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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Flora Peyvandi

UOS Dipartimentale per la Diagnosi e la Terapia delle Coagulopatie

A Bianchi Bonomi Hemophilia and Thrombosis Center

Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico

Università degli Studi di Milano and Luigi Villa Foundation

Italy

[email]@unimi.it

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Affiliations

  • UOS Dipartimentale per la Diagnosi e la Terapia delle Coagulopatie, A Bianchi Bonomi Hemophilia and Thrombosis Center, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Università degli Studi di Milano and Luigi Villa Foundation, Italy. 2010 - 2012
  • Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, IRCCS Maggiore Hospital, Mangiagalli and Regina Elena Foundation, University of Milan, Italy. 2002 - 2009
  • Laboratorio di Patologia Molecolare Applicata alla Clinica, Fondazione Luigi Villa, Milano, Italia. 2008
  • Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, Milan, Italy. 2002 - 2004
  • Hematology Section, Department of Medicine, VA Boston Healthcare System, Harvard Medical School, USA. 2001

References

  1. Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders. Peyvandi, F., Palla, R., Menegatti, M., Siboni, S.M., Halimeh, S., Faeser, B., Pergantou, H., Platokouki, H., Giangrande, P., Peerlinck, K., Celkan, T., Ozdemir, N., Bidlingmaier, C., Ingerslev, J., Giansily-Blaizot, M., Schved, J.F., Gilmore, R., Gadisseur, A., Benedik-Dolničar, M., Kitanovski, L., Mikovic, D., Musallam, K.M., Rosendaal, F.R. J. Thromb. Haemost. (2012) [Pubmed]
  2. Post-partum hemorrhage in women with rare bleeding disorders. Peyvandi, F., Menegatti, M., Siboni, S.M. Thromb. Res. (2011) [Pubmed]
  3. ADAMTS-13 assays in thrombotic thrombocytopenic purpura. Peyvandi, F., Palla, R., Lotta, L.A., Mackie, I., Scully, M.A., Machin, S.J. J. Thromb. Haemost. (2010) [Pubmed]
  4. Introduction. Rare bleeding disorders: general aspects of clinical features, diagnosis, and management. Peyvandi, F., Palla, R., Menegatti, M., Mannucci, P.M. Semin. Thromb. Hemost. (2009) [Pubmed]
  5. Results of an international, multicentre pharmacokinetic trial in congenital fibrinogen deficiency. Peyvandi, F. Thromb. Res. (2009) [Pubmed]
  6. ADAMTS13 and anti-ADAMTS13 antibodies as markers for recurrence of acquired thrombotic thrombocytopenic purpura during remission. Peyvandi, F., Lavoretano, S., Palla, R., Feys, H.B., Vanhoorelbeke, K., Battaglioli, T., Valsecchi, C., Canciani, M.T., Fabris, F., Zver, S., Réti, M., Mikovic, D., Karimi, M., Giuffrida, G., Laurenti, L., Mannucci, P.M. Haematologica (2008) [Pubmed]
  7. Rare bleeding disorders. Peyvandi, F., Cattaneo, M., Inbal, A., De Moerloose, P., Spreafico, M. Haemophilia (2008) [Pubmed]
  8. National and international registries of rare bleeding disorders. Peyvandi, F., Spreafico, M. Blood. Transfus (2008) [Pubmed]
  9. Mechanisms of the interaction between two ADAMTS13 gene mutations leading to severe deficiency of enzymatic activity. Peyvandi, F., Lavoretano, S., Palla, R., Valsecchi, C., Merati, G., De Cristofaro, R., Rossi, E., Mannuccio Mannucci, P. Hum. Mutat. (2006) [Pubmed]
  10. Genetic diagnosis of haemophilia and other inherited bleeding disorders. Peyvandi, F., Jayandharan, G., Chandy, M., Srivastava, A., Nakaya, S.M., Johnson, M.J., Thompson, A.R., Goodeve, A., Garagiola, I., Lavoretano, S., Menegatti, M., Palla, R., Spreafico, M., Tagliabue, L., Asselta, R., Duga, S., Mannucci, P.M. Haemophilia (2006) [Pubmed]
  11. Rare bleeding disorders. Peyvandi, F., Kaufman, R.J., Seligsohn, U., Salomon, O., Bolton-Maggs, P.H., Spreafico, M., Menegatti, M., Palla, R., Siboni, S., Mannucci, P.M. Haemophilia (2006) [Pubmed]
  12. Role of the 2 adenine (g.11293_11294insAA) insertion polymorphism in the 3' untranslated region of the factor VII (FVII) gene: molecular characterization of a patient with severe FVII deficiency. Peyvandi, F., Garagiola, I., Palla, R., Marziliano, N., Mannucci, P.M. Hum. Mutat. (2005) [Pubmed]
  13. Carrier detection and prenatal diagnosis of hemophilia in developing countries. Peyvandi, F. Semin. Thromb. Hemost. (2005) [Pubmed]
  14. Phenotype-genotype characterization of 10 families with severe a subunit factor XIII deficiency. Peyvandi, F., Tagliabue, L., Menegatti, M., Karimi, M., Komáromi, I., Katona, E., Muszbek, L., Mannucci, P.M. Hum. Mutat. (2004) [Pubmed]
  15. CYP2C9 genotypes and dose requirements during the induction phase of oral anticoagulant therapy. Peyvandi, F., Spreafico, M., Siboni, S.M., Moia, M., Mannucci, P.M. Clin. Pharmacol. Ther. (2004) [Pubmed]
  16. The P303T mutation in the human factor VII (FVII) gene alters the conformational state of the enzyme and causes a severe functional deficiency. Peyvandi, F., De Cristofaro, R., Garagiola, I., Palla, R., Akhavan, S., Landolfi, R., Mannucci, P.M. Br. J. Haematol. (2004) [Pubmed]
  17. Gene mutations and three-dimensional structural analysis in 13 families with severe factor X deficiency. Peyvandi, F., Menegatti, M., Santagostino, E., Akhavan, S., Uprichard, J., Perry, D.J., Perkins, S.J., Mannucci, P.M. Br. J. Haematol. (2002) [Pubmed]
  18. Two naturally occurring mutations on FVII gene (S363I-W364C) altering intrinsic catalytic activity. Peyvandi, F., De Cristofaro, R., Akhavan, S., Carew, J.A., Landolfi, R., Bauer, K.A., Mannucci, P.M. Thromb. Haemost. (2002) [Pubmed]
  19. Abnormal secretion and function of recombinant human factor VII as the result of modification to a calcium binding site caused by a 15-base pair insertion in the F7 gene. Peyvandi, F., Carew, J.A., Perry, D.J., Hunault, M., Khanduri, U., Perkins, S.J., Mannucci, P.M., Bauer, K.A. Blood (2001) [Pubmed]
 
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