Suchergebnisse - Marta Spreafico

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  1. 1
    Rare bleeding disorders

    Rare bleeding disorders von Flora Peyvandi, Marco Cattaneo, Aida Inbal, Philippe de Moerloose, Marta Spreafico

    Veröffentlicht 2008
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  2. 2
    Clinical and Genomic-Based Decision Support System to Define the Optimal Timing of Allogeneic Hematopoietic Stem-Cell Transplantation in Patients With Myelodysplastic Syndromes

    Clinical and Genomic-Based Decision Support System to Define the Optimal Timing of Allogeneic Hematopoietic Stem-Cell Transplantation in Patients With Myelodysplastic Syndromes von Cristina Astrid Tentori, Caterina Gregorio, Marie Robin, Nico Gagelmann, Carmelo Gurnari, Somedeb Ball, Juan Carlos Caballero Berrocal, Luca Lanino, Saverio D’Amico, Marta Spreafico, Giulia Maggioni, Erica Travaglino, Elisabetta Sauta, Manja Meggendorfer, Lin‐Pierre Zhao, Alessia Campagna, Victor Savevski, Armando Santoro, Najla Al Ali, David A. Sallman, Françesc Solé, Guillermo Garcia‐Manero, Ulrich Germing, Nicolaus Kröger, Shahram Kordasti, Valeria Santini, Guillermo Sanz, Wolfgang Kern, Uwe Platzbecker, María Díez‐Campelo, Jaroslaw P. Maciejewski, Lionel Adès, Pierre Fenaux, Torsten Haferlach, Amer M. Zeidan, Gastone Castellani, Rami S. Komrokji, Francesca Ieva, Matteo Giovanni Della Porta, Massimo Bernardi, Carmen Di Grazia, Luca Vago, Giulia Rivoli, Lorenza Borin, Patrizia Chiusolo, Luisa Giaccone, Maria Teresa Voso, Jan Philipp Bewersdorf, Olivier Nibourel, Marina Díaz Beyà, Andrés Jerez, Francisca Hernández, Kyra Velázquez Kennedy, Blanca Xicoy, Marta Ubezio, Antonio Russo, Gabriele Todisco, Daniele Mannina, Stéfania Bramanti, Matteo Zampini, Elena Riva, Marilena Bicchieri, Gianluca Asti, Filippo Viviani, Alessandro Buizza, Benedetta Tinterri, Anne Sophie Kubasch, Andrea Bacigalupo, Anna Maria Raiola, Alessandro Rambaldi, Francesco Passamonti, Fabio Ciceri

    Veröffentlicht 2024
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  3. 3
    International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways

    International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways von Heather J. Cordell, Younghun Han, George Mells, Yafang Li, Gideon M. Hirschfield, Casey S. Greene, Gang Xie, Brian D. Juran, Dakai Zhu, David C. Qian, James Floyd, Katherine I. Morley, Daniele Prati, Ana Lleó, Daniele Cusi, Erik M. Schlicht, Craig Lammert, Elizabeth J. Atkinson, Landon L. Chan, Mariza de Andrade, Tobias Balschun, Andrew L. Mason, Robert P. Myers, Jinyi Zhang, Piotr Milkiewicz, Jia Qu, Joseph A. Odin, Velimir A. Luketic, Bruce R. Bacon, Henry C. Bodenheimer, Valentina Liakina, Catherine Vincent, Cynthia Levy, Peter K. Gregersen, Piero Luigi Almasio, Domenico Alvaro, Pietro Andreoné, Angelo Andriulli, Cristina Barlassina, Pier Maria Battezzati, A. Benedetti, Francesca Bernuzzi, Ilaria Bianchi, Maria Consiglia Bragazzi, Maurizia Rossana Brunetto, Savino Bruno, Giovanni Casella, B. Coco, Agostino Colli, Massimo Colombo, Sílvia Colombo, Carmela Cursaro, Lory Saveria Crocè, Andrea Crosignani, Maria Francesca Donato, G. Elia, Luca Fabris, Carlo Ferrari, Annarosa Floreani, Barbara Foglieni, Rosanna Fontana, Andrea Galli, Roberta Lazzari, Fabio Salvatore Macaluso, Federica Malinverno, Fabio Marra, Marco Marzioni, Alberto Mattalia, R. Montanari, Lorenzo Morini, Filomena Morisco, Hani S. Mousa, Luigi Muratori, Paolo Muratori, Grazia Anna Niro, Vincenzo Ostilio Palmieri, A. Picciotto, Mauro Podda, Piero Portincasa, Vincenzo Ronca, F. Rosina, Sonia Rossi, Ilaria Sogno, Giancarlo Spinzi, Marta Spreafico, Mario Strazzabosco, Sonia Tarallo, Mirko Tarocchi, Claudio Tiribelli, Pierluigi Toniutto, Maria Cristina Vinci, Massimo Zuin, Chin Lye Ch’ng, Mesbah Rahman, Tom Yapp, Richard Sturgess, Christopher Healey, Marek Czajkowski, Anton Gunasekera, Pranab Gyawali

    Veröffentlicht 2015
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  4. 4
    Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

    Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants von Sekar Kathiresan, Benjamin F. Voight, Shaun Purcell, Kiran Musunuru, Diego Ardissino, Pier M Mannucci, Sonia Anand, James C. Engert, Nilesh J Samani, Heribert Schunkert, Jeanette Erdmann, Muredach P. Reilly, Daniel J. Rader, Thomas Morgan, John A. Spertus, Monika Stoll, Domenico Girelli, Pascal McKeown, Chris C Patterson, David S Siscovick, Christopher J O'Donnell, Roberto Elosúa, Leena Peltonen, Veikko Salomaa, Stephen M Schwartz, Olle Melander, David Altshuler, Pier Angelica Merlini, Carlo Berzuini, Luisa Bernardinelli, Flora Peyvandi, Marco Tubaro, Patrizia Celli, Maurizio Ferrario, Raffaela Fetiveau, Nicola Marziliano, Giorgio Casari, Michele Galli, Flavio Ribichini, Marco Rossi, Francesco Bernardi, Pietro Zonzin, Alberto Piazza, Jean Yee, Yechiel Friedlander, Jaume Marrugat, Gavin Lucas, Isaac Subirana, Joan Sala, Rafel Ramos, James B Meigs, Gordon Williams, David M Nathan, Calum A. MacRae, Aki S Havulinna, Göran Berglund, Joel N. Hirschhorn, Rosanna Asselta, Stefano Duga, Marta Spreafico, Mark Daly, James Nemesh, Joshua M. Korn, Steven A. McCarroll, Aarti Surti, Candace Guiducci, Lauren Gianniny, Daniel B. Mirel, Melissa Parkin, Noël P. Burtt, Stacey B. Gabriel, John R Thompson, Peter S. Braund, Benjamin J. Wright, Anthony J Balmforth, Stephen G. Ball, Alistair S. Hall, Patrick Linsel‐Nitschke, Wolfgang Lieb, Andreas Ziegler, Inke R. König, Christian Hengstenberg, Marcus Fischer, Klaus Stark, Anika Grosshennig, Michael Preuß, H‐Erich Wichmann, Stefan Schreiber, Willem H. Ouwehand, Panos Deloukas, Michael Scholz, Francois Cambien, Mingyao Li, Zhen Chen, Robert Wilensky, William Matthai, Atif Qasim, Hákon Hákonarson, Joe Devaney, Mary-Susan Burnett

    Veröffentlicht 2009
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