Spena Silvia

RICERCATORE A TEMPO DETERMINATO (Lettera A)
SSD
MED/03 - GENETICA MEDICA
Settore concorsuale
06/A1 - GENETICA MEDICA

Referenti e contatti

Sede di lavoro

Via Pace, 9 - Fondazione Luigi Villa
20122 MILANO

E-mail di ateneo

Didattica

Ricerca

Pubblicazioni
  • Prediction of Factor VIII inhibitor development in the SIPPET cohort by mutational analysis and Factor VIII antigen measurement / S. Spena, I. Garagiola, A. Cannavò, M. Mortarino, P.M. Mannucci, F.R. Rosendaal, F. Payvandi, A. El-Beshlawy, M. Elalfy, V. Ramanan, P. Eshghi, S. Hanagavadi, R. Varadarajan, M. Karimi, M.V. Manglani, C. Ross, G. Young, T. Seth, S. Apte, D.M. Nayak, E. Santagostino, M.E. Mancuso, A.C. Sandoval Gonzalez, J.N. Mahlangu, S. Bonanad Boix. - In: JOURNAL OF THROMBOSIS AND HAEMOSTASIS. - ISSN 1538-7933. - 16:4(2018 Apr), pp. 778-790.
  • Mutational Repertoire in the SIPPET Cohort and Prediction of FVIII Inhibitor Risk / S. Spena, I. Garagiola, A. Cannavò, M. Mortarino, A. El-Beshlawy, M. Elalfy, V. Ramanan, P. Eshghi, S. Hanagavadi7, R. Varadarajan, M. Karimi, M.V. Manglani, C. Ross, G. Young, T. Seth, S. Apte, D.M. Nayak, E. Santagostino, M.E. Mancuso, A.C. Sandoval Gonzales, J.N. Mahlangu, S. Bonanad, M. Cerqueira, N.P. Ewing, C. Male, T. Owaidah, V. Soto Arellano, N.L. Kobrinsky, S. Majumdar, R. Perez Garrido, A. Sachdeva, M. Simpson, M. Thomas, E. Zanon, B. Antmen, K. Kavakli, M.J. Manco-Johnson, M. Martinez, E. Marzouka, M.G. Mazzucconi, D. Neme, A. Palomo Bravo, R. Paredes Aguilera, A. Prezotti, K. Schmitt, B.M. Wicklund, B. Zulfikar, P.M. Mannucci, F.R. Rosendaal, F. Peyvandi. - In: RESEARCH AND PRACTICE IN THROMBOSIS AND HAEMOSTASIS. - ISSN 2475-0379. - 1:supp. 1(2017), pp. 169-170. ((Intervento presentato al 26. convegno Congress of the International Society on Thrombosis and Haemostasis nel 2017.
  • The Influence of F8 Mutation and Thrombophilic Genetic Markers on Bleeding Phenotype of Patients Affected with Severe Hemophilia A in the SIPPET Cohort / A. Cannavò, S. Spena, R. Palla, I. Garagiola, A. El-Beshlawy, M. Elalfy, V. Ramanan, P. Eshghi, S. Hanagavadi, R. Varadarajan, M. Karimi, M.V. Manglani, C. Ross, G. Young, T. Seth, S. Apte, D.M. Nayak, E. Santagostino, M.E. Mancuso, A.C. Sandoval Gonzales, J.N. Mahlangu, S. Bonanad, M. Cerqueira, N.P. Ewing, C. Male, T. Owaidah, V. Soto Arellano, N.L. Kobrinsky, S. Majumdar, R. Perez Garrido, A. Sachdeva, M. Simpson, M. Thomas, E. Zanon, B. Antmen, K. Kavakli, M.J. Manco-Johnson, M. Martinez, E. Marzouka, M.G. Mazzucconi, D. Neme, A. Palomo, Bravo, R. Paredes Aguilera, A. Prezotti, K. Schmitt, B.M. Wicklund, B. Zulfikar, F.R. Rosendaal, P.M. Mannucci, F. Peyvandi. - In: RESEARCH AND PRACTICE IN THROMBOSIS AND HAEMOSTASIS. - ISSN 2475-0379. - 1:suppl. 1(2017), pp. 797-798. ((Intervento presentato al 26. convegno Congress of the International Society on Thrombosis and Haemostasis nel 2017.
  • Genetic polymorphisms and the development of invasive bacterial infections in children / S. Esposito, S. Bosis, A. Orenti, S. Spena, V. Montinaro, S. Bianchini, A. Zampiero, N. Principi. - In: INTERNATIONAL JOURNAL OF IMMUNOPATHOLOGY AND PHARMACOLOGY. - ISSN 0394-6320. - 29:1(2016 Mar), pp. 99-104.
  • Genetic Polymorphisms of Functional Candidate Genes and Recurrent Acute Otitis Media With or Without Tympanic Membrane Perforation / S. Esposito, P. Marchisio, A. Orenti, S. Spena, S. Bianchini, E. Nazzari, C. Rosazza, A. Zampiero, E. Biganzoli, N. Principi. - In: MEDICINE. - ISSN 0025-7974. - 94:42(2015 Oct).