156 related articles for article (PubMed ID: 11063802)
1. Isochromosome (7)(q10) in Shwachman syndrome without MDS/AML and role of chromosome 7 anomalies in myeloproliferative disorders.
Maserati E; Minelli A; Olivieri C; Bonvini L; Marchi A; Bozzola M; Danesino C; Scappaticci S; Pasquali F
Cancer Genet Cytogenet; 2000 Sep; 121(2):167-71. PubMed ID: 11063802
[TBL] [Abstract][Full Text] [Related]
2. Discordant detection of monosomy 7 by GTG-banding and FISH in a patient with Shwachman-Diamond syndrome without evidence of myelodysplastic syndrome or acute myelogenous leukemia.
Sokolic RA; Ferguson W; Mark HF
Cancer Genet Cytogenet; 1999 Dec; 115(2):106-13. PubMed ID: 10598142
[TBL] [Abstract][Full Text] [Related]
3. The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies.
Maserati E; Pressato B; Valli R; Minelli A; Sainati L; Patitucci F; Marletta C; Mastronuzzi A; Poli F; Lo Curto F; Locatelli F; Danesino C; Pasquali F
Br J Haematol; 2009 Apr; 145(2):190-7. PubMed ID: 19222471
[TBL] [Abstract][Full Text] [Related]
4. Malignant myeloid transformation with isochromosome 7q in Shwachman-Diamond syndrome.
Dror Y; Squire J; Durie P; Freedman MH
Leukemia; 1998 Oct; 12(10):1591-5. PubMed ID: 9766504
[TBL] [Abstract][Full Text] [Related]
5. The isochromosome i(7)(q10) carrying c.258+2t>c mutation of the SBDS gene does not promote development of myeloid malignancies in patients with Shwachman syndrome.
Minelli A; Maserati E; Nicolis E; Zecca M; Sainati L; Longoni D; Lo Curto F; Menna G; Poli F; De Paoli E; Cipolli M; Locatelli F; Pasquali F; Danesino C
Leukemia; 2009 Apr; 23(4):708-11. PubMed ID: 19148133
[TBL] [Abstract][Full Text] [Related]
6. Shwachman syndrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies.
Maserati E; Minelli A; Pressato B; Valli R; Crescenzi B; Stefanelli M; Menna G; Sainati L; Poli F; Panarello C; Zecca M; Curto FL; Mecucci C; Danesino C; Pasquali F
Genes Chromosomes Cancer; 2006 Apr; 45(4):375-82. PubMed ID: 16382447
[TBL] [Abstract][Full Text] [Related]
7. Intermittent 20q- and consistent i(7q) in a patient with Shwachman-Diamond syndrome.
Smith A; Shaw PJ; Webster B; Lammi A; Gaskin K; Diaz S; Sharma P
Pediatr Hematol Oncol; 2002; 19(7):525-8. PubMed ID: 12217199
[TBL] [Abstract][Full Text] [Related]
8. Does isochromosome 7q mandate bone marrow transplant in children with Shwachman-Diamond syndrome?
Cunningham J; Sales M; Pearce A; Howard J; Stallings R; Telford N; Wilkie R; Huntly B; Thomas A; O'Marcaigh A; Will A; Pratt N
Br J Haematol; 2002 Dec; 119(4):1062-9. PubMed ID: 12472589
[TBL] [Abstract][Full Text] [Related]
9. Monitoring the isochromosome i(7)(q10) in the bone marrow of patients with Shwachman syndrome by real-time quantitative PCR.
Porta G; Mattarucchi E; Maserati E; Pressato B; Valli R; Morerio C; Zecca M; Panarello C; Locatelli F; Lo Curto F; Pasquali F
J Pediatr Hematol Oncol; 2007 Mar; 29(3):163-5. PubMed ID: 17356395
[TBL] [Abstract][Full Text] [Related]
10. Clonal evolution in marrows of patients with Shwachman-Diamond syndrome: a prospective 5-year follow-up study.
Dror Y; Durie P; Ginzberg H; Herman R; Banerjee A; Champagne M; Shannon K; Malkin D; Freedman MH
Exp Hematol; 2002 Jul; 30(7):659-69. PubMed ID: 12135662
[TBL] [Abstract][Full Text] [Related]
11. Novel recurrent chromosome anomalies in Shwachman-Diamond syndrome.
Valli R; De Paoli E; Nacci L; Frattini A; Pasquali F; Maserati E
Pediatr Blood Cancer; 2017 Aug; 64(8):. PubMed ID: 28130858
[TBL] [Abstract][Full Text] [Related]
12. Myeloid neoplasms with isolated isochromosome 17q represent a clinicopathologic entity associated with myelodysplastic/myeloproliferative features, a high risk of leukemic transformation, and wild-type TP53.
Kanagal-Shamanna R; Bueso-Ramos CE; Barkoh B; Lu G; Wang S; Garcia-Manero G; Vadhan-Raj S; Hoehn D; Medeiros LJ; Yin CC
Cancer; 2012 Jun; 118(11):2879-88. PubMed ID: 22038701
[TBL] [Abstract][Full Text] [Related]
13. Mutation analysis of SBDS in pediatric acute myeloblastic leukemia.
Majeed F; Jadko S; Freedman MH; Dror Y
Pediatr Blood Cancer; 2005 Dec; 45(7):920-4. PubMed ID: 16007594
[TBL] [Abstract][Full Text] [Related]
14. SBDS mutations and isochromosome 7q in a patient with Shwachman-Diamond syndrome: no predisposition to malignant transformation?
Mellink CH; Alders M; van der Lelie H; Hennekam RH; Kuijpers TW
Cancer Genet Cytogenet; 2004 Oