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	Amedeo Prize 2008 The 21 Finalists

Leukemia

Free Subscription Articles published in Cancer Genet Cytogenet Retrieve available abstracts of 128 articles: HTML format

Single Articles

April 2008
1. RAMKUMAR B , Chadha MK, Barcos M, Sait SN, et al
   Acute promyelocytic leukemia after mitoxantrone therapy for multiple sclerosis.
   Cancer Genet Cytogenet. 2008;182:126-9.
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2. DE MELO VA , Milojkovic D, Marin D, Apperley JF, et al
   Deletions adjacent to BCR and ABL1 breakpoints occur in a substantial minority of chronic myeloid leukemia patients with masked Philadelphia rearrangements.
   Cancer Genet Cytogenet. 2008;182:111-5.
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3. RICHEBOURG S , Eclache V, Perot C, Portnoi MF, et al
   Mechanisms of genesis of variant translocation in chronic myeloid leukemia are not correlated with ABL1 or BCR deletion status or response to imatinib therapy.
   Cancer Genet Cytogenet. 2008;182:95-102.
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4. WANG HP , Chen ZM, Lou JY, Xu H, et al
   Additional rearrangements affecting the derivative chromosome 9 involved in the standard Philadelphia translocation after imatinib therapy in a patient with chronic myeloid leukemia.
   Cancer Genet Cytogenet. 2008;182:63-4.
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5. MACEDO SILVA ML , Raimondi SC, Abdelhay E, Gross M, et al
   Banding and molecular cytogenetic studies detected a CBFB-MYH11 fusion gene that appeared as abnormal chromosomes 1 and 16 in a baby with acute myeloid leukemia FAB M4-Eo.
   Cancer Genet Cytogenet. 2008;182:56-60.
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6. STAVROPOULOU C , Georgakakos VN, Manola KN, Pagoni M, et al
   5'RARA submicroscopic deletion from new variant translocation involving chromosomes 15, 17, and 18, in a case of acute promyelocytic leukemia.
   Cancer Genet Cytogenet. 2008;182:50-5.
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7. PIDALA J , Pinilla-Ibarz J, Cualing HD
   A case of acute basophilic leukemia arising from chronic myelogenous leukemia with development of t(7;8)(q32;q13).
   Cancer Genet Cytogenet. 2008;182:46-9.
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8. OREN H , Yilmaz S, Sercan Z, Demircioglu F, et al
   Isolated myelosarcoma development in an adolescent chronic myeloid leukemia patient with t(9;22)(q34;q11.2), +8, +14, +21, and der(1)(p36).
   Cancer Genet Cytogenet. 2008;182:43-45.
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9. AMARE KADAM PS , Raje GC, Pais AP, Banavali S, et al
   Coexistence of ETV6/RUNX1 and MLL aberrations in B-cell precursor acute lymphoblastic leukemia discloses a small subclass of BCP-ALL.
   Cancer Genet Cytogenet. 2008;182:27-32.
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   March 2008
10. IMPERA L , Albano F, Mancini M, Aventin A, et al
    Similar mechanisms formed ring markers containing chromosome 12 pericentromeric region in two patients with therapy-related acute myeloid leukemia.
    Cancer Genet Cytogenet. 2008;181:131-7.
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11. ZEIDAN A , Phatak P
    Acquired biclonal chromosome X aberrations without autosomal chromosomal anomalies in acute myeloid leukemia.
    Cancer Genet Cytogenet. 2008;181:125-30.
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    February 2008
12. BALATZENKO G , Guenova M, Stoimenov A, Jotov G, et al
    Philadelphia chromosome-positive chronic myeloid leukemia with p190(BCR-ABL) rearrangement, overexpression of the EVI1 gene, and extreme thrombocytosis: a case report.
    Cancer Genet Cytogenet. 2008;181:75-7.
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13. BENNOUR A , Sennana H, Laatiri MA, Khelif A, et al
    A masked BCR/ABL rearrangement in a case of chronic myeloid leukemia with translocation t(3;9)(p14;q34).
    Cancer Genet Cytogenet. 2008;181:72-4.
