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947 related items for PubMed ID: 17574959

  • 1. Fluorescence in situ hybridization analysis of 110 hematopoietic disorders with chromosome 5 abnormalities: do de novo and therapy-related myelodysplastic syndrome-acute myeloid leukemia actually differ?
    Lessard M, Hélias C, Struski S, Perrusson N, Uettwiller F, Mozziconacci MJ, Lafage-Pochitaloff M, Dastugue N, Terré C, Brizard F, Cornillet-Lefebvre P, Mugneret F, Barin C, Herry A, Luquet I, Desangles F, Michaux L, Verellen-Dumoulin C, Perrot C, Van den Akker J, Lespinasse J, Eclache V, Berger R, Groupe Francophone de Cytogénétique Hématologique.
    Cancer Genet Cytogenet; 2007 Jul 01; 176(1):1-21. PubMed ID: 17574959
    [Abstract] [Full Text] [Related]

  • 2. Multiplex fluorescence in situ hybridization in identifying chromosome involvement of complex karyotypes in de novo myelodysplastic syndromes and acute myeloid leukemia.
    Xu W, Li JY, Liu Q, Zhu Y, Pan JL, Qiu HR, Xue YQ.
    Int J Lab Hematol; 2010 Feb 01; 32(1 Pt 1):e86-95. PubMed ID: 20089000
    [Abstract] [Full Text] [Related]

  • 3. Evaluation of chromosome 5 aberrations in complex karyotypes of patients with myeloid disorders reveals their contribution to dicentric and tricentric chromosomes, resulting in the loss of critical 5q regions.
    Herry A, Douet-Guilbert N, Morel F, Le Bris MJ, Morice P, Abgrall JF, Berthou C, De Braekeleer M.
    Cancer Genet Cytogenet; 2007 Jun 01; 175(2):125-31. PubMed ID: 17556068
    [Abstract] [Full Text] [Related]

  • 4. Redefining monosomy 5 by molecular cytogenetics in 23 patients with MDS/AML.
    Herry A, Douet-Guilbert N, Morel F, Le Bris MJ, De Braekeleer M.
    Eur J Haematol; 2007 Jun 01; 78(6):457-67. PubMed ID: 17391336
    [Abstract] [Full Text] [Related]

  • 5. Role of multiplex FISH in identifying chromosome involvement in myelodysplastic syndromes and acute myeloid leukemias with complex karyotypes: a report on 28 cases.
    Barouk-Simonet E, Soenen-Cornu V, Roumier C, Cosson A, Laï JL, Fenaux P, Preudhomme C.
    Cancer Genet Cytogenet; 2005 Mar 01; 157(2):118-26. PubMed ID: 15721632
    [Abstract] [Full Text] [Related]

  • 6. Fluorescence in situ hybridization improves the detection of 5q31 deletion in myelodysplastic syndromes without cytogenetic evidence of 5q-.
    Mallo M, Arenillas L, Espinet B, Salido M, Hernández JM, Lumbreras E, del Rey M, Arranz E, Ramiro S, Font P, González O, Renedo M, Cervera J, Such E, Sanz GF, Luño E, Sanzo C, González M, Calasanz MJ, Mayans J, García-Ballesteros C, Amigo V, Collado R, Oliver I, Carbonell F, Bureo E, Insunza A, Yañez L, Muruzabal MJ, Gómez-Beltrán E, Andreu R, León P, Gómez V, Sanz A, Casasola N, Moreno E, Alegre A, Martín ML, Pedro C, Serrano S, Florensa L, Solé F.
    Haematologica; 2008 Jul 01; 93(7):1001-8. PubMed ID: 18591625
    [Abstract] [Full Text] [Related]

  • 7. Submicroscopic deletions in 5q- associated malignancies.
    Crescenzi B, La Starza R, Romoli S, Beacci D, Matteucci C, Barba G, Aventin A, Marynen P, Ciolli S, Nozzoli C, Martelli MF, Mecucci C.
    Haematologica; 2004 Mar 01; 89(3):281-5. PubMed ID: 15020265
    [Abstract] [Full Text] [Related]

  • 8. Structural aberrations of chromosome 7 revealed by a combination of molecular cytogenetic techniques in myeloid malignancies.
    Brezinová J, Zemanová Z, Ransdorfová S, Pavlistová L, Babická L, Housková L, Melichercíková J, Sisková M, Cermák J, Michalová K.
    Cancer Genet Cytogenet; 2007 Feb 01; 173(1):10-6. PubMed ID: 17284364
    [Abstract] [Full Text] [Related]

  • 9. [Abnormalities of chromosome 17 in myeloid malignancies with complex chromosomal abnormalities].
    Zhu Y, Xu W, Liu Q, Pan J, Qiu H, Wang R, Qiao C, Jiang Y, Zhang S, Fan L, Zhang J, Shen Y, Xue Y, Li J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct 01; 25(5):579-82. PubMed ID: 18841577
    [Abstract] [Full Text] [Related]

