PAPPALARDO, EMANUELA
PAPPALARDO, EMANUELA
Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti
Angioedema without urticaria : a large clinical survey
2006 L.C. Zingale, L. Beltrami, A. Zanichelli, L. Maggioni, E. Pappalardo, B. Cicardi, M. Cicardi
Autoantibodies and lymphoproliferative diseases in acquired C1-inhibitor deficiencies
2003 M. Cicardi, L.C. Zingale, E. Pappalardo, A. Folcioni, A. Agostoni
C1 inhibitor : molecular and clinical aspects
2005 M. Cicardi, L. Zingale, A. Zanichelli, E. Pappalardo, B. Cicardi
C1 inhibitor gene expression in patients with hereditary angioedema : quantitative evaluation by means of real-time RT-PCR
2004 E. Pappalardo, L.C. Zingale, M. Cicardi
C1-inhibitor deficiency and angioedema
2001 A. Carugati, E. Pappalardo, L.C. Zingale, M. Cicardi
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
Effect of mutations within the coding region of C1-INH gene on protein function in families with HAE
2005 S. Caccia, E. Pappalardo, L. Maggioni, M. Cicardi
Effects of mutations within the coding region of C1-INH gene on disease manifestation and protein function in families with HAE
2004 S. Caccia, E. Pappalardo, A. Folcioni, L.C. Zingalea, A. Zanichellia, M. Cicardi
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
Frequent de novo mutations and exon deletions in the C1 inhibitor gene of patients with angioedema
2000 E. Pappalardo, M. Cicardi, C. Duponchel, A. Carugati, S. Cloquet, A. Agostoni, M. Tosi
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
Hereditary and acquired angioedema : problems and progress : proceedings of the third C1 esterase inhibitor deficiency workshop and beyond
2004 A. Agostoni, E. Aygoren Pursun, K.E. Binkley, A. Blanch, K. Bork, L. Bouillet, C. Bucher, A.J. Castaldo, M. Cicardi, A.E. Davis, C. De Carolis, C. Drouet, C. Duponchel, H. Farkas, K. Fay, B. Fekete, B. Fischer, L. Fontana, G. Fust, R. Giacomelli, A. Groner, C.E. Hack, G. Harmat, J. Jakenfelds, M. Juers, L. Kalmar, P.N. Kaposi, I. Karadi, A. Kitzinger, T. Kollar, W. Kreuz, P. Lakatos, H.J. Longhurst, M. Lopez Trascasa, I. Martinez Saguer, N. Monnier, I. Nagy, E. Nemeth, E.W. Nielsen, J.H. Nuijens, C. O'Grady, E. Pappalardo, V. Penna, C. Perricone, R. Perricone, U. Rauch, O. Roche, E. Rusicke, P.J. Spath, G. Szendei, E. Takacs, A. Tordai, L. Truedsson, L. Varga, B. Visy, K. Williams, A. Zanichelli, L. Zingale
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
Identification of variables causing different clinical expression of inherited c1-inh deficiency (hereditary angioedema)
2003 E. Pappalardo, S. Caccia, 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
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
Increased expression of C1-inhibitor mRNA in patients with hereditary angioedema treated with Danazol
2003 E. Pappalardo, L.C. Zingale, M. Cicardi
Mechanisms of C1-inhibitor deficiency
2002 E. Pappalardo, L.C. Zingale, A. Terlizzi, A. Zanichelli, A. Folcioni, M. Cicardi
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