Zobrazuji výsledky 1 - 4 z 4 pro vyhledávání 'Sekeres, M', doba hledání: 0,02 s.
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1
Pathophysiologic and clinical implications of molecular profiles resultant from deletion 5q Autor Adema, V, Palomo, L, Walter, W, Mallo, M, Hutter, S, La Framboise, T, Arenillas, L, Meggendorfer, M, Radivoyevitch, T, Xicoy, B, Pellagatti, A, Haferlach, C, Boultwood, J, Kern, W, Visconte, V, Sekeres, M, Barnard, J, Haferlach, T, Solé, F, Maciejewski, JP
Vydáno 2022Journal article -
2
Recurrent genetic defects on chromosome 5q in myeloid neoplasms Autor Hosono, N, Makishima, H, Mahfouz, R, Przychodzen, B, Yoshida, K, Jerez, A, LaFramboise, T, Polprasert, C, Clemente, M, Shiraishi, Y, Chiba, K, Tanaka, H, Miyano, S, Sanada, M, Cui, E, Verma, A, McDevitt, M, List, A, Saunthararajah, Y, Sekeres, M, Boultwood, J, Ogawa, S, Maciejewski, J
Vydáno 2016Journal article -
3
Loss of heterozygosity in 7q myeloid disorders: clinical associations and genomic pathogenesis. Autor Jerez, A, Sugimoto, Y, Makishima, H, Verma, A, Jankowska, A, Przychodzen, B, Visconte, V, Tiu, R, O'Keefe, C, Mohamedali, A, Kulasekararaj, A, Pellagatti, A, McGraw, K, Muramatsu, H, Moliterno, A, Sekeres, M, McDevitt, M, Kojima, S, List, A, Boultwood, J, Mufti, G, Maciejewski, J
Vydáno 2012Journal article -
4
SF3B1-mutant MDS as a distinct disease subtype: a proposal from the International Working Group for the Prognosis of MDS Autor Malcovati, L, Stevenson, K, Papaemmanuil, E, Neuberg, D, Bejar, R, Boultwood, J, Bowen, DT, Campbell, PJ, Ebert, BL, Fenaux, P, Haferlach, T, Heuser, M, Jansen, JH, Komrokji, RS, Maciejewski, JP, Walter, MJ, Fontenay, M, Garcia-Manero, G, Graubert, TA, Karsan, A, Meggendorfer, M, Pellagatti, A, Sallman, DA, Savona, MR, Sekeres, M, Steensma, DP, Tauro, S, Thol, F, Vyas, P, Van de Loosdrecht, AA, Haase, DT, Tuechler, H, Greenberg, PL, Ogawa, S, Hellstrom-Lindberg, ES, Cazzola, M
Vydáno 2020Journal article