Pappalardo Emanuela

Category D - Technical, data processing and scientific-technical Area

Contacts

Workplace

Via Pace, 9 - Ospedale Maggiore Policlinico - Pad. Polo Didattico Vale
20122 MILANO (MI)

Via Pace, 9 - Ospedale Maggiore Policlinico - Fondazione Luigi Villa
20122 MILANO (MI)

Altro numero di telefono
02-55035414
University email address
Research

Publications

Publications
  • The HLA Variant rs6903608 Is Associated with Disease Onset and Relapse of Immune-Mediated Thrombotic Thrombocytopenic Purpura in Caucasians / I. Mancini, E. Giacomini, S. Pontiggia, A. Artoni, B. Ferrari, E. Pappalardo, R. Gualtierotti, S.M. Trisolini, S. Capria, L. Facchini, K. Codeluppi, E. Rinaldi, D. Pastore, S. Campus, C. Caria, A. Caddori, D. Nicolosi, G. Giuffrida, V. Agostini, U. Roncarati, C. Mannarella, A. Fragasso, G.M. Podda, S. Birocchi, A.M. Cerbone, A. Tufano, G. Menna, M. Pizzuti, M. Ronchi, A. De Fanti, S. Amarri, M. Defina, M. Bocchia, S. Cerù, S. Gattillo, F.R. Rosendaal, F. Peyvandi. - In: JOURNAL OF CLINICAL MEDICINE. - ISSN 2077-0383. - 9:10(2020 Oct 21). [Epub ahead of print]
  • Complications of whole-exome sequencing for causal gene discovery in primary platelet secretion defects / M.M. Gorski, A. Lecchi, E.A. Femia, S. La Marca, A. Cairo, E. Pappalardo, L.A. Lotta, A. Artoni, F. Peyvandi. - In: HAEMATOLOGICA. - ISSN 0390-6078. - 104:10(2019 Sep 30), pp. 2084-2090.
  • Next-generation DNA sequencing to identify novel genetic risk factors for cerebral vein thrombosis / M.M. Gorski, H.G. de Haan, I. Mancini, L.A. Lotta, P. Bucciarelli, S.M. Passamonti, A. Cairo, E. Pappalardo, A. van Hylckama Vlieg, I. Martinelli, F.R. Rosendaal, F. Peyvandi. - In: THROMBOSIS RESEARCH. - ISSN 0049-3848. - 169(2018 Sep), pp. 76-81.
  • Platelet to Lymphocyte Ratio and Neutrophil to Lymphocyte Ratio as Risk Factors for Venous Thrombosis / A. Artoni, M. Abbattista, P. Bucciarelli, F. Gianniello, E. Scalambrino, E. Pappalardo, F. Peyvandi, I. Martinelli. - In: CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS. - ISSN 1076-0296. - 24:5(2018 Jul), pp. 808-814.
  • Whole-exome sequencing to identify genetic risk variants underlying inhibitor development in severe hemophilia A patients / M.M. Gorski, K. Blighe, L.A. Lotta, E. Pappalardo, I. Garagiola, I. Mancini, M.E. Mancuso, M.R. Fasulo, E. Santagostino, F. Peyvandi. - In: BLOOD. - ISSN 0006-4971. - 127:23(2016 Jun 09), pp. 2924-2933.