  • 10. Cytogenetic features of 5q deletion and 5q- syndrome in myelodysplastic syndrome in Korea; marker chromosomes proved to be chromosome 5 with interstitial deletion by fluorescence in situ hybridization.
    Lee HR, Oh B, Hong DS, Zang DY, Yoon HJ, Kim HJ, Kim I, Ahn JS, Cheong JW, Lee KA, Cho KS, Lee MH, Bang SM, Kim TY, Yun YM, Min YH, Lee YK, Lee DS, AML/MDS Working Party of the Korean Society of Hematology.
    Cancer Genet Cytogenet; 2010 Dec 01; 203(2):193-202. PubMed ID: 21156233
    [Abstract] [Full Text] [Related]

  • 11. Loss of genetic material is more common than gain in acute myeloid leukemia with complex aberrant karyotype: a detailed analysis of 125 cases using conventional chromosome analysis and fluorescence in situ hybridization including 24-color FISH.
    Schoch C, Haferlach T, Bursch S, Gerstner D, Schnittger S, Dugas M, Kern W, Löffler H, Hiddemann W.
    Genes Chromosomes Cancer; 2002 Sep 01; 35(1):20-9. PubMed ID: 12203786
    [Abstract] [Full Text] [Related]

  • 12. Molecular cytogenetic profiling of complex karyotypes in primary myelodysplastic syndromes and acute myeloid leukemia.
    Trost D, Hildebrandt B, Beier M, Müller N, Germing U, Royer-Pokora B.
    Cancer Genet Cytogenet; 2006 Feb 01; 165(1):51-63. PubMed ID: 16490597
    [Abstract] [Full Text] [Related]

  • 13. Pooled analysis of clinical and cytogenetic features in treatment-related and de novo adult acute myeloid leukemia and myelodysplastic syndromes based on a consecutive series of 761 patients analyzed 1976-1993 and on 5098 unselected cases reported in the literature 1974-2001.
    Mauritzson N, Albin M, Rylander L, Billström R, Ahlgren T, Mikoczy Z, Björk J, Strömberg U, Nilsson PG, Mitelman F, Hagmar L, Johansson B.
    Leukemia; 2002 Dec 01; 16(12):2366-78. PubMed ID: 12454741
    [Abstract] [Full Text] [Related]

  • 14. Conventional and molecular cytogenetic features of myelodysplastic syndrome in China.
    Chen L, Li J, Zhu Y, Qiu H, Pan J, Wang R, Qian S, Xu W, Xue Y.
    Exp Oncol; 2007 Dec 01; 29(4):299-303. PubMed ID: 18199987
    [Abstract] [Full Text] [Related]

  • 15. [Detection of cytogenetic abnormalities involving chromosomes 5,7 and 8 in myelodysplastic syndromes with fluorescence in situ hybridization and its clinical significance].
    Cai Y, Qin YW, Wang C, Yang J, Yan SK.
    Zhonghua Xue Ye Xue Za Zhi; 2007 Jan 01; 28(1):6-10. PubMed ID: 17649717
    [Abstract] [Full Text] [Related]

  • 16. Incidence and significance of cryptic chromosome aberrations detected by fluorescence in situ hybridization in acute myeloid leukemia with normal karyotype.
    Cuneo A, Bigoni R, Cavazzini F, Bardi A, Roberti MG, Agostini P, Tammiso E, Ciccone N, Mancini M, Nanni M, De Cuia R, Divona M, La Starza R, Crescenzi B, Testoni N, Rege Cambrin G, Mecucci C, Lo Coco F, Saglio G, Castoldi G.
    Leukemia; 2002 Sep 01; 16(9):1745-51. PubMed ID: 12200689
    [Abstract] [Full Text] [Related]

  • 17. Chromosomal aberrations in bone marrow mesenchymal stroma cells from patients with myelodysplastic syndrome and acute myeloblastic leukemia.
    Blau O, Hofmann WK, Baldus CD, Thiel G, Serbent V, Schümann E, Thiel E, Blau IW.
    Exp Hematol; 2007 Feb 01; 35(2):221-9. PubMed ID: 17258071
    [Abstract] [Full Text] [Related]

  • 18. [Detection of common chromosome abnormalities in myelodysplastic syndrome with a panel fluorescence in situ hybridization].
    Shen Y, Xue Y, Li J, Pan J, Wu Y, Chen S.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Apr 01; 20(2):160-3. PubMed ID: 12673589
    [Abstract] [Full Text] [Related]

  • 19. Cytogenetic abnormalities in 532 patients with myeloid leukemias and myelodyplastic syndrome. The Czechoslovak MDS Cooperative Group.
    Michalová K, Musilová J, Zemanová Z.
    Czech Med; 1990 Apr 01; 13(4):133-44. PubMed ID: 2081440
    [Abstract] [Full Text] [Related]

  • 20. Conventional and molecular cytogenetic findings of myelodysplastic syndrome patients.
    Yilmaz Z, Sahin FI, Kizilkilic E, Karakus S, Boga C, Ozdogu H.
    Clin Exp Med; 2005 Jul 01; 5(2):55-9. PubMed ID: 16096854
    [Abstract] [Full Text] [Related]

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