Genetic Variants Identified by Whole Exome Sequencing in a Large Italian Family with High Plasma Levels of Factor VIII and Von Willebrand Factor

por Spena, Silvia, Cairo, Andrea, Gianniello, Francesca, Pappalardo, Emanuela, Mortarino, Mimosa, Garagiola, Isabella, Martinelli, Ida, Peyvandi, Flora
Publicado 2023

Platelet to Lymphocyte Ratio and Neutrophil to Lymphocyte Ratio as Risk Factors for Venous Thrombosis

por Artoni, Andrea, Abbattista, Maria, Bucciarelli, Paolo, Gianniello, Francesca, Scalambrino, Erica, Pappalardo, Emanuela, Peyvandi, Flora, Martinelli, Ida
Publicado 2017

Subjective Perception and Psychoacoustic Aspects of the Laryngectomee Voice: The Impact on Quality of Life

por Mesolella, Massimo, Allosso, Salvatore, D’aniello, Roberto, Pappalardo, Emanuela, Catalano, Vincenzo, Quaremba, Giuseppe, Motta, Gaetano, Salerno, Grazia
Publicado 2023

Genetic variants at the chromosomal region 2q21.3 underlying inhibitor development in patients with severe haemophilia A

por Spena, Silvia, Cairo, Andrea, Pappalardo, Emanuela, Gorski, Marcin M., Garagiola, Isabella, Hassan, Shermarke, Gualtierotti, Roberta, Peyvandi, Flora
Publicado 2022

Role of ADAMTS13, VWF and F8 genes in deep vein thrombosis

por Pagliari, Maria Teresa, Cairo, Andrea, Boscarino, Marco, Mancini, Ilaria, Pappalardo, Emanuela, Bucciarelli, Paolo, Martinelli, Ida, Rosendaal, Frits R., Peyvandi, Flora
Publicado 2021

Complications of whole-exome sequencing for causal gene discovery in primary platelet secretion defects

por Gorski, Marcin M., Lecchi, Anna, Femia, Eti A., La Marca, Silvia, Cairo, Andrea, Pappalardo, Emanuela, Lotta, Luca A., Artoni, Andrea, Peyvandi, Flora
Publicado 2019

Single Nucleotide Variant rs2232710 in the Protein Z-Dependent Protease Inhibitor (ZPI, SERPINA10) Gene Is Not Associated with Deep Vein Thrombosis

por Gorski, Marcin M., Lotta, Luca A., Pappalardo, Emanuela, de Haan, Hugoline G., Passamonti, Serena M., van Hylckama Vlieg, Astrid, Martinelli, Ida, Peyvandi, Flora
Publicado 2016

Factor V Leiden but not the factor II 20210G>A mutation is a risk factor for premature coronary artery disease: a case-control study in Iran

por Agosti, Pasquale, Mancini, Ilaria, Sadeghian, Saeed, Pagliari, Maria Teresa, Abbasi, Seyed Hesameddin, Pourhosseini, Hamidreza, Boroumand, Mohammadali, Lotfi-Tokaldany, Masoumeh, Pappalardo, Emanuela, Maino, Alberto, Rosendaal, Frits R., Peyvandi, Flora
Publicado 2023

Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes

por Lotta, Luca A, Wang, Mark, Yu, Jin, Martinelli, Ida, Yu, Fuli, Passamonti, Serena M, Consonni, Dario, Pappalardo, Emanuela, Menegatti, Marzia, Scherer, Steven E, Lewis, Lora L, Akbar, Humeira, Wu, Yuanqing, Bainbridge, Matthew N, Muzny, Donna M, Mannucci, Pier M, Gibbs, Richard A, Peyvandi, Flora
Publicado 2012

The HLA Variant rs6903608 Is Associated with Disease Onset and Relapse of Immune-Mediated Thrombotic Thrombocytopenic Purpura in Caucasians

por Mancini, Ilaria, Giacomini, Elisa, Pontiggia, Silvia, Artoni, Andrea, Ferrari, Barbara, Pappalardo, Emanuela, Gualtierotti, Roberta, Trisolini, Silvia Maria, Capria, Saveria, Facchini, Luca, Codeluppi, Katia, Rinaldi, Erminia, Pastore, Domenico, Campus, Simona, Caria, Cinzia, Caddori, Aldo, Nicolosi, Daniela, Giuffrida, Gaetano, Agostini, Vanessa, Roncarati, Umberto, Mannarella, Clara, Fragasso, Alberto, Podda, Gian Marco, Birocchi, Simone, Cerbone, Anna Maria, Tufano, Antonella, Menna, Giuseppe, Pizzuti, Michele, Ronchi, Michela, De Fanti, Alessandro, Amarri, Sergio, Defina, Marzia, Bocchia, Monica, Cerù, Silvia, Gattillo, Salvatore, Rosendaal, Frits R., Peyvandi, Flora
Publicado 2020

Towards the genetic basis of cerebral venous thrombosis—the BEAST Consortium: a study protocol

por Cotlarciuc, Ioana, Marjot, Thomas, Khan, Muhammad S, Hiltunen, Sini, Haapaniemi, Elena, Metso, Tiina M, Putaala, Jukka, Zuurbier, Susanna M, Brouwer, Matthijs C, Passamonti, Serena M, Bucciarelli, Paolo, Pappalardo, Emanuela, Patel, Tasmin, Costa, Paolo, Colombi, Marina, Canhão, Patrícia, Tkach, Aleksander, Santacroce, Rosa, Margaglione, Maurizio, Favuzzi, Giovanni, Grandone, Elvira, Colaizzo, Donatella, Spengos, Kostas, Arauz, Antonio, Hodge, Amanda, Ditta, Reina, Debette, Stephanie, Zedde, Marialuisa, Pare, Guillaume, Ferro, José M, Thijs, Vincent, Pezzini, Alessandro, Majersik, Jennifer J, Martinelli, Ida, Coutinho, Jonathan M, Tatlisumak, Turgut, Sharma, Pankaj
Publicado 2016

Hereditary and acquired angioedema: Problems and progress: Proceedings of the third C1 esterase inhibitor deficiency workshop and beyond

por Agostoni, Angelo, Aygören-Pürsün, Emel, Binkley, Karen E., Blanch, Alvaro, Bork, Konrad, Bouillet, Laurence, Bucher, Christoph, Castaldo, Anthony J, Cicardi, Marco, Davis, Alvin E, De Carolis, Caterina, Drouet, Christian, Duponchel, Christiane, Farkas, Henriette, Fáy, Kálmán, Fekete, Béla, Fischer, Bettina, Fontana, Luigi, Füst, George, Giacomelli, Roberto, Gröner, Albrecht, Erik Hack, C., Harmat, George, Jakenfelds, John, Juers, Mathias, Kalmár, Lajos, Kaposi, Pál N., Karádi, István, Kitzinger, Arianna, Kollár, Tímea, Kreuz, Wolfhart, Lakatos, Peter, Longhurst, Hilary J., Lopez-Trascasa, Margarita, Martinez-Saguer, Inmaculada, Monnier, Nicole, Nagy, István, Németh, Éva, Nielsen, Erik Waage, Nuijens, Jan H., O'Grady, Caroline, Pappalardo, Emanuela, Penna, Vincenzo, Perricone, Carlo, Perricone, Roberto, Rauch, Ursula, Roche, Olga, Rusicke, Eva, Späth, Peter J, Szendei, George, Takács, Edit, Tordai, Attila, Truedsson, Lennart, Varga, Lilian, Visy, Beáta, Williams, Kayla, Zanichelli, Andrea, Zingale, Lorenza
Publicado 2004