108 related articles for article (PubMed ID: 25932448)
1. A novel case of extreme thrombocytosis in acute myeloid leukemia associated with isochromosome 17q and copy neutral loss of heterozygosity.
You E; Cho SY; Yang JJ; Lee HJ; Lee WI; Lee J; Cho KS; Cho EH; Park TS
Ann Lab Med; 2015 May; 35(3):366-9. PubMed ID: 25932448
[No Abstract] [Full Text] [Related]
2. Case report of isochromosome 17q in acute myeloid leukemia with myelodysplasia-related changes after treatment with a hypomethylating agent.
Sousa JC; Germano RT; Castro CC; Magalhaes SM; Pinheiro RF
Genet Mol Res; 2012 Aug; 11(3):2045-50. PubMed ID: 22911588
[TBL] [Abstract][Full Text] [Related]
3. Near-tetraploid karyotype with an isochromosome 17q as the sole structural chromosomal rearrangement in a case of testicular granulocytic sarcoma.
Bettio D; Venci A; Sarina B
Cancer Genet Cytogenet; 2008 Feb; 181(1):69-71. PubMed ID: 18262059
[No Abstract] [Full Text] [Related]
4. Double supernumerary isochromosome 4p in acute myelomonocytic leukemia.
Soriani S; Marbello L; Colosimo A; Scarpati B; Grillo G; Cesana C
Leuk Res; 2010 Dec; 34(12):e342-4. PubMed ID: 20863564
[No Abstract] [Full Text] [Related]
5. Gain of an isochromosome 5p: a rare recurrent abnormality in acute myeloid leukemia.
Panani AD
In Vivo; 2006; 20(3):359-60. PubMed ID: 16724670
[TBL] [Abstract][Full Text] [Related]
6. A case of isodicentric 7p as sole abnormality in a patient with acute myeloid leukemia.
Beverstock GC; de Meijer PH; ten Bokkel Huinink D; Pruijt JF; den Ottolander GJ; Wessels HW; Mollevanger P
Cancer Genet Cytogenet; 1996 Jul; 89(2):132-5. PubMed ID: 8697419
[TBL] [Abstract][Full Text] [Related]
7. The landscape of myeloid neoplasms with isochromosome 17q discloses a specific mutation profile and is characterized by an accumulation of prognostically adverse molecular markers.
Meggendorfer M; Haferlach C; Zenger M; Macijewski K; Kern W; Haferlach T
Leukemia; 2016 Jul; 30(7):1624-7. PubMed ID: 26859077
[No Abstract] [Full Text] [Related]
8. Acute myeloid leukemia with mutated NPM1 demonstrating multilineage dysplasia and marked thrombocytosis.
Chen Y; Pourabdollah M; Chang H
Br J Haematol; 2017 Aug; 178(3):350. PubMed ID: 28677819
[No Abstract] [Full Text] [Related]
9. Development of minimally differentiated acute myeloblastic leukemia with novel isochromosome 18p and antecedent aplastic anemia.
Keung YK; Cobos E; Morgan D; Tonk V
Cancer Genet Cytogenet; 1996 Nov; 92(1):1-3. PubMed ID: 8956860
[TBL] [Abstract][Full Text] [Related]
10. A novel prognosis of acute myeloid leukemia: AML-M2 complicate with thrombocythemia after complete remission.
Chen YX; Li Y; Zhang LY; Liu B
Leuk Res; 2012 Aug; 36(8):e166-7. PubMed ID: 22579367
[No Abstract] [Full Text] [Related]
11. Concomitant isochromosome 17q and trisomy 14 in a patient with myelodysplastic syndrome in leukemic transformation.
Park TS; Song J; Lee JH; Kim JS; Yang WI; Choi JR
Ann Clin Lab Sci; 2009; 39(2):176-81. PubMed ID: 19429805
[TBL] [Abstract][Full Text] [Related]
12. Isochromosome 17q in MDS: a marker of a distinct entity.
Pinheiro RF; Chauffaille Mde L; Silva MR
Cancer Genet Cytogenet; 2006 Apr; 166(2):189-90. PubMed ID: 16631479
[No Abstract] [Full Text] [Related]
13. Acute myeloid leukemia associated with t(1;3)(p36;q21) and extreme thrombocytosis: a clinical study with literature review.
Lim G; Kim MJ; Oh SH; Cho SY; Lee HJ; Suh JT; Lee J; Lee WI; Cho KS; Park TS
Cancer Genet Cytogenet; 2010 Dec; 203(2):187-92. PubMed ID: 21156232
[TBL] [Abstract][Full Text] [Related]
14. Single nucleotide polymorphism microarray analysis of karyotypically normal acute myeloid leukemia reveals frequent copy number neutral loss of heterozygosity.
Tyybäkinoja A; Elonen E; Vauhkonen H; Saarela J; Knuutila S
Haematologica; 2008 Apr; 93(4):631-2. PubMed ID: 18379011
[No Abstract] [Full Text] [Related]
15. A rare case of ICUS progressing to MDS with isolated isochromosome 17q and AML.
Ordonez Mazariegos EE; Dimopoulos YP
Blood; 2024 Feb; 143(5):473. PubMed ID: 38300608
[No Abstract] [Full Text] [Related]
16. A rare case with typical acute promyelocytic leukemia morphology associated with isolated isochromosome 17q without RARα rearrangement.
Duan Y; Nie J; Zhang Z; Zhou L; Zhu F; Zhang H; Zhu H; Shang W
Hematol Oncol Stem Cell Ther; 2013 Mar; 6(1):42-5. PubMed ID: 23664605
[TBL] [Abstract][Full Text] [Related]
17. Supernumerary isochromosome 4p in ANLL-M4 myelomonocytic type is associated with favorable prognosis.
Hoo JJ; Gregory SA; Jones B; Szego K
Cancer Genet Cytogenet; 1995 Feb; 79(2):127-9. PubMed ID: 7889503
[TBL] [Abstract][Full Text] [Related]
18. Isochromosome der(17)(q10)t(15;17) in acute promyelocytic leukemia resulting in an additional copy of the RARA-PML fusion gene: report of 4 cases and review of the literature.
Manola KN; Karakosta M; Sambani C; Terzoudi G; Pagoni M; Gatsa E; Papaioannou M
Acta Haematol; 2010; 123(3):162-70. PubMed ID: 20224268
[TBL] [Abstract][Full Text] [Related]
19. Single nucleotide polymorphism array-based karyotyping shows sequential genomic changes from monosomy to copy-neutral loss of heterozygosity of chromosome 7 and 20q deletion within a balanced translocation t(14;20) in AML.
Huh J; Mun YC; Seong CM; Chung WS
Cancer Genet; 2011 Dec; 204(12):682-6. PubMed ID: 22285021
[TBL] [Abstract][Full Text] [Related]
20. Acute myelocytic leukemia associated with thrombocytosis and inv 3(q21.3; q26.2) in a case of Grönbland-Strandberg syndrome.
Tasaka T; Nagai M; Kubota Y; Sasaki K; Murata M; Taoka T; Ikeda K; Tanaka T; Takahara J; Irino S
Leuk Res; 1992 Dec; 16(12):1187-90. PubMed ID: 1465027
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]