnormal RNA splicing in a patient with protein S deficiency
    Giovanna D'Andrea
    Unità di Aterosclerosi e Trombosi IRCCS Casa Sollievo della Sofferenza, Viale Cappuccini, San Giovanni Rotondo, 71013 Foggia, Italy
    Haematologica 88:459-64. 2003
    ..Hereditary protein S (PS) deficiency is a rare autosomal disorder of the coagulation pathway associated with familial thrombophilia...
  9. ncbi Association of estrogen receptor-alpha genepolymorphisms with venous thrombosis
    Federico Lussana
    Haematologica 91:279-80. 2006
    ..We studied the distribution of ERalpha polymorphisms in patients with deep vein thrombosis. PvuII PP and XbaI XX genotypes may be associated with an approximately 2-fold increased DVT risk of deep vein thrombosis in men...
  10. ncbi Expression of endothelial protein C receptor and thrombomodulin in human coronary atherosclerotic plaques
    Piera Angelica Merlini
    Division of Cardiology, Niguarda Ca Granda Hospital, Milan, Italy
    Ital Heart J 5:42-7. 2004
    ....