Search Results - "Daraio, Filomena"

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    Monitoring Chronic Myeloid Leukemia: How Molecular Tools May Drive Therapeutic Approaches by Izzo, Barbara, Gottardi, Enrico Marco, Errichiello, Santa, Daraio, Filomena, Baratè, Claudia, Galimberti, Sara

    Published in Frontiers in oncology (06-09-2019)
    “…More than 15 years ago, imatinib entered into the clinical practice as a "magic bullet"; from that point on, the prognosis of patients affected by chronic…”
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    Journal Article
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    Treatment-free remission in Chronic Myeloid Leukemia harboring atypical BCR-ABL1 transcripts by Dragani, Matteo, Petiti, Jessica, Rege-Cambrin, Giovanna, Gottardi, Enrico, Daraio, Filomena, Caocci, Giovanni, Aguzzi, Chiara, Crisà, Elena, Andreani, Giacomo, Caciolli, Francesca, Fava, Carmen

    “…Discontinuation of tyrosine kinase inhibitors (TKI) is the main goal today in the field of Philadelphia positive chronic myeloid leukemia (Ph + CML) and the…”
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    Genetic and clinical heterogeneity of ferroportin disease by Cemonesi, Laura, Forni, Gian Luca, Soriani, Nadia, Lamagna, Martina, Fermo, Isabella, Daraio, Filomena, Galli, Anna, Pietra, Daniela, Malcovati, Luca, Ferrari, Maurizio, Camaschella, Clara, Cazzola, Mario

    Published in British journal of haematology (01-12-2005)
    “…Summary Ferroportin is encoded by the SLC40A1 gene and mediates iron export from cells by interacting with hepcidin. SLC40A1 gene mutations are associated with…”
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    Philadelphia-positive lymphoblastic lymphoma: a case report and review of the literature by Dragani, Matteo, Andreani, Giacomo, Fava, Carmen, Daraio, Filomena, Gottardi, Enrico, Giugliano, Emilia, Nicoli, Paolo, Rege-Cambrin, Giovanna

    Published in Stem cell investigation (2019)
    “…Philadelphia positive acute lymphoblastic leukemia is well documented nowadays but very little is known about Philadelphia positive lymphoblastic lymphoma…”
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    Spectrum of hemojuvelin gene mutations in 1q-linked juvenile hemochromatosis by Lanzara, Carmela, Roetto, Antonella, Daraio, Filomena, Rivard, Silvain, Ficarella, Romina, Simard, Hervey, Cox, Timothy M., Cazzola, Mario, Piperno, Alberto, Gimenez-Roqueplo, Anne-Paule, Grammatico, Paola, Volinia, Stefano, Gasparini, Paolo, Camaschella, Clara

    Published in Blood (01-06-2004)
    “…Juvenile or type 2 hemochromatosis (JH) is transmitted as a recessive trait that leads to severe iron overload and organ damage typically before age 30 years…”
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    Clinical and pathologic findings in hemochromatosis type 3 due to a novel mutation in transferrin receptor 2 gene by Girelli, Domenico, Bozzini, Claudia, Roetto, Antonella, Alberti, Federica, Daraio, Filomena, Colombari, Romano, Olivieri, Oliviero, Corrocher, Roberto, Camaschella, Clara

    Published in Gastroenterology (New York, N.Y. 1943) (01-05-2002)
    “…Although most patients with hereditary hemochromatosis are homozygous for a single mutation of the HFE gene on chromosome 6p, accumulating evidence indicates…”
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