Works matching IS 00071048 AND DT 2012 AND VI 159

Results: 93
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    CBL mutations do not frequently occur in paediatric acute myeloid leukaemia.

    Published in:
    British Journal of Haematology, 2012, v. 159, n. 5, p. 577, doi. 10.1111/bjh.12068
    By:
    • Coenen, Eva A.;
    • Driessen, Emma M. C.;
    • Zwaan, C.Michel;
    • Stary, Jan;
    • Baruchel, Andre;
    • Haas, Valerie;
    • Bont, Eveline S. J. M.;
    • Reinhardt, Dirk;
    • Kaspers, Gertjan J. L.;
    • Arentsen-Peters, Susan T. C. J. M.;
    • Meyer, Claus;
    • Marschalek, Rolf;
    • Pieters, Rob;
    • Stam, Ronald W.;
    • Heuvel-Eibrink, Marry M.
    Publication type:
    Article
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    Common variants within 6p21.31 locus are associated with chronic lymphocytic leukaemia and, potentially, other non- Hodgkin lymphoma subtypes.

    Published in:
    British Journal of Haematology, 2012, v. 159, n. 5, p. 572, doi. 10.1111/bjh.12070
    By:
    • Slager, Susan L.;
    • Camp, Nicola J.;
    • Conde, Lucia;
    • Shanafelt, Tait D.;
    • Achenbach, Sara J.;
    • Rabe, Kari G.;
    • Kay, Neil E.;
    • Novak, Anne J.;
    • Call, Timothy G.;
    • Bracci, Paige M.;
    • Sille, Fenna M. C.;
    • Sanchez, Sylvia;
    • Akers, Nicholas K.;
    • Cunningham, Julie M.;
    • Serie, Daniel J.;
    • McDonnell, Shannon K.;
    • Leis, Jose F.;
    • Wang, Alice H.;
    • Weinberg, J. Brice;
    • Glenn, Martha
    Publication type:
    Article
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    Genetic polymorphisms in ARID5B, CEBPE, IKZF1 and CDKN2A in relation with risk of acute lymphoblastic leukaemia in adults: a Group for Research on Adult Acute Lymphoblastic Leukaemia (GRAALL) study.

    Published in:
    British Journal of Haematology, 2012, v. 159, n. 5, p. 599, doi. 10.1111/bjh.12063
    By:
    • Peyrouze, Pauline;
    • Guihard, Soizic;
    • Grardel, Nathalie;
    • Berthon, Céline;
    • Pottier, Nicolas;
    • Pigneux, Arnaud;
    • Cahn, Jean-Yves;
    • Béné, Marie Christine;
    • Lhéritier, Véronique;
    • Delabesse, Eric;
    • Macintyre, Elizabeth;
    • Thomas, Xavier;
    • Dombret, Hervé;
    • Ifrah, Norbert;
    • Cheok, Meyling
    Publication type:
    Article
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    Lack of negative impact of Philadelphia chromosome in older patients with acute lymphoblastic leukaemia in the thyrosine kinase inhibitor era: comparison of two prospective parallel protocols.

    Published in:
    British Journal of Haematology, 2012, v. 159, n. 4, p. 485, doi. 10.1111/bjh.12043
    By:
    • Ribera, Josep-María;
    • García, Olga;
    • Fernández-Abellán, Pascual;
    • Lavilla, Esperanza;
    • Bernal, María-Teresa;
    • González-Campos, José;
    • Brunet, Salut;
    • Monteserín, María-Carmen;
    • Montesinos, Pau;
    • Sarrá, Josep;
    • Calbacho, Maria;
    • Álvarez-Larrán, Alberto;
    • Tormo, Mar;
    • Oriol, Albert
    Publication type:
    Article
    34

    Author Index.

    Published in:
    British Journal of Haematology, 2012, v. 159, p. 74, doi. 10.1111/j.1365-2141.2012.12071.x
    Publication type:
    Article
    35

    Abstracts.

    Published in:
    2012
    Publication type:
    Abstract
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    Prognostic value of trisomy 8 as a single anomaly and the influence of additional cytogenetic aberrations in primary myelodysplastic syndromes.

    Published in:
    British Journal of Haematology, 2012, v. 159, n. 3, p. 311, doi. 10.1111/bjh.12035
    By:
    • Saumell, Sílvia;
    • Florensa, Lourdes;
    • Luño, Elisa;
    • Sanzo, Carmen;
    • Cañizo, Consuelo;
    • Hernández, Jesus M.;
    • Cervera, José;
    • Gallart, Miguel A.;
    • Carbonell, Félix;
    • Collado, Rosa;
    • Arenillas, Leonor;
    • Pedro, Carme;
    • Bargay, Joan;
    • Nomdedeu, Benet;
    • Xicoy, Blanca;
    • Vallespí, Teresa;
    • Raya, José M.;
    • Belloch, Luis;
    • Sanz, Guillermo F.;
    • Solé, Francesc
    Publication type:
    Article
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    Childhood acute myeloid leukaemia.

    Published in:
    British Journal of Haematology, 2012, v. 159, n. 3, p. 259, doi. 10.1111/bjh.12040
    By:
    • Rubnitz, Jeffrey E.;
    • Inaba, Hiroto
    Publication type:
    Article
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    Magnetic resonance angiography-defined intracranial vasculopathy is associated with silent cerebral infarcts and glucose-6-phosphate dehydrogenase mutation in children with sickle cell anaemia.

    Published in:
    British Journal of Haematology, 2012, v. 159, n. 3, p. 352, doi. 10.1111/bjh.12034
    By:
    • Thangarajh, Mathula;
    • Yang, Genyan;
    • Fuchs, Dana;
    • Ponisio, Maria R.;
    • McKinstry, Robert C.;
    • Jaju, Alok;
    • Noetzel, Michael J.;
    • Casella, James F.;
    • Barron-Casella, Emily;
    • Hooper, W. Craig;
    • Boulet, Sheree L.;
    • Bean, Christopher J.;
    • Pyle, Meredith E.;
    • Payne, Amanda B.;
    • Driggers, Jennifer;
    • Trau, Heidi A.;
    • Vendt, Bruce A.;
    • Rodeghier, Mark;
    • DeBaun, Michael R.
    Publication type:
    Article
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    Erratum.

    Published in:
    2012
    Publication type:
    Erratum
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