PAPPALARDO, EMANUELA
PAPPALARDO, EMANUELA
Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti
Genetic Variants Identified by Whole Exome Sequencing in a Large Italian Family with High Plasma Levels of Factor VIII and Von Willebrand Factor
2023 S. Spena, A. Cairo, F. Gianniello, E. Pappalardo, M. Mortarino, I. Garagiola, I. Martinelli, F. Peyvandi
Genetic variants at the chromosomal region 2q21.3 underlying inhibitor development in patients with severe haemophilia A
2022 S. Spena, A. Cairo, E. Pappalardo, M.M. Gorski, I. Garagiola, S. Hassan, R. Gualtierotti, F. Peyvandi
Role of ADAMTS13, VWF and F8 genes in deep vein thrombosis
2021 M.T. Pagliari, A. Cairo, M. Boscarino, I. Mancini, E. Pappalardo, P. Bucciarelli, I. Martinelli, F.R. Rosendaal, F. Peyvandi
Factor V Leiden but Not Factor II 20210G>A Is a Risk Factor in a Large Cohort of Iranian Patients with Premature Coronary Artery Disease
2020 I. Mancini, S. Sadeghian, M.T. Pagliari, S.H. Abbasi, H. Poorhosseini, M.A. Boroumand, M. Lotfi-Tokaldany, E. Pappalardo, G. Colombo, F. Tafuri, P. Agosti, F.R. Rosendaal, F. Peyvandi
Factor V Leiden but not factor II 20210G>A is a risk factor in a large cohort of Iranian patients with premature coronary artery disease
2020 I. Mancini, S. Sadeghian, M.T. Pagliari, S.H. Abbasi, H. Poorhosseini, M.A. Boroumand, M. Lotfi-tokaldany, E. Pappalardo, G. Colombo, F. Tafuri, P. Agosti, F.R. Rosendaal, F. Peyvandi
The HLA Variant rs6903608 Is Associated with Disease Onset and Relapse of Immune-Mediated Thrombotic Thrombocytopenic Purpura in Caucasians
2020 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
Complications of whole-exome sequencing for causal gene discovery in primary platelet secretion defects
2019 M.M. Gorski, A. Lecchi, E.A. Femia, S. La Marca, A. Cairo, E. Pappalardo, L.A. Lotta, A. Artoni, F. Peyvandi
Next-generation DNA sequencing to identify novel genetic risk factors for cerebral vein thrombosis
2018 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
Platelet to Lymphocyte Ratio and Neutrophil to Lymphocyte Ratio as Risk Factors for Venous Thrombosis
2018 A. Artoni, M. Abbattista, P. Bucciarelli, F. Gianniello, E. Scalambrino, E. Pappalardo, F. Peyvandi, I. Martinelli
Whole-exome sequencing to identify genetic risk variants underlying inhibitor development in severe hemophilia A patients
2016 M.M. Gorski, K. Blighe, L.A. Lotta, E. Pappalardo, I. Garagiola, I. Mancini, M.E. Mancuso, M.R. Fasulo, E. Santagostino, F. Peyvandi
Immunochip analysis identifies novel susceptibility loci in the human leukocyte antigen region for acquired thrombotic thrombocytopenic purpura
2016 I. Mancini, I. Ricano-Ponce, E. Pappalardo, A. Cairo, M.M. Gorski, G. Casoli, B. Ferrari, M. Alberti, D. Mikovic, M. Noris, C. Wijmenga, F. Peyvandi, E. Rinaldi, A. Melpignano, S. Campus, R.A. Podda, C. Caria, A. Caddori, E. Di Francesco, G. Giuffrida, V. Agostini, U. Roncarati, C. Mannarella, A. Fragasso, G.M. Podda, E. Bertinato, A.M. Cerbone, A. Tufano, G. Loffredo, V. Poggi, M. Pizzuti, G. Re, M. Ronchi, K. Codeluppi, L. Facchini, A. De Fanti, S. Amarri, S.M. Trisolini, S. Capria, L. Aprile, M. Defina, S. Ceru
Risk factors for idiopathic sudden sensorineural hearing loss and their association with clinical outcome
2015 S.M. Passamonti, F. Di Berardino, P. Bucciarelli, V. Berto, A. Artoni, F. Gianniello, U. Ambrosetti, A. Cesarani, E. Pappalardo, I. Martinelli
Next-generation sequencing study finds an excess of rare, coding single-nucleotide variants of ADAMTS13 in patients with deep vein thrombosis
2013 L.A. Lotta, G. Tuana, J. Yu, I. Martinelli, M. Wang, F. Yu, S.M. Passamonti, E. Pappalardo, C. Valsecchi, S.E. Scherer, W. Hale, D.M. Muzny, G. Randi, F.R. Rosendaal, R.A. Gibbs, F. Peyvandi
Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes
2012 L.A. LOTTA, M. WANG, J. YU, I. MARTINELLI, F. YU, S.M. PASSAMONTI, D. CONSONNI, E. PAPPALARDO, M. MENEGATTI, S.E. SCHERER, L.L. LEWIS, H. AKBAR, Y. WU, M.N. BAINBRIDGE, D.M. MUZNY, P.M. MANNUCCI, R.A. GIBBS, F. PEYVANDI
Mutation screening of C1 inhibitor gene in 108 unrelated families with hereditary angioedema : functional and structural correlates
2008 E. Pappalardo, S. Caccia, C. Suffritti, A. Tordai, L.C. Zingale, M. Cicardi
Identification of variables causing different clinical expression of inherited c1-inh deficiency (hereditary angioedema)
2007 M. Cicardi, S. Caccia, C. Suffritti, E. Pappalardo, L. Maggioni, L.C. Zingale
Molecular mechanism for the pathogenicity of the human C1-inhibitor Arg378Cys variant
2007 S. Caccia, C. Suffritti, E. Pappalardo, L. Maggioni, L.C. Zingale, M. Cicardi
Structural and functional characterization of mutations in C1-inh responsible for hereditary angioedema
2006 S. Caccia, E. Pappalardo, C. Suffritti, L. Maggioni, A. Zanichelli, L.C. Zingale, B. Cicardi, M. Cicardi
Structural and functional characterization of mutations in C1-ihn responsible for hereditary angioedema
2006 S. Caccia, E. Pappalardo, C. Suffritti, L. Maggioni, A. Zanichelli, L.C. Zingale, B. Cicardi, M. Cicardi
Angioedema without urticaria : a large clinical survey
2006 L.C. Zingale, L. Beltrami, A. Zanichelli, L. Maggioni, E. Pappalardo, B. Cicardi, M. Cicardi