Mechanisms underlying platelet function defect in a pedigree with familial platelet disorder with a predisposition to acute myelogenous leukemia: potential role for candidate RUNX1... by Glembotsky, A. C., Bluteau, D., Espasandin, Y. R., Goette, N. P., Marta, R. F., Marin Oyarzun, C. P., Korin, L., Lev, P. R., Laguens, R. P., Molinas, F. C., Raslova, H., Heller, P. G.

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Anagrelide platelet‐lowering effect is due to inhibition of both megakaryocyte maturation and proplatelet formation: insight into potential mechanisms by Espasandin, Y. R., Glembotsky, A. C., Grodzielski, M., Lev, P. R., Goette, N. P., Molinas, F. C., Marta, R. F., Heller, P. G.

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International collaboration as a tool for diagnosis of patients with inherited thrombocytopenia in the setting of a developing country by GLEMBOTSKY, A. C., MARTA, R. F., PECCI, A., DE ROCCO, D., GNAN, C., ESPASANDIN, Y. R., GOETTE, N. P., NEGRO, F., NORIS, P., SAVOIA, A., BALDUINI, C. L., MOLINAS, F. C., HELLER, P. G.

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Production of functional platelet-like particles by the megakaryoblastic DAMI cell line provides a model for platelet biogenesis by Lev, P. R., Goette, N. P., Glembotsky, A. C., Laguens, R. P., Meckert, P. M. Cabeza, Salim, J. P., Heller, P. G., Pozner, R. G., Marta, R. F., Molinas, F. C.

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Diverse Mpl expression pattern among pedigrees with inherited thrombocytopenia: potential diagnostic and therapeutic implications by HELLER, P. G., GLEMBOTSKY, A. C., GOETTE, N. P., MARTA, R. F., LEV, P. R., MOLINAS, F. C.

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A Deep Dive into the Pathology of Gray Platelet Syndrome: New Insights on Immune Dysregulation by Glembotsky, Ana C, De Luca, Geraldine, Heller, Paula G

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Correlation between platelet phenotype and NBEAL2 genotype in patients with congenital thrombocytopenia and  -granule deficiency by Bottega, R., Pecci, A., De Candia, E., Pujol-Moix, N., Heller, P. G., Noris, P., De Rocco, D., Podda, G. M., Glembotsky, A. C., Cattaneo, M., Balduini, C. L., Savoia, A.

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Low Mpl receptor expression in a pedigree with familial platelet disorder with predisposition to acute myelogenous leukemia and a novel AML1 mutation by Heller, Paula G., Glembotsky, Ana C., Gandhi, Manish J., Cummings, Carrie L., Pirola, Carlos J., Marta, Rosana F., Kornblihtt, Laura I., Drachman, Jonathan G., Molinas, Felisa C.

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The ISTH bleeding assessment tool as predictor of bleeding events in inherited platelet disorders: Communication from the ISTH SSC Subcommittee on Platelet Physiology by Gresele, Paolo, Falcinelli, Emanuela, Bury, Loredana, Pecci, Alessandro, Alessi, Marie‐Christine, Borhany, Munira, Heller, Paula G., Santoro, Cristina, Cid, Ana Rosa, Orsini, Sara, Fontana, Pierre, De Candia, Erica, Podda, Gianmarco, Kannan, Meganathan, Jurk, Kerstin, Castaman, Giancarlo, Falaise, Céline, Guglielmini, Giuseppe, Noris, Patrizia, Zaninetti, Carlo, Fiore, Mathieu, Tosetto, Alberto, Zuniga, Pamela, Miyazaki, Koji, Dupuis, Arnaud, Hayward, Catherine, Casonato, Alessandra, Grandone, Elvira, Mazzucconi, Maria Gabriella, James, Paula, Fabris, Fabrizio, Henskens, Yvonne, Napolitano, Mariasanta, Curnow, Jennifer, Gkalea, Vasiliki, Fedor, Marian, Lambert, Michele P., Zieger, Barbara, Barcella, Luca, Cosmi, Benilde, Giordano, Paola, Porri, Claudia, Melazzini, Federica, Abid, Madiha, Glembotsky, Ana C., Ferrara, Grazia, Russo, Alexandra, Deckmyn, Hans, Frelinger, Andrew L., Harrison, Paul, Mezzano, Diego, Mumford, Andrew D, Lordkipanidzé, Marie

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Platelet Apoptosis in Adult Immune Thrombocytopenia: Insights into the Mechanism of Damage Triggered by Auto-Antibodies by Goette, Nora P, Glembotsky, Ana C, Lev, Paola R, Grodzielski, Matías, Contrufo, Geraldine, Pierdominici, Marta S, Espasandin, Yesica R, Riveros, Dardo, García, Alejandro J, Molinas, Felisa C, Heller, Paula G, Marta, Rosana F

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Downregulation of TREM-like transcript-1 and collagen receptor α2 subunit, two novel RUNX1-targets, contributes to platelet dysfunction in familial platelet disorder with predispos... by Glembotsky, Ana C, Sliwa, Dominika, Bluteau, Dominique, Balayn, Nathalie, Marin Oyarzún, Cecilia P, Raimbault, Anna, Bordas, Marie, Droin, Nathalie, Pirozhkova, Iryna, Washington, Valance, Goette, Nora P, Marta, Rosana F, Favier, Rémi, Raslova, Hana, Heller, Paula G

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Platelet Toll-Like Receptors Mediate Thromboinflammatory Responses in Patients With Essential Thrombocythemia by Marín Oyarzún, Cecilia P, Glembotsky, Ana C, Goette, Nora P, Lev, Paola R, De Luca, Geraldine, Baroni Pietto, María C, Moiraghi, Beatriz, Castro Ríos, Miguel A, Vicente, Angeles, Marta, Rosana F, Schattner, Mirta, Heller, Paula G

