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Journal Abstract Search

144 related items for PubMed ID: 9074412

  • 21. Multicolor fluorescence in situ hybridization (SKY) in mycosis fungoides and Sézary syndrome: search for recurrent chromosome abnormalities.
    Batista DA, Vonderheid EC, Hawkins A, Morsberger L, Long P, Murphy KM, Griffin CA.
    Genes Chromosomes Cancer; 2006 Apr; 45(4):383-91. PubMed ID: 16382449
    [Abstract] [Full Text] [Related]

  • 22. Comparison of karyotyping, TCL1 fluorescence in situ hybridisation and TCL1 immunohistochemistry in T cell prolymphocytic leukaemia.
    Sun Y, Tang G, Hu Z, Thakral B, Miranda RN, Medeiros LJ, Wang SA.
    J Clin Pathol; 2018 Apr; 71(4):309-315. PubMed ID: 28821581
    [Abstract] [Full Text] [Related]

  • 23. Recurring structural chromosome abnormalities in peripheral blood lymphocytes of patients with mycosis fungoides/Sézary syndrome.
    Thangavelu M, Finn WG, Yelavarthi KK, Roenigk HH, Samuelson E, Peterson L, Kuzel TM, Rosen ST.
    Blood; 1997 May 01; 89(9):3371-7. PubMed ID: 9129044
    [Abstract] [Full Text] [Related]

  • 24. Aneuploid malignant T cells from a patient with Sézary syndrome can be visualized by in situ hybridization.
    Hindkjaer J, Brandt CA, Kaltoft K.
    Arch Dermatol; 1993 Sep 01; 129(9):1141-5. PubMed ID: 8363397
    [Abstract] [Full Text] [Related]

  • 25. Mature T-cell leukemias including T-prolymphocytic leukemia, adult T-cell leukemia/lymphoma, and Sézary syndrome.
    Foucar K.
    Am J Clin Pathol; 2007 Apr 01; 127(4):496-510. PubMed ID: 17369126
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  • 28. Prognostic significance of cytogenetic abnormalities in T-cell prolymphocytic leukemia.
    Hu Z, Medeiros LJ, Fang L, Sun Y, Tang Z, Tang G, Sun T, Quesada AE, Hu S, Wang SA, Pei L, Lu X.
    Am J Hematol; 2017 May 01; 92(5):441-447. PubMed ID: 28194886
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  • 30. Clinical and laboratory features of 78 cases of T-prolymphocytic leukemia.
    Matutes E, Brito-Babapulle V, Swansbury J, Ellis J, Morilla R, Dearden C, Sempere A, Catovsky D.
    Blood; 1991 Dec 15; 78(12):3269-74. PubMed ID: 1742486
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  • 31. IGH gene involvement in two cases of acute lymphoblastic leukemia with t(14;14)(q11;q32) identified by sequential R-banding and fluorescence in situ hybridization.
    Liu S, Bo L, Liu X, Li C, Qin S, Wang J.
    Cancer Genet Cytogenet; 2004 Jul 15; 152(2):141-5. PubMed ID: 15262434
    [Abstract] [Full Text] [Related]

  • 32. T-cell prolymphocytic leukemia: an aggressive T cell malignancy with frequent cutaneous tropism.
    Magro CM, Morrison CD, Heerema N, Porcu P, Sroa N, Deng AC.
    J Am Acad Dermatol; 2006 Sep 15; 55(3):467-77. PubMed ID: 16908353
    [Abstract] [Full Text] [Related]

  • 33. Chronic lymphocytic leukemia and prolymphocytic leukemia with MYC translocations: a subgroup with an aggressive disease course.
    Put N, Van Roosbroeck K, Konings P, Meeus P, Brusselmans C, Rack K, Gervais C, Nguyen-Khac F, Chapiro E, Radford-Weiss I, Struski S, Dastugue N, Gachard N, Lefebvre C, Barin C, Eclache V, Fert-Ferrer S, Laibe S, Mozziconacci MJ, Quilichini B, Poirel HA, Wlodarska I, Hagemeijer A, Moreau Y, Vandenberghe P, Michaux L, BCGHo and the GFCH.
    Ann Hematol; 2012 Jun 15; 91(6):863-73. PubMed ID: 22205151
    [Abstract] [Full Text] [Related]

  • 34. High levels of chromosomal imbalances in typical and small-cell variants of T-cell prolymphocytic leukemia.
    Costa D, Queralt R, Aymerich M, Carrió A, Rozman M, Vallespí T, Colomer D, Nomdedeu B, Montserrat E, Campo E.
    Cancer Genet Cytogenet; 2003 Nov 15; 147(1):36-43. PubMed ID: 14580769
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  • 35. Burkitt-type acute leukemia in a patient with B-prolymphocytic leukemia: evidence for a common origin.
    Nguyen-Khac F, Davi F, Receveur A, Maloum K, Morel V, Le Garff-Tavernier M, Ong J, Berger R, Leblond V, Merle-Béral H.
    Cancer Genet Cytogenet; 2005 May 15; 159(1):74-8. PubMed ID: 15860362
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  • 36. A complex pattern of recurrent chromosomal losses and gains in T-cell prolymphocytic leukemia.
    Soulier J, Pierron G, Vecchione D, Garand R, Brizard F, Sigaux F, Stern MH, Aurias A.
    Genes Chromosomes Cancer; 2001 Jul 15; 31(3):248-54. PubMed ID: 11391795
    [Abstract] [Full Text] [Related]

  • 37. Combined single nucleotide polymorphism-based genomic mapping and global gene expression profiling identifies novel chromosomal imbalances, mechanisms and candidate genes important in the pathogenesis of T-cell prolymphocytic leukemia with inv(14)(q11q32).
    Dürig J, Bug S, Klein-Hitpass L, Boes T, Jöns T, Martin-Subero JI, Harder L, Baudis M, Dührsen U, Siebert R.
    Leukemia; 2007 Oct 15; 21(10):2153-63. PubMed ID: 17713554
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  • 38. A case of adult T-cell leukaemia/lymphoma characterized by multiplex-fluorescence in situ hybridization, comparative genomic hybridization, fluorescence in situ hybridization and cytogenetics.
    Mao X, Lillington DM, Czepulkowski B, Young BD, Russell-Jones R, Whittaker S.
    Br J Dermatol; 2001 Jul 15; 145(1):117-22. PubMed ID: 11453919
    [Abstract] [Full Text] [Related]

  • 39. The impact of molecular cytogenetics on chronic lymphoid leukaemia.
    Brito-Babapulle V, Garcia-Marco J, Maljaie SH, Hiorns L, Coignet L, Conchon M, Catovsky D.
    Acta Haematol; 1997 Jul 15; 98(4):175-86. PubMed ID: 9401494
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  • 40. Absence of TCR loci chromosomal translocations in cutaneous T-cell lymphomas.
    Salgado R, Gallardo F, Servitje O, Estrach T, García-Muret MP, Romagosa V, Florensa L, Serrano S, Salido M, Solé F, Pujol RM, Espinet B.
    Cancer Genet; 2011 Jul 15; 204(7):405-9. PubMed ID: 21872828
    [Abstract] [Full Text] [Related]

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