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14. LI T , Xue Y, Zhang J, Chen S, et al
    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).
    Cancer Genet Cytogenet. 2008;181:55-9.
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15. LEE J , Lu X, Shin ES, Kern WF, et al
    A novel subtelomeric translocation t(5;9) and a deletion of the RB1 gene in a patient with acute myeloid leukemia (AML-M0).
    Cancer Genet Cytogenet. 2008;181:36-9.
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16. BETTIO D , Venci A, Sarina B
    Near-tetraploid karyotype with an isochromosome 17q as the sole structural chromosomal rearrangement in a case of testicular granulocytic sarcoma.
    Cancer Genet Cytogenet. 2008;181:69-71.
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17. PARKER H , Cheung KL, Robinson HM, Harrison CJ, et al
    Cytogenetic and genomic characterization of cell line ARH77.
    Cancer Genet Cytogenet. 2008;181:40-5.
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    January 2008
18. NADAL N , Stephan JL, Cornillon J, Guyotat D, et al
    RUNX1 rearrangements in acute myeloblastic leukemia relapsing after hematopoietic stem cell transplantation.
    Cancer Genet Cytogenet. 2008;180:168-9.
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19. SNIJDER S , Mellink CH, van der Lelie H
    Translocation (2;11)(q37;q23) in therapy-related myelodysplastic syndrome after treatment for acute promyelocytic leukemia.
    Cancer Genet Cytogenet. 2008;180:149-52.
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20. HAMURCU Z , Donmez-Altuntas H, Patiroglu T
    Basal level micronucleus frequency in stimulated lymphocytes of untreated patients with leukemia.
    Cancer Genet Cytogenet. 2008;180:140-4.
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21. YAGYU S , Morimoto A, Kakazu N, Tamura S, et al
    Late appearance of a Philadelphia chromosome in a patient with therapy-related acute myeloid leukemia and high expression of EVI1.
    Cancer Genet Cytogenet. 2008;180:115-20.
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22. AHMAD F , Kokate P, Chheda P, Dalvi R, et al
    Molecular cytogenetic findings in a three-way novel variant of t(1;8;21)(p35;q22;q22): a unique relocation of the AML1/ETO fusion gene 1p35 in AML-M2.
    Cancer Genet Cytogenet. 2008;180:153-7.
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23. PEREZ-VERA P , Montero-Ruiz O, Frias S, Rivera-Luna R, et al
    Multiple copies of RUNX1: description of 14 new patients, follow-up, and a review of the literature.
    Cancer Genet Cytogenet. 2008;180:129-34.
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24. GOZZETTI A , Bocchia M, Crupi R, Calabrese S, et al
    Concomitant chronic myeloid leukemia and chronic lymphocytic leukemia: a different clonal origin shown by molecular cytogenetics.
    Cancer Genet Cytogenet. 2008;180:83-4.
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25. KAWAMURA M , Kaku H, Taketani T, Taki T, et al
    Mutations of GATA1, FLT3, MLL-partial tandem duplication, NRAS, and RUNX1 genes are not found in a 7-year-old Down syndrome patient with acute myeloid leukemia (FAB-M2) having a good prognosis.
    Cancer Genet Cytogenet. 2008;180:74-8.
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26. PHAN CL , Megat Baharuddin PJ, Chin LP, Zakaria Z, et al
    Amplification of BCR-ABL and t(3;21) in a patient with blast crisis of chronic myelogenous leukemia.
    Cancer Genet Cytogenet. 2008;180:60-4.
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27. HELIAS C , Struski S, Gervais C, Leymarie V, et al
    Polycythemia vera transforming to acute myeloid leukemia and complex abnormalities including 9p homogeneously staining region with amplification of MLLT3, JMJD2C, JAK2, and SMARCA2.
    Cancer Genet Cytogenet. 2008;180:51-5.
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28. PETIT A , Radford I, Waill MC, Romana S, et al
    NUP98-NSD1 fusion by insertion in acute myeloblastic leukemia.
    Cancer Genet Cytogenet. 2008;180:43-6.
