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Items: 1 to 20 of 114

1.

Essential thrombocythemia with myelofibrosis transformed into acute myeloid leukemia with der(1;15)(q10;q10): case report and literature review.

Charafeddine KM, Mahfouz RA, Zaatari GS, Ibrahim GY, Muwakkit SA, Najm ND, Farra CG.

Cancer Genet Cytogenet. 2010 Jul 1;200(1):28-33. doi: 10.1016/j.cancergencyto.2010.03.010. Review.

PMID:
20513531
2.

[Essential thrombocythemia in transformation to acute leukemia (FAB-M0) as a natural history from myelofibrosis with t(1;7)].

Hayashi S, Iwama H, Uchida Y, Kawakubo K, Inatomi Y, Nagasu M, Miyazawa K, Ohyashiki JH, Ohyashiki K, Toyama K.

Rinsho Ketsueki. 1997 May;38(5):445-7. Japanese.

PMID:
9194391
3.

De novo appearance of der(1;7)(q10;p10) is associated with leukemic transformation and unfavorable prognosis in essential thrombocythemia.

Hsiao HH, Ito Y, Sashida G, Ohyashiki JH, Ohyashiki K.

Leuk Res. 2005 Nov;29(11):1247-52. Epub 2005 Apr 14.

PMID:
16164981
4.

Insertion (4;11)(q27;q24q21) in a patient with essential thrombocythemia with progression to myelofibrosis.

Gargallo P, Hagemeijer A, Vassallu P, Kornblihtt L, Heller P, Molinas F, Larripa I.

Cancer Genet Cytogenet. 2004 Oct 1;154(1):72-6.

PMID:
15381377
5.

Chromosome 11 rearrangement at band 11q21 in a patient with essential thrombocythemia.

Nakamura H, Hayashibara T, Kawachi T, Nagai K, Matsuo T, Sadamori N, Tomonaga M.

Cancer Genet Cytogenet. 1992 Jan;58(1):105-7. Review.

PMID:
1728943
6.

[An acute leukemia case with complex karyotype abnormalities and marked thrombocythemia].

Okamura T, Hayakawa H, Sumida I, Hanada M, Nakasato S, Takeshita M, Ohgami A, Kikuchi M, Kamada N.

Rinsho Ketsueki. 1987 Nov;28(11):2023-8. Japanese. No abstract available.

PMID:
3482113
7.

Derivative (1;18)(q10;q10) in essential thrombocythemia.

Azuma T, Yamanouchi J, Inoue K, Kohno M, Narumi H, Fujiwara H, Yakushijin Y, Hato T, Yasukawa M.

Cancer Genet Cytogenet. 2010 May;199(1):62-4. doi: 10.1016/j.cancergencyto.2010.02.001.

PMID:
20417872
8.

Promyelocytic blast crisis of Philadelphia-positive thrombocythemia with translocations (9;22) and (15;17).

Laï JL, Fenaux P, Zandecki M, Savary JB, Estienne MH, Jouet JP, Bauters F, Deminatti M.

Cancer Genet Cytogenet. 1987 Dec;29(2):311-4.

PMID:
3479236
9.

Frequency of structural abnormalities of the long arm of chromosome 12 in myelofibrosis with myeloid metaplasia.

Andrieux J, Demory JL, Morel P, Plantier I, Dupriez B, Caulier MT, Bauters F, Laï JL.

Cancer Genet Cytogenet. 2002 Aug;137(1):68-71.

PMID:
12377417
10.

[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;25(5):579-82. Chinese.

PMID:
18841577
11.

A novel t(2;17) in transformation of essential thrombocythemia to acute myelocytic leukemia.

Lazarevic VLj, Tomin D, Jankovic GM, Antic D, Dencic M, Gotic M, Boskovic D.

Cancer Genet Cytogenet. 2004 Jan 1;148(1):77-9.

PMID:
14697645
12.

Chromosome aberrations including der(6)t(2;6)(p15;p21.3) and der(22)t(3;22)(p21;p11) in the evolution of essential thrombocythemia to myelofibrosis with myeloid metaplasia.

Lazarevic V, Andersson C, Wahlin A, Golovleva I.

Cancer Genet Cytogenet. 2006 Feb;165(1):87-9. No abstract available.

PMID:
16490605
13.

Progression of essential thrombocythemia to blastic crisis via idiopathic myelofibrosis.

Emilia G, Sacchi S, Temperani P, Longo R, Vecchi A.

Leuk Lymphoma. 1993 Mar;9(4-5):423-6.

PMID:
8348078
14.

A der(1;15)(q10;q10) is a rare nonrandom whole-arm translocation in patients with acute lymphoblastic leukemia.

Park TS, Song J, Lee KA, Lee SG, Yoon S, Kim JS, Lyu CJ, Choi JR.

Cancer Genet Cytogenet. 2007 Dec;179(2):132-5. Review.

PMID:
18036400
15.

[der(1;7) (q10;p10) in three patients with malignant hematologic disorders].

Yokoo H, Okada Y, Tominaga K, Tsuji M, Takagi T, Maseki N, Sakurai M, Kaneko Y.

Rinsho Ketsueki. 1992 Dec;33(12):1829-33. Japanese.

PMID:
1479694
16.
17.

Cytogenetic abnormalities in essential thrombocythemia: prevalence and prognostic significance.

Gangat N, Tefferi A, Thanarajasingam G, Patnaik M, Schwager S, Ketterling R, Wolanskyj AP.

Eur J Haematol. 2009 Jul;83(1):17-21. doi: 10.1111/j.1600-0609.2009.01246.x. Epub 2009 Feb 19.

PMID:
19236446
18.

Chromosome 1 abnormalities in myeloid malignancies: a literature survey and karyotype-phenotype associations.

Caramazza D, Hussein K, Siragusa S, Pardanani A, Knudson RA, Ketterling RP, Tefferi A.

Eur J Haematol. 2010 Mar;84(3):191-200. doi: 10.1111/j.1600-0609.2009.01392.x. Epub 2009 Nov 30. Review.

PMID:
20002154
19.

Complex chromosome translocations of standard t(8;21) and t(15;17) arise from a two-step mechanism as evidenced by fluorescence in situ hybridization analysis.

Calabrese G, Min T, Stuppia L, Powles R, Swansbury JG, Morizio E, Peila R, Donti E, Fioritoni G, Palka G.

Cancer Genet Cytogenet. 1996 Oct 1;91(1):40-5.

PMID:
8908165
20.

Mutation analysis of the FAS and TNFR apoptotic cascade genes in hematological malignancies.

Rozenfeld-Granot G, Toren A, Amariglio N, Brok-Simoni F, Rechavi G.

Exp Hematol. 2001 Feb;29(2):228-33.

PMID:
11166462

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