Search Results - "Molinas, F.C."

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 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.

“…Summary Background Familial platelet disorder with a predisposition to acute myelogenous leukemia (FPD/AML) is an inherited platelet disorder caused by a…”
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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.

“…Summary Background and Objectives Anagrelide represents a treatment option for essential thrombocythemia patients. It lowers platelet counts through inhibition…”
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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.

“…Background:  Inherited thrombocytopenias (ITs) are heterogeneous genetic disorders that frequently represent a diagnostic challenge. The requirement of highly…”
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Monocyte IL-2Rα expression is associated with thrombosis and the JAK2V617F mutation in myeloproliferative neoplasms by Goette, N.P., Lev, P.R., Heller, P.G., Kornblihtt, L.I., Korin, L., Molinas, F.C., Marta, R.F.

“…The development of bone marrow fibrosis and thrombosis are main causes of morbidity in essential thrombocythemia (ET). Monocyte activation has been associated…”
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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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Variation of PDGF, TGFβ, and bFGF levels in essential thrombocythemia patients treated with anagrelide by Lev, P.R., Marta, R.F., Vassallu, P., Molinas, F.C.

“…We studied 15 patients with essential thrombocythemia (ET) before treatment and after normalization of platelet count by anagrelide. Significantly increased…”
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Associated thrombophilic defects in essential thrombocythaemia: their relationship with clinical manifestations by Kornblihtt, L.I, Heller, P.G, Correa, G, Castañón, M, Genoud, V, Vassallu, P, Sarano, J, Kordich, L, Molinas, F.C

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Relationship between hematopoietic growth factors levels and hematological parameters in Argentine hemorrhagic fever by Marta, R.F., Enria, D., Molinas, F.C.

“…Argentine hemorrhagic fever (AHF) is a viral disease caused by Junin virus and characterized by hematologic and neurological involvement. The main hematologic…”
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Systemic disorders in Argentine haemorrhagic fever by Marta, R.F., Montero, V.S., Molinas, F.C.

“…Patients with Argentine haemorrhagic fever have mainly central nervous system involvement and haemorrhagic manifestations, with leucopenia and…”
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Systemic disorders in Argentine haemorrhagic fever by MARTA, R. F, MONTERO, V. S, MOLINAS, F. C

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