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29. MANOLA KN , Georgakakos VN, Margaritis D, Stavropoulou C, et al
    Disruption of the ETV6 gene as a consequence of a rare translocation (12;12)(p13;q13) in treatment-induced acute myeloid leukemia after breast cancer.
    Cancer Genet Cytogenet. 2008;180:37-42.
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    December 2007
30. ZHU W , Sun Z, Zhai Z, Ding K, et al
    A novel t(3;19)(p21;p13) in a patient with acute myelocytic leukemia.
    Cancer Genet Cytogenet. 2007;179:165-6.
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31. GOHRING G , Erlacher M, van Buiren M, Juttner E, et al
    Mesenteric chloroma with t(16;16) followed by acute myelomonocytic leukemia with clonal evolution.
    Cancer Genet Cytogenet. 2007;179:162-4.
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32. DE BRAEKELEER E , Douet-Guilbert N, Le Bris MJ, Morel F, et al
    Translocation 3;21, trisomy 8, and duplication of the Philadelphia chromosome: a rare but recurrent cytogenetic pathway in the blastic phase of chronic myeloid leukemia.
    Cancer Genet Cytogenet. 2007;179:159-61.
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33. METZKE-HEIDEMANN S , Harder L, Gesk S, Grimm W, et al
    The short arm of chromosome 18 is a recurrent integration site of a supernumerary BCR/ABL gene fusion in chronic myeloid leukemia.
    Cancer Genet Cytogenet. 2007;179:156-8.
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34. PARK TS , Song J, Lee KA, Lee SG, et al
    A der(1;15)(q10;q10) is a rare nonrandom whole-arm translocation in patients with acute lymphoblastic leukemia.
    Cancer Genet Cytogenet. 2007;179:132-5.
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    November 2007
35. TAKEUCHI M , Katayama Y, Okamura A, Yamamoto K, et al
    Chronic myeloid leukemia with a rare variant BCR-ABL translocation: t(9;22;21)(q34;q11.2;q11.2).
    Cancer Genet Cytogenet. 2007;179:85-7.
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36. LAHIRI O , Harris S, Packham G, Howell M, et al
    p53 pathway gene single nucleotide polymorphisms and chronic lymphocytic leukemia.
    Cancer Genet Cytogenet. 2007;179:36-44.
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37. SPENCER DV , Cavalier M, Kalpatthi R, Quigley DI, et al
    Inverted and deleted chromosome 16 with deletion of 3'CBFB identified by fluorescence in situ hybridization.
    Cancer Genet Cytogenet. 2007;179:82-4.
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38. MALLO M , Espinet B, Salido M, Ferrer A, et al
    Gain of multiple copies of the CBFB gene: a new genetic aberration in a case of granulocytic sarcoma.
    Cancer Genet Cytogenet. 2007;179:62-5.
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    October 2007
39. UDAYAKUMAR AM , Pathare AV, Alkindi S, Raeburn JA, et al
    Biphenotypic leukemia with interstitial del(9)(q22q32) as a sole abnormality.
    Cancer Genet Cytogenet. 2007;178:170-2.
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40. ABLA O , Dror Y, Shago M
    Translocation (X;10) in a child with therapy-related acute myeloid leukemia following chemotherapy for Ewing's Sarcoma.
    Cancer Genet Cytogenet. 2007;178:168-9.
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41. ABDELHALEEM M , Shago M, Sayeh E, Abla O, et al
    Childhood myeloid/natural killer precursor acute leukemia with novel chromosomal aberrations der(5)t(4;5)(q31;q31.3) and t(14;17)(q32;q23).
    Cancer Genet Cytogenet. 2007;178:141-3.
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42. GINDINA T , Kondakova E, Mamaev N
    Supernumerary ring chromosomes accompanied with near-tetraploidy following chemotherapy and cranial radiation in a girl with a relapsed acute lymphoblastic leukemia.
    Cancer Genet Cytogenet. 2007;178:82-4.
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43. PODGORNIK H , Debeljak M, Zontar D, Cernelc P, et al
    RUNX1 amplification in lineage conversion of childhood B-cell acute lymphoblastic leukemia to acute myelogenous leukemia.
