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Journal Abstract Search

250 related items for PubMed ID: 32624544

  • 1. [Familial leukemia due to germline RUNX1 mutations: lessons learned from two decades of research and unsolved problems].
    Osato M, Nambu A.
    Rinsho Ketsueki; 2020; 61(6):687-696. PubMed ID: 32624544
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  • 2. [A new form of familial platelet disorder caused by germline mutations in RUNX1 in a pedigree].
    Guan J, Wang LL, Wang CY, Zhu XM, Shuai HZ, Yi X, Zou L, Yu D, Cheng H.
    Zhonghua Nei Ke Za Zhi; 2023 Apr 01; 62(4):393-400. PubMed ID: 37032134
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  • 3. Unrelated hematopoietic stem cell transplantation for familial platelet disorder/acute myeloid leukemia with germline RUNX1 mutations.
    Toratani K, Watanabe M, Kanda J, Oka T, Hyuga M, Arai Y, Iwasaki M, Sakurada M, Nannya Y, Ogawa S, Yamada T, Takaori-Kondo A.
    Int J Hematol; 2023 Sep 01; 118(3):400-405. PubMed ID: 36897502
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  • 7. [Familial platelet disorder with predisposition to myeloid leukemia (FPD/AML): a case report and literature review].
    Zhang RR, Chen XJ, Ren YY, Yang WY, Zhu XF.
    Zhonghua Xue Ye Xue Za Zhi; 2021 Apr 14; 42(4):308-312. PubMed ID: 33979975
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  • 11. RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML.
    Brown AL, Arts P, Carmichael CL, Babic M, Dobbins J, Chong CE, Schreiber AW, Feng J, Phillips K, Wang PPS, Ha T, Homan CC, King-Smith SL, Rawlings L, Vakulin C, Dubowsky A, Burdett J, Moore S, McKavanagh G, Henry D, Wells A, Mercorella B, Nicola M, Suttle J, Wilkins E, Li XC, Michaud J, Brautigan P, Cannon P, Altree M, Jaensch L, Fine M, Butcher C, D'Andrea RJ, Lewis ID, Hiwase DK, Papaemmanuil E, Horwitz MS, Natsoulis G, Rienhoff HY, Patton N, Mapp S, Susman R, Morgan S, Cooney J, Currie M, Popat U, Bochtler T, Izraeli S, Bradstock K, Godley LA, Krämer A, Fröhling S, Wei AH, Forsyth C, Mar Fan H, Poplawski NK, Hahn CN, Scott HS.
    Blood Adv; 2020 Mar 24; 4(6):1131-1144. PubMed ID: 32208489
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  • 12. High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorder.
    Preudhomme C, Renneville A, Bourdon V, Philippe N, Roche-Lestienne C, Boissel N, Dhedin N, André JM, Cornillet-Lefebvre P, Baruchel A, Mozziconacci MJ, Sobol H.
    Blood; 2009 May 28; 113(22):5583-7. PubMed ID: 19357396
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  • 14. CBL mutation in chronic myelomonocytic leukemia secondary to familial platelet disorder with propensity to develop acute myeloid leukemia (FPD/AML).
    Shiba N, Hasegawa D, Park MJ, Murata C, Sato-Otsubo A, Ogawa C, Manabe A, Arakawa H, Ogawa S, Hayashi Y.
    Blood; 2012 Mar 15; 119(11):2612-4. PubMed ID: 22138511
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