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CALR exon 9 mutations are somatically acquired events in familial cases of essential thrombocythemia or primary myelofibrosis
Rumi, Elisa, Harutyunyan, Ashot S., Pietra, Daniela, Milosevic, Jelena D., Casetti, Ilaria C., Bellini, Marta, Them, Nicole C.C., Cavalloni, Chiara, Ferretti, Virginia V., Milanesi, Chiara, Berg, Tiina, Sant'Antonio, Emanuela, Boveri, Emanuela, Pascutto, Cristiana, Astori, Cesare, Kralovics, Robert, Cazzola, Mario
Published in Blood (10.04.2014)
Published in Blood (10.04.2014)
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Essential thrombocythemia in young individuals: frequency and risk factors for vascular events and evolution to myelofibrosis in 126 patients
Alvarez-Larrán, A, Cervantes, F, Bellosillo, B, Giralt, M, Juliá, A, Hernández-Boluda, J C, Bosch, A, Hernández-Nieto, L, Clapés, V, Burgaleta, C, Salvador, C, Arellano-Rodrigo, E, Colomer, D, Besses, C
Published in Leukemia (01.06.2007)
Published in Leukemia (01.06.2007)
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Long term follow up of 93 families with myeloproliferative neoplasms: life expectancy and implications of JAK2V617F in the occurrence of complications
Malak, Sandra, Labopin, Myriam, Saint-Martin, Cecile, Bellanne-Chantelot, Christine, Najman, Albert
Published in Blood cells, molecules, & diseases (15.10.2012)
Published in Blood cells, molecules, & diseases (15.10.2012)
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Acute transformation in nonleukemic chronic myeloproliferative disorders: actuarial probability and main characteristics in a series of 218 patients
Cervantes, F, Tassies, D, Salgado, C, Rovira, M, Pereira, A, Rozman, C
Published in Acta haematologica (01.01.1991)
Published in Acta haematologica (01.01.1991)
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