    Cancer Genet Cytogenet. 2007;178:77-81.
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44. BIZARRO S , Cerveira N, Correia C, Lisboa S, et al
    Molecular characterization of a rare MLL-AF4 (MLL-AFF1) fusion rearrangement in infant leukemia.
    Cancer Genet Cytogenet. 2007;178:61-4.
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45. GAO YJ , Zhu XH, Yang Y, Wu Y, et al
    Prevalence of ETV6-RUNX1 fusion gene in children with acute lymphoblastic leukemia in China.
    Cancer Genet Cytogenet. 2007;178:57-60.
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46. GUIMARAES VAZ DE CAMPOS M , Montesano FT, Rodrigues MM, de Lourdes Lopes Ferrari Chauffaille M, et al
    Clinical implications of der(9q) deletions detected through dual-fusion fluorescence in situ hybridization in patients with chronic myeloid leukemia.
    Cancer Genet Cytogenet. 2007;178:49-56.
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47. ZHANG L , Alsabeh R, Mecucci C, La Starza R, et al
    Rare t(1;11)(q23;p15) in therapy-related myelodysplastic syndrome evolving into acute myelomonocytic leukemia: a case report and review of the literature.
    Cancer Genet Cytogenet. 2007;178:42-8.
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    September 2007
48. ORCIUOLO E , Buda G, Galimberti S, Sordi E, et al
    Concomitant appearance of trisomy 8 and isochromosome 17q in a Philadelphia-positive clone in a patient with chronic myeloid leukemia in chronic phase: an alarm for changing therapeutic strategy.
    Cancer Genet Cytogenet. 2007;177:166-7.
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49. TAKAHASHI T , Watanabe M, Minato M, Yoshimoto M, et al
    A novel t(12;15)(q22;q13) in a patient with acute monoblastic leukemia.
    Cancer Genet Cytogenet. 2007;177:164-5.
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50. ALVAREZ Y , Caballin MR, Gaitan S, Perez A, et al
    Presenting features of 201 children with acute lymphoblastic leukemia: Comparison according to presence or absence of ETV6/RUNX1 rearrangement.
    Cancer Genet Cytogenet. 2007;177:161-3.
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51. PARK TS , Song J, Lee KA, Lee SG, et al
    t(5;12)(q13;p13) in acute myeloid leukemia with preceding granulocytic sarcoma.
    Cancer Genet Cytogenet. 2007;177:158-60.
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52. SAIT SN , Claydon MA, Conroy JM, Nowak NJ, et al
    Translocation (4;11)(p12;q23) with rearrangement of FRYL and MLL in therapy-related acute myeloid leukemia.
    Cancer Genet Cytogenet. 2007;177:143-6.
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53. USTUN C , Kalla A, Bollag RJ, Manaloo E, et al
    Relapsed acute myelogenous leukemia occurring after 18 years with recurrent novel chromosomal abnormality t(18;22)(q23;q11.2).
    Cancer Genet Cytogenet. 2007;177:135-8.
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54. DAI H , Xue Y, Pan J, Wu Y, et al
    Two novel translocations disrupt the RUNX1 gene in acute myeloid leukemia.
    Cancer Genet Cytogenet. 2007;177:120-4.
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55. UDAYAKUMAR AM , Pathare AV, Al-Kindi S, Khan H, et al
    Cytogenetic, morphological, and immunophenotypic patterns in Omani patients with de novo acute myeloid leukemia.
    Cancer Genet Cytogenet. 2007;177:89-94.
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56. CHOI WT , Folsom MR, Azim MF, Meyer C, et al
    C/EBPbeta suppression by interruption of CUGBP1 resulting from a complex rearrangement of MLL.
    Cancer Genet Cytogenet. 2007;177:108-14.
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    August 2007
57. GOZZETTI A , Calabrese S, Raspadori D, Crupi R, et al
    Concomitant t(4;11) and t(1;19) in a patient with biphenotypic acute leukemia.
    Cancer Genet Cytogenet. 2007;177:81-2.
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58. SHIN MG , Lee JS, Cho D, Kim SH, et al
    Adult T-cell leukemia/lymphoma with a complex karyotype and central nervous system involvement.
