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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Journal Article
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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Journal Article
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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Journal Article
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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Journal Article
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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Journal Article
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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Journal Article
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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