Mutations in the 5′ UTR of ANKRD26, the Ankirin Repeat Domain 26 Gene, Cause an Autosomal-Dominant Form of Inherited Thrombocytopenia, THC2 von Pippucci, Tommaso, Savoia, Anna, Perrotta, Silverio, Pujol-Moix, Núria, Noris, Patrizia, Castegnaro, Giovanni, Pecci, Alessandro, Gnan, Chiara, Punzo, Francesca, Marconi, Caterina, Gherardi, Samuele, Loffredo, Giuseppe, De Rocco, Daniela, Scianguetta, Saverio, Barozzi, Serena, Magini, Pamela, Bozzi, Valeria, Dezzani, Luca, Di Stazio, Mariateresa, Ferraro, Marcella, Perini, Giovanni, Seri, Marco, Balduini, Carlo L.

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Position of nonmuscle myosin heavy chain IIA (NMMHC-IIA) mutations predicts the natural history of MYH9-related disease von Pecci, Alessandro, Panza, Emanuele, Pujol-Moix, Núria, Klersy, Catherine, Di Bari, Filomena, Bozzi, Valeria, Gresele, Paolo, Lethagen, Stefan, Fabris, Fabrizio, Dufour, Carlo, Granata, Antonio, Doubek, Michael, Pecoraro, Carmine, Koivisto, Pasi A, Heller, Paula G, Iolascon, Achille, Alvisi, Patrizia, Schwabe, Dirk, De Candia, Erica, Rocca, Bianca, Russo, Umberto, Ramenghi, Ugo, Noris, Patrizia, Seri, Marco, Balduini, Carlo L, Savoia, Anna

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The complex genetic landscape of familial MDS and AML reveals pathogenic germline variants von Rio-Machin, Ana, Vulliamy, Tom, Hug, Nele, Walne, Amanda, Tawana, Kiran, Cardoso, Shirleny, Ellison, Alicia, Pontikos, Nikolas, Wang, Jun, Tummala, Hemanth, Al Seraihi, Ahad Fahad H., Alnajar, Jenna, Bewicke-Copley, Findlay, Armes, Hannah, Barnett, Michael, Bloor, Adrian, Bödör, Csaba, Bowen, David, Fenaux, Pierre, Green, Andrew, Hallahan, Andrew, Hjorth-Hansen, Henrik, Hossain, Upal, Killick, Sally, Lawson, Sarah, Layton, Mark, Male, Alison M., Marsh, Judith, Mehta, Priyanka, Mous, Rogier, Nomdedéu, Josep F., Owen, Carolyn, Pavlu, Jiri, Payne, Elspeth M., Protheroe, Rachel E., Preudhomme, Claude, Pujol-Moix, Nuria, Renneville, Aline, Russell, Nigel, Saggar, Anand, Sciuccati, Gabriela, Taussig, David, Toze, Cynthia L., Uyttebroeck, Anne, Vandenberghe, Peter, Schlegelberger, Brigitte, Ripperger, Tim, Steinemann, Doris, Wu, John, Mason, Joanne, Page, Paula, Akiki, Susanna, Reay, Kim, Cavenagh, Jamie D., Plagnol, Vincent, Caceres, Javier F., Fitzgibbon, Jude, Dokal, Inderjeet

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Genotype–phenotype correlation in MYH9‐related thrombocytopenia von Dong, Fan, Li, Sufeng, Pujol‐Moix, Núria, Luban, Naomi L. C., Shin, Sang Won, Seo, Jae Hong, Ruiz‐Saez, Arlette, Demeter, Judit, Langdon, Scott, Kelley, Michael J.

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Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families von Noris, Patrizia, Perrotta, Silverio, Seri, Marco, Pecci, Alessandro, Gnan, Chiara, Loffredo, Giuseppe, Pujol-Moix, Nuria, Zecca, Marco, Scognamiglio, Francesca, De Rocco, Daniela, Punzo, Francesca, Melazzini, Federica, Scianguetta, Saverio, Casale, Maddalena, Marconi, Caterina, Pippucci, Tommaso, Amendola, Giovanni, Notarangelo, Lucia D., Klersy, Catherine, Civaschi, Elisa, Balduini, Carlo L., Savoia, Anna

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Pseudothrombocytopenia, beyond a laboratory phenomenon: study of 192 cases von Pujol-Moix, Núria, Muñiz-Díaz, Eduardo, Español, Ignacio, Mojal, Sergi, Soler, Alfons, Souto, Juan Carlos

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The scintigraphic index spleen/liver at 30 minutes predicts the success of splenectomy in persistent and chronic primary immune thrombocytopenia von Roca, Manel, Muñiz‐Diaz, Eduardo, Mora, Jaume, Romero‐Zayas, Inmaculada, Ramón, Olga, Roig, Inmaculada, Pujol‐Moix, Núria

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MYH9-Related Disease: A Novel Prognostic Model to Predict the Clinical Evolution of the Disease Based on Genotype-Phenotype Correlations von Pecci, Alessandro, Klersy, Catherine, Gresele, Paolo, Lee, Kieran J.D., De Rocco, Daniela, Bozzi, Valeria, Russo, Giovanna, Heller, Paula G., Loffredo, Giuseppe, Ballmaier, Matthias, Fabris, Fabrizio, Beggiato, Eloise, Kahr, Walter H.A., Pujol-Moix, Nuria, Platokouki, Helen, Van Geet, Christel, Noris, Patrizia, Yerram, Preethi, Hermans, Cedric, Gerber, Bernhard, Economou, Marina, De Groot, Marco, Zieger, Barbara, De Candia, Erica, Fraticelli, Vincenzo, Kersseboom, Rogier, Piccoli, Giorgina B., Zimmermann, Stefanie, Fierro, Tiziana, Glembotsky, Ana C., Vianello, Fabrizio, Zaninetti, Carlo, Nicchia, Elena, Güthner, Christiane, Baronci, Carlo, Seri, Marco, Knight, Peter J., Balduini, Carlo L., Savoia, Anna