    Cancer Genet Cytogenet. 2007;177:78-80.
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59. CHAUFFAILLE MDE L , Sugayama SM, Damiani D, Vieira JG, et al
    Chronic myeloid leukemia in an XX male.
    Cancer Genet Cytogenet. 2007;177:73-4.
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60. WEISSER M , Haferlach C, Haferlach T, Schnittger S, et al
    Feasibility of using the combined MDS-EVI1/EVI1 gene expression as an alternative molecular marker in acute myeloid leukemia: a report of four cases.
    Cancer Genet Cytogenet. 2007;177:64-9.
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61. STEINBACH D , Pfaffendorf N, Wittig S, Gruhn B, et al
    PRAME expression is not associated with down-regulation of retinoic acid signaling in primary acute myeloid leukemia.
    Cancer Genet Cytogenet. 2007;177:51-4.
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62. LENNON PA , Abruzzo LV, Medeiros LJ, Cromwell C, et al
    Aberrant EVI1 expression in acute myeloid leukemias associated with the t(3;8)(q26;q24).
    Cancer Genet Cytogenet. 2007;177:37-42.
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    July 2007
63. OO TH
    Trisomies 3 and 18 in a newly diagnosed chronic lymphocytic leukemia.
    Cancer Genet Cytogenet. 2007;176:175.
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64. ZEIDAN A , Kakati S, Anderson B, Barcos M, et al
    Monosomy 7 in t(9;22)-negative cells during nilotinib therapy in an imatinib-resistant chronic myeloid leukemia case.
    Cancer Genet Cytogenet. 2007;176:169-71.
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65. LI X , Yang J, Chen X, Liu J, et al
    A report of early cytogenetic response to imatinib in two patients with chronic myeloid leukemia at accelerated phase and carrying the e19a2 BCR-ABL transcript.
    Cancer Genet Cytogenet. 2007;176:166-8.
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66. MELICHERCIKOVA J , Brezinova J, Zemanova Z, Cermak J, et al
    Molecular cytogenetic analysis of complex karyotypes with derivative chromosome der(1)t(1;5) found in two patients with myeloid leukemia.
    Cancer Genet Cytogenet. 2007;176:150-5.
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67. YAMAMOTO K , Okamura A, Kawano H, Katayama Y, et al
    A novel t(8;18)(q13;q21) in acute monocytic leukemia evolving from constitutional trisomy 8 mosaicism.
    Cancer Genet Cytogenet. 2007;176:144-9.
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68. HIDAKA E , Tanaka M, Matsuda K, Ishikawa-Matsumura M, et al
    A complex karyotype, including a three-way translocation generating a NUP98-HOXD13 transcript, in an infant with acute myeloid leukemia.
    Cancer Genet Cytogenet. 2007;176:137-43.
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69. MIYAZAKI K , Kikukawa M, Kiuchi A, Shin K, et al
    Complex translocations derived stepwise from standard t(15;17) in a patient with variant acute promyelocytic leukemia.
    Cancer Genet Cytogenet. 2007;176:127-30.
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70. BERNHEIM A , Dessen P, Lazar V, Auger N, et al
    Cryptic del(13q14.2) and physiological deletions of immunoglobulin genes detected by high-resolution array comparative genomic hybridization in a patient with indolent chronic lymphocytic leukemia.
    Cancer Genet Cytogenet. 2007;176:89-91.
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71. VAN BINSBERGEN E , de Weerdt O, Buijs A
    A new subtype of MLL-SEPT2 fusion transcript in therapy-related acute myeloid leukemia with t(2;11)(q37;q23): a case report and literature review.
    Cancer Genet Cytogenet. 2007;176:72-5.
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72. CRESCENZI B , La Starza R, Nozzoli C, Ciolli S, et al
    Molecular cytogenetic findings in a four-way t(1;12;5;12)(p36;p13;q33;q24) underlying the ETV6-PDGFRB fusion gene in chronic myelomonocytic leukemia.
    Cancer Genet Cytogenet. 2007;176:67-71.
