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Journal Abstract Search

166 related items for PubMed ID: 27283163

  • 21. [Clinical pathological features of the 8p11 myeloproliferative syndrome].
    Yan Z, Yang B, Wang QS, Wang LL, Han XP, Ren F, Yu L.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2010 Oct; 18(5):1321-6. PubMed ID: 21129285
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  • 24. Isodicentric 20q- in two cases of B-cell acute lymphocytic leukemia with the respective t(9;20)(p11;q11.2) and t(9;22)(q34;q11.2).
    Li T, Xue Y, Zhang J, Chen S, Pan J, Wu Y, Wang Y, Shen J.
    Cancer Genet Cytogenet; 2008 Feb; 181(1):55-9. PubMed ID: 18262055
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  • 25. 8p11 myeloproliferative syndrome with t(1;8)(q25;p11.2): a case report and review of the literature.
    Kim WS, Park SG, Park G, Jang SJ, Moon DS, Kang SH.
    Acta Haematol; 2015 Feb; 133(1):101-5. PubMed ID: 25227135
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  • 28. Allogeneic hematopoietic stem cell transplantation for 8p11 myeloproliferative syndrome with BCR-FGFR1 gene rearrangement: a case report and literature review.
    Konishi Y, Kondo T, Nakao K, Asagoe K, Otsuka Y, Nishikori M, Hishizawa M, Yamashita K, Takaori-Kondo A.
    Bone Marrow Transplant; 2019 Feb; 54(2):326-329. PubMed ID: 30087462
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  • 29. [Clinical and laboratory characteristics of two acute lymphoblastic leukemia patients with dicentric (9; 20) (p11 - 13; q11)].
    Gong SL, Qiu HY, Li JY, Han FL, Song XM, Huang ZX, Wang JM.
    Zhonghua Xue Ye Xue Za Zhi; 2006 May; 27(5):306-9. PubMed ID: 16875578
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  • 31. Pemigatinib for the treatment of myeloid/lymphoid neoplasms with FGFR1 rearrangement.
    Freyer CW, Hughes ME, Carulli A, Bagg A, Hexner E.
    Expert Rev Anticancer Ther; 2023 Apr; 23(4):351-359. PubMed ID: 36927350
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  • 33. Leukemic lineage switch in a t(8;22)(p11.2;q11.2)/BCR-FGFR1-rearranged myeloid/lymphoid neoplasm with RUNX1 mutation - diagnostic pitfalls and clinical management including FGFR1 inhibitor pemigatinib.
    Manur R, Sung PJ, Loren AW, Ritchie EK, Frank D, Bagg A, Geyer JT, Bogusz AM.
    Leuk Lymphoma; 2020 Feb; 61(2):450-454. PubMed ID: 31524018
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  • 34. Myeloid/Lymphoid Neoplasm with FGFR1 Rearrangement Presenting with Polycythemia Vera and T-cell Acute Lymphoblastic Leukemia.
    Marinelli LM, Romain JT, Ehman W, Ortega V, Velagaleti G, Gibbons TF, Nazario-Toole A, Holmes AR.
    Cancer Genet; 2023 Aug; 276-277():43-47. PubMed ID: 37480761
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  • 35. Acquisition of genomic events leading to lymphoblastic transformation in a rare case of myeloproliferative neoplasm with BCR-JAK2 fusion transcript.
    Duployez N, Nibourel O, Ducourneau B, Grardel N, Boyer T, Bories C, Darre S, Coiteux V, Berthon C, Preudhomme C, Roche-Lestienne C.
    Eur J Haematol; 2016 Oct; 97(4):399-402. PubMed ID: 26935241
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  • 38. A novel acquired cryptic three-way translocation t(2;11;5)(p21.3;q13.5;q23.2) with a submicroscopic deletion at 11p14.3 in an adult with hypereosinophilic syndrome.
    Kjeldsen E.
    Exp Mol Pathol; 2015 Aug; 99(1):50-5. PubMed ID: 25962659
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  • 40. Mixed phenotype (T/B/myeloid) extramedullary blast crisis as an initial presentation of chronic myelogenous leukemia.
    Qing X, Qing A, Ji P, French SW, Mason H.
    Exp Mol Pathol; 2018 Apr; 104(2):130-133. PubMed ID: 29501750
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