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Influence of ABO Locus on PFA-100 Collagen-ADP Closure Time Is Not Totally Dependent on the Von Willebrand Factor. Results of a GWAS on GAIT-2 Project Phenotypes von Pujol-Moix, Núria, Martinez-Perez, Angel, Sabater-Lleal, Maria, Llobet, Dolors, Vilalta, Noèlia, Hamsten, Anders, Souto, Joan Carles, Soria, José Manuel

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Platelet count and plateletcrit are associated with an increased risk of venous thrombosis in females. Results from the RETROVE study von Vázquez-Santiago, Miquel, Vilalta, Noelia, Ziyatdinov, Andrey, Cuevas, Biel, Macho, Raquel, Pujol-Moix, Núria, Carrasco, Marina, Mateo, José, Fontcuberta, Jordi, Soria, José Manuel, Souto, Juan Carlos

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Analysis of 65 pregnancies in 34 women with five different forms of inherited platelet function disorders von Civaschi, Elisa, Klersy, Catherine, Melazzini, Federica, Pujol‐Moix, Nuria, Santoro, Cristina, Cattaneo, Marco, Lavenu‐Bombled, Cécile, Bury, Loredana, Minuz, Pietro, Nurden, Paquita, Cid, Ana R., Cuker, Adam, Latger‐Cannard, Véronique, Favier, Remi, Nichele, Ilaria, Noris, Patrizia

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Short closure time values in PFA–100® are related to venous thrombotic risk. Results from the RETROVE Study von Vázquez-Santiago, Miquel, Vilalta, Noelia, Cuevas, Biel, Murillo, Joaquim, Llobet, Dolors, Macho, Raquel, Pujol-Moix, Núria, Carrasco, Marina, Mateo, José, Fontcuberta, Jordi, Soria, José Manuel, Souto, Juan Carlos

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Correlation between platelet phenotype and NBEAL2 genotype in patients with congenital thrombocytopenia and α-granule deficiency von Bottega, Roberta, Pecci, Alessandro, De Candia, Erica, Pujol-Moix, Nuria, Heller, Paula G, Noris, Patrizia, De Rocco, Daniela, Podda, Gian Marco, Glembotsky, Ana C, Cattaneo, Marco, Balduini, Carlo L, Savoia, Anna

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Heavy chain myosin 9-related disease ( MYH9 -RD): Neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder von Savoia, Anna, Rocco, Daniela De, Panza, Emanuele, Bozzi, Valeria, Scandellari, Raffaella, Loffredo, Giuseppe, Mumford, Andrew, Heller, Paula G., Noris, Patrizia, De Groot, Marco R., Giani, Marisa, Freddi, Paolo, Scognamiglio, Francesca, Riondino, Silvia, Pujol-Moix, Núria, Fabris, Fabrizio, Seri, Marco, Balduini, Carlo L., Pecci, Alessandro

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Genetic determinants of Platelet Large-Cell Ratio, Immature Platelet Fraction, and other platelet-related phenotypes von Pujol-Moix, Núria, Vázquez-Santiago, Miquel, Morera, Agnès, Ziyatdinov, Andrey, Remacha, Angel, Nomdedeu, Josep F, Fontcuberta, Jordi, Soria, José Manuel, Souto, Juan Carlos

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Age and gender effects on 15 platelet phenotypes in a Spanish population von Vázquez-Santiago, Miquel, Ziyatdinov, Andrey, Pujol-Moix, Núria, Brunel, Helena, Morera, Agnès, Soria, José Manuel, Souto, Juan Carlos

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Hydrops fetalis–associated congenital dyserythropoietic anemia treated with intrauterine transfusions and bone marrow transplantation von Remacha, Angel F., Badell, Isabel, Pujol-Moix, Núria, Parra, Juan, Muñiz-Diaz, Eduardo, Ginovart, Gemma, Sardà, M. Pilar, Hernández, Angel, Moliner, Elisenda, Torrent, Montserrat

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Influence of Age, Gender and Lifestyle in Lymphocyte Subsets: Report from the Spanish Gait-2 Study von García-Dabrio, María Concepción, Pujol-Moix, Núria, Martinez-Perez, Ángel, Fontcuberta, Jordi, Souto, Joan Carles, Soria, José Manuel, Nomdedéu, Josep F.

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MYH9 related disease: four novel mutations of the tail domain of myosin-9 correlating with a mild clinical phenotype von Pecci, Alessandro, Panza, Emanuele, De Rocco, Daniela, Pujol-Moix, Nuria, Girotto, Giorgia, Podda, Luigi, Paparo, Carmelo, Bozzi, Valeria, Pastore, Annalisa, Balduini, Carlo L., Seri, Marco, Savoia, Anna

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Assessment of platelet activation in several different anticoagulants by the Advia 120 Hematology System, fluorescence flow cytometry, and electron microscopy von AHNADI, Charaf E, CHAPMAN, E. Sabrinah, LEPINE, Mariette, OKRONGLY, David, PUJOL-MOIX, Nuria, HERNANDEZ, Angel, BOUGHRASSA, Faiza, GRANT, Andrew M

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