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Silvia G. Priori

Department of Molecular Cardiology

Fondazione Salvatore Maugeri

Pavia

Italy

[email]@fsm.it

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Molecular Cardiology, Fondazione Salvatore Maugeri, Pavia, Italy. 2000 - 2009
  • Molecular Cardiology and Electrophysiology Laboratory, Fondazione S. Maugeri, IRCCS, Pavia, Italy. 1999 - 2006
  • Molecular Cardiology, Maugeri Foundation, Pavia, Italy. 2003 - 2006
  • European Society of Cardilogy, Alice, France. 2004
  • Molecular Cardiology, IRCCS Salvatore Maugeri Foundation, and University of Pavia, Italy. 2004
  • Department of Molecular Cardiology, Istituto di Ricovero e Cura a Carattere Scientifico Fondazione S. Maugeri, University of Pavia, Pavia, Italy. 2003
  • Task Force on Sudden Cardiac Death of the European Society of Cardiology, Fondazione Salvatore Maugeri, University of Pavia, Italy. 2002

References

  1. To replace or not to replace: a systematic approach to respond to device advisories. Priori, S.G., Auricchio, A., Nisam, S., Yong, P. J. Cardiovasc. Electrophysiol. (2009) [Pubmed]
  2. Role of genetic analyses in cardiology: part I: mendelian diseases: cardiac channelopathies. Priori, S.G., Napolitano, C. Circulation (2006) [Pubmed]
  3. Experimental therapy of genetic arrhythmias: disease-specific pharmacology. Priori, S.G., Napolitano, C., Cerrone, M. Handb. Exp. Pharmacol (2006) [Pubmed]
  4. A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene. Priori, S.G., Pandit, S.V., Rivolta, I., Berenfeld, O., Ronchetti, E., Dhamoon, A., Napolitano, C., Anumonwo, J., di Barletta, M.R., Gudapakkam, S., Bosi, G., Stramba-Badiale, M., Jalife, J. Circ. Res. (2005) [Pubmed]
  5. Genetic arrhythmias. Priori, S.G., Cerrone, M. Ital. Heart. J (2005) [Pubmed]
  6. Cardiac and skeletal muscle disorders caused by mutations in the intracellular Ca2+ release channels. Priori, S.G., Napolitano, C. J. Clin. Invest. (2005) [Pubmed]
  7. Inherited arrhythmogenic diseases: the complexity beyond monogenic disorders. Priori, S.G. Circ. Res. (2004) [Pubmed]
  8. ESC-ERC recommendations for the use of automated external defibrillators (AEDs) in Europe. Priori, S.G., Bossaert, L.L., Chamberlain, D.A., Napolitano, C., Arntz, H.R., Koster, R.W., Monsieurs, K.G., Capucci, A., Wellens, H.J. Eur. Heart J. (2004) [Pubmed]
  9. Policy statement: ESC-ERC recommendations for the use of automated external defibrillators (AEDs) in Europe. Priori, S.G., Bossaert, L.L., Chamberlain, D.A., Napolitano, C., Arntz, H.R., Koster, R.W., Monsieurs, K.G., Capucci, A., Wellens, H.H. Resuscitation (2004) [Pubmed]
  10. Genetics of cardiac arrhythmias and sudden cardiac death. Priori, S.G., Napolitano, C. Ann. N. Y. Acad. Sci. (2004) [Pubmed]
  11. Association of long QT syndrome loci and cardiac events among patients treated with beta-blockers. Priori, S.G., Napolitano, C., Schwartz, P.J., Grillo, M., Bloise, R., Ronchetti, E., Moncalvo, C., Tulipani, C., Veia, A., Bottelli, G., Nastoli, J. JAMA (2004) [Pubmed]
  12. Risk stratification in the long-QT syndrome. Priori, S.G., Schwartz, P.J., Napolitano, C., Bloise, R., Ronchetti, E., Grillo, M., Vicentini, A., Spazzolini, C., Nastoli, J., Bottelli, G., Folli, R., Cappelletti, D. N. Engl. J. Med. (2003) [Pubmed]
