Somatic mutations associated with leukemic progression of familial platelet disorder with predisposition to acute myeloid leukemia
Antony-Debré, I, Duployez, N, Bucci, M, Geffroy, S, Micol, J-B, Renneville, A, Boissel, N, Dhédin, N, Réa, D, Nelken, B, Berthon, C, Leblanc, T, Mozziconacci, M-J, Favier, R, Heller, P G, Abdel-Wahab, O, Raslova, H, Latger-Cannard, V, Preudhomme, C
Published in Leukemia (01.04.2016)
Published in Leukemia (01.04.2016)
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Mechanisms underlying platelet function defect in a pedigree with familial platelet disorder with a predisposition to acute myelogenous leukemia: potential role for candidate RUNX1 targets
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.
Published in Journal of thrombosis and haemostasis (01.05.2014)
Published in Journal of thrombosis and haemostasis (01.05.2014)
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Anagrelide platelet‐lowering effect is due to inhibition of both megakaryocyte maturation and proplatelet formation: insight into potential mechanisms
Espasandin, Y. R., Glembotsky, A. C., Grodzielski, M., Lev, P. R., Goette, N. P., Molinas, F. C., Marta, R. F., Heller, P. G.
Published in Journal of thrombosis and haemostasis (01.04.2015)
Published in Journal of thrombosis and haemostasis (01.04.2015)
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International collaboration as a tool for diagnosis of patients with inherited thrombocytopenia in the setting of a developing country
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.
Published in Journal of thrombosis and haemostasis (01.08.2012)
Published in Journal of thrombosis and haemostasis (01.08.2012)
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Pulmonary hypertension in paroxysmal nocturnal hemoglobinuria
Heller, P G, Grinberg, A R, Lencioni, M, Molina, M M, Roncoroni, A J
Published in Chest (01.08.1992)
Published in Chest (01.08.1992)
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Production of functional platelet-like particles by the megakaryoblastic DAMI cell line provides a model for platelet biogenesis
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.
Published in Platelets (Edinburgh) (01.01.2011)
Published in Platelets (Edinburgh) (01.01.2011)
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Diverse Mpl expression pattern among pedigrees with inherited thrombocytopenia: potential diagnostic and therapeutic implications
HELLER, P. G., GLEMBOTSKY, A. C., GOETTE, N. P., MARTA, R. F., LEV, P. R., MOLINAS, F. C.
Published in Journal of thrombosis and haemostasis (01.12.2008)
Published in Journal of thrombosis and haemostasis (01.12.2008)
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Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia
Noris, Patrizia, Schlegel, Nicole, Klersy, Catherine, Heller, Paula G, Civaschi, Elisa, Pujol-Moix, Nuria, Fabris, Fabrizio, Favier, Remi, Gresele, Paolo, Latger-Cannard, Véronique, Cuker, Adam, Nurden, Paquita, Greinacher, Andreas, Cattaneo, Marco, De Candia, Erica, Pecci, Alessandro, Hurtaud-Roux, Marie-Françoise, Glembotsky, Ana C, Muñiz-Diaz, Eduardo, Randi, Maria Luigia, Trillot, Nathalie, Bury, Loredana, Lecompte, Thomas, Marconi, Caterina, Savoia, Anna, Balduini, Carlo L, Bayart, Sophie, Bauters, Anne, Benabdallah-Guedira, Schéhérazade, Boehlen, Françoise, Borg, Jeanne-Yvonne, Bottega, Roberta, Bussel, James, De Rocco, Daniela, de Maistre, Emmanuel, Faleschini, Michela, Falcinelli, Emanuela, Ferrari, Silvia, Ferster, Alina, Fierro, Tiziana, Fleury, Dominique, Fontana, Pierre, James, Chloé, Lanza, Francois, Le Cam Duchez, Véronique, Loffredo, Giuseppe, Magini, Pamela, Martin-Coignard, Dominique, Menard, Fanny, Mercier, Sandra, Mezzasoma, Annamaria, Minuz, Pietro, Nichele, Ilaria, Notarangelo, Lucia D, Pippucci, Tommaso, Podda, Gian Marco, Pouymayou, Catherine, Rigouzzo, Agnes, Royer, Bruno, Sie, Pierre, Siguret, Virginie, Trichet, Catherine, Tucci, Alessandra, Saposnik, Béatrice, Veneri, Dino
Published in Haematologica (Roma) (01.08.2014)
Published in Haematologica (Roma) (01.08.2014)
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Heavy chain myosin 9-related disease (MYH9 -RD): neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder
Savoia, Anna, De Rocco, Daniela, 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
Published in Thrombosis and haemostasis (01.04.2010)
Published in Thrombosis and haemostasis (01.04.2010)
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Correlation between platelet phenotype and NBEAL2 genotype in patients with congenital thrombocytopenia and -granule deficiency
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.
Published in Haematologica (Roma) (01.06.2013)
Published in Haematologica (Roma) (01.06.2013)
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A Deep Dive into the Pathology of Gray Platelet Syndrome: New Insights on Immune Dysregulation
Glembotsky, Ana C, De Luca, Geraldine, Heller, Paula G
Published in Journal of blood medicine (01.01.2021)
Published in Journal of blood medicine (01.01.2021)
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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
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.
Published in Blood (15.06.2005)
Published in Blood (15.06.2005)
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PDGF‐A, PDGF‐B, TGFβ, and bFGF mRNA levels in patients with essential thrombocythemia treated with anagrelide
Lev, Paola R., Salim, Juan P., Kornblihtt, Laura I., Pirola, Carlos J., Marta, Rosana F., Heller, Paula G., Molinas, Felisa C.
Published in American journal of hematology (01.02.2005)
Published in American journal of hematology (01.02.2005)
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