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First description of revertant mosaicism in familial platelet disorder with predisposition to acute myelogenous leukemia: correlation with the clinical phenotype by Glembotsky, Ana C, Marin Oyarzún, Cecilia P, De Luca, Geraldine, Marzac, Christophe, Auger, Nathalie, Goette, Nora P, Marta, Rosana F, Raslova, Hana, Heller, Paula G

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Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSC by Gresele, Paolo, Orsini, Sara, Noris, Patrizia, Falcinelli, Emanuela, Alessi, Marie Christine, Bury, Loredana, Borhany, Munira, Santoro, Cristina, Glembotsky, Ana C., Cid, Ana Rosa, Tosetto, Alberto, De Candia, Erica, Fontana, Pierre, Guglielmini, Giuseppe, Pecci, Alessandro, Heller, Paula G., Rodorigo, Giuseppina, Lammle, Bernhard, Trinchero, Alice, Paolo, Radossi, Ferrari, Silvia, Rancitelli, Davide, Stolinski, Amy, Arulselvan, Abinaya, Lassandro, Giuseppe, Luceros, Analia Sanchez, Jandrot‐Perrus, Martine, Kunishima, Shinji, Rivera Pozo, José, Lordkipanidzé, Marie, Melazzini, Federica, Falaise, Céline, Casonato, Alessandra, Podda, Gianmarco, Kannan, Meganathan, Jurk, Kerstin, Sevivas, Teresa, Castaman, Giancarlo, Grandone, Elvira, Fiore, Mathieu, Zuniga, Pamela, Henskens, Yvonne, Miyazaki, Koji, Dupuis, Arnaud, Hayward, Catherine, Zaninetti, Carlo, Abid, Madiha, Ferrara, Grazia, Mazzucconi, Maria Gabriella, Tagariello, Giuseppe, James, Paula, Fabris, Fabrizio, Russo, Alexandra, Bermejo, Nuria, Napolitano, Mariasanta, Curnow, Jennifer, Vasiliki, Gkalea, Zieger, Barbara, Fedor, Marian, Chitlur, Meera, Lambert, Michele, Barcella, Luca, Cosmi, Benilde, Giordano, Paola, Porri, Claudia, Eker, Ibrahim, Morel‐Kopp, Marie‐Christine, Deckmyn, Hans, Frelinger, Andrew L., Harrison, Paul, Mezzano, Diego, Mumford, Andrew D.

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Dysmegakaryopoiesis of FPD/AML pedigrees with constitutional RUNX1 mutations is linked to myosin II deregulated expression by Bluteau, Dominique, Glembotsky, Ana C., Raimbault, Anna, Balayn, Nathalie, Gilles, Laure, Rameau, Philippe, Nurden, Paquita, Alessi, Marie Christine, Debili, Najet, Vainchenker, William, Heller, Paula G., Favier, Remi, Raslova, Hana

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Antithrombotic prophylaxis for surgery-associated venous thromboembolism risk in patients with inherited platelet disorders. The SPATA-DVT Study by Paciullo, Francesco, Bury, Loredana, Noris, Patrizia, Falcinelli, Emanuela, Melazzini, Federica, Orsini, Sara, Zaninetti, Carlo, Abdul-Kadir, Rezan, Obeng-Tuudah, Deborah, Heller, Paula G, Glembotsky, Ana C, Fabris, Fabrizio, Rivera, Jose, Lozano, Maria Luisa, Butta, Nora, Favier, Remi, Cid, Ana Rosa, Fouassier, Marc, Podda, Gian Marco, Santoro, Cristina, Grandone, Elvira, Henskens, Yvonne, Nurden, Paquita, Zieger, Barbara, Cuker, Adam, Devreese, Katrien, Tosetto, Alberto, De Candia, Erica, Dupuis, Arnaud, Miyazaki, Koji, Othman, Maha, Gresele, Paolo

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High cell-free DNA is associated with disease progression, inflammasome activation and elevated levels of inflammasome-related cytokine IL-18 in patients with myelofibrosis by De Luca, Geraldine, Lev, Paola R, Camacho, Maria F, Goette, Nora P, Sackmann, Federico, Castro Ríos, Miguel A, Moiraghi, Beatriz, Cortes Guerrieri, Veronica, Bendek, Georgina, Carricondo, Emiliano, Enrico, Alicia, Vallejo, Veronica, Varela, Ana, Khoury, Marina, Gutierrez, Marina, Larripa, Irene B, Marta, Rosana F, Glembotsky, Ana C, Heller, Paula G

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Pathogenic mechanisms contributing to thrombocytopenia in patients with systemic lupus erythematosus by Baroni Pietto, M. Constanza, Lev, Paola R., Glembotsky, Ana C., Marín Oyarzún, Cecilia P., Gomez, Graciela, Collado, Victoria, Pisoni, Cecilia, Gomez, Ramiro A., Grodzielski, Matías, Gonzalez, Jacqueline, Mariño, Karina V., Heller, Paula G., Goette, Nora P., Marta, Rosana F.

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Neutrophil extracellular trap formation and circulating nucleosomes in patients with chronic myeloproliferative neoplasms by Marin Oyarzún, Cecilia P, Carestia, Agostina, Lev, Paola R, Glembotsky, Ana C, Castro Ríos, Miguel A, Moiraghi, Beatriz, Molinas, Felisa C, Marta, Rosana F, Schattner, Mirta, Heller, Paula G

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Correlation between platelet phenotype and NBEAL2 genotype in patients with congenital thrombocytopenia and α-granule deficiency by 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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