  13. Inherited arrhythmia syndromes: applying the molecular biology and genetic to the clinical management. Priori, S.G., Napolitano, C., Vicentini, A. J. Interv. Card. Electrophysiol (2003) [Pubmed]
  14. Medical Practice Guidelines. Separating science from economics. Priori, S.G., Klein, W., Bassand, J.P. Eur. Heart J. (2003) [Pubmed]
  15. Task Force on Sudden Cardiac Death, European Society of Cardiology. Priori, S.G., Aliot, E., Blømstrom-Lundqvist, C., Bossaert, L., Breithardt, G., Brugada, P., Camm, J.A., Cappato, R., Cobbe, S.M., Di, M.C., Maron, B.J., McKenna, W.J., Pedersen, A.K., Ravens, U., Schwartz, P.J., Trusz-Gluza, M., Vardas, P., Wellens, H.J., Zipes, D.P. Europace (2002) [Pubmed]
  16. Natural history of Brugada syndrome: insights for risk stratification and management. Priori, S.G., Napolitano, C., Gasparini, M., Pappone, C., Della Bella, P., Giordano, U., Bloise, R., Giustetto, C., De Nardis, R., Grillo, M., Ronchetti, E., Faggiano, G., Nastoli, J. Circulation (2002) [Pubmed]
  17. Genetic defects of cardiac ion channels. The hidden substrate for torsades de pointes. Priori, S.G., Napolitano, C. Cardiovasc. Drugs. Ther (2002) [Pubmed]
  18. Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia. Priori, S.G., Napolitano, C., Memmi, M., Colombi, B., Drago, F., Gasparini, M., DeSimone, L., Coltorti, F., Bloise, R., Keegan, R., Cruz Filho, F.E., Vignati, G., Benatar, A., DeLogu, A. Circulation (2002) [Pubmed]
  19. Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia. Priori, S.G., Napolitano, C., Tiso, N., Memmi, M., Vignati, G., Bloise, R., Sorrentino, V., Danieli, G.A. Circulation (2001) [Pubmed]
  20. The long QT syndrome. Priori, S.G., Bloise, R., Crotti, L. Europace (2001) [Pubmed]
  21. Concealed arrhythmogenic syndromes: the hidden substrate of idiopathic ventricular fibrillation?. Priori, S.G., Napolitano, C., Grillo, M. Cardiovasc. Res. (2001) [Pubmed]
  22. The elusive link between LQT3 and Brugada syndrome: the role of flecainide challenge. Priori, S.G., Napolitano, C., Schwartz, P.J., Bloise, R., Crotti, L., Ronchetti, E. Circulation (2000) [Pubmed]
  23. Gene specific therapy for arrhythmogenic disorders. Priori, S.G., Ronchetti, E., Memmi, M. Ital. Heart. J (2000) [Pubmed]
  24. Long QT and Brugada syndromes: from genetics to clinical management. Priori, S.G. J. Cardiovasc. Electrophysiol. (2000) [Pubmed]
  25. Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: A prospective evaluation of 52 families. Priori, S.G., Napolitano, C., Gasparini, M., Pappone, C., Della Bella, P., Brignole, M., Giordano, U., Giovannini, T., Menozzi, C., Bloise, R., Crotti, L., Terreni, L., Schwartz, P.J. Circulation (2000) [Pubmed]
  26. Genetic and molecular basis of cardiac arrhythmias: impact on clinical management parts I and II. Priori, S.G., Barhanin, J., Hauer, R.N., Haverkamp, W., Jongsma, H.J., Kleber, A.G., McKenna, W.J., Roden, D.M., Rudy, Y., Schwartz, K., Schwartz, P.J., Towbin, J.A., Wilde, A.M. Circulation (1999) [Pubmed]
  27. Low penetrance in the long-QT syndrome: clinical impact. Priori, S.G., Napolitano, C., Schwartz, P.J. Circulation (1999) [Pubmed]
  28. Genetic and molecular basis of cardiac arrhythmias: impact on clinical management part III. Priori, S.G., Barhanin, J., Hauer, R.N., Haverkamp, W., Jongsma, H.J., Kleber, A.G., McKenna, W.J., Roden, D.M., Rudy, Y., Schwartz, K., Schwartz, P.J., Towbin, J.A., Wilde, A.M. Circulation (1999) [Pubmed]
 
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