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73. YAMAMOTO K , Yakushijin K, Kawamori Y, Minagawa K, et al
    Translocation (7;9)(q22;q34) in therapy-related myelodysplastic syndrome after allogeneic bone marrow transplantation for acute myeloblastic leukemia.
    Cancer Genet Cytogenet. 2007;176:61-6.
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74. ROTHLISBERGER B , Heizmann M, Bargetzi MJ, Huber AR, et al
    TRIB1 overexpression in acute myeloid leukemia.
    Cancer Genet Cytogenet. 2007;176:58-60.
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75. LESSARD M , Helias C, Struski S, Perrusson N, et al
    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?
    Cancer Genet Cytogenet. 2007;176:1-21.
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    June 2007
76. GOZZETTI A , Calabrese S, Crupi R, Zaja F, et al
    Trisomy 8 in chronic lymphocytic leukemia: a report of two cases.
    Cancer Genet Cytogenet. 2007;175:175-6.
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77. COOLEY LD , Chenevert S, Shuster JJ, Johnston DA, et al
    Prognostic significance of cytogenetically detected chromosome 21 anomalies in childhood acute lymphoblastic leukemia: a Pediatric Oncology Group study.
    Cancer Genet Cytogenet. 2007;175:117-24.
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78. HERRY A , Douet-Guilbert N, Morel F, Le Bris MJ, et al
    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.
    Cancer Genet Cytogenet. 2007;175:125-31.
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    May 2007
79. LA STARZA R , Crescenzi B, Pierini V, Romoli S, et al
    A common 93-kb duplicated DNA sequence at 1q21.2 in acute lymphoblastic leukemia and Burkitt lymphoma.
    Cancer Genet Cytogenet. 2007;175:73-6.
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80. SANCHEZ J , Aventin A
    Detection of chromosomal abnormalities in chronic lymphocytic leukemia increased by interphase fluorescence in situ hybridization in tetradecanoylphorbol acetate-stimulated peripheral blood cells.
    Cancer Genet Cytogenet. 2007;175:57-60.
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81. BACHER U , Haferlach T, Kern W, Harich HD, et al
    A case of chronic myeloproliferative syndrome followed by precursor T-cell acute lymphoblastic leukemia.
    Cancer Genet Cytogenet. 2007;175:52-6.
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82. KNUDSON RA , Shearer BM, Ketterling RP
    Automated Duet spot counting system and manual technologist scoring using dual-fusion fluorescence in situ hybridization (D-FISH) strategy: comparison and application to FISH minimal residual disease testing in patients with chronic myeloid leukemia.
    Cancer Genet Cytogenet. 2007;175:8-18.
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83. GOHRING G , Lange K, Atta J, Krauter J, et al
    Cryptic t(15;17) in a patient with AML M3 and a complex karyotype.
    Cancer Genet Cytogenet. 2007;175:77-80.
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    April 2007
84. TIRADO CA , Meloni-Ehrig AM, Edwards T, Scheerle J, et al
    Cryptic ins(4;11)(q21;q23q23) detected by fluorescence in situ hybridization: a variant of t(4;11)(q21;q23) in an infant with a precursor B-cell acute lymphoblastic leukemia report of a second case.
    Cancer Genet Cytogenet. 2007;174:166-9.
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85. CHEN CC , Yang CF, Lee KD, You JY, et al
    Complex karyotypes confer a poor survival in adult acute myeloid leukemia with unfavorable cytogenetic abnormalities.
    Cancer Genet Cytogenet. 2007;174:138-146.
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86. PAJUELO-GAMEZ JC , Cervera J, Garcia-Casado Z, Mena-Duran AV, et al
    MLL amplification in acute myeloid leukemia.
    Cancer Genet Cytogenet. 2007;174:127-31.
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87. ALBANO F , Anelli L, Zagaria A, Archidiacono N, et al
    "Home-brew" FISH assay shows higher efficiency than BCR-ABL dual color, dual fusion probe in detecting microdeletions and complex rearrangements associated with t(9;22) in chronic myeloid leukemia.
    Cancer Genet Cytogenet. 2007;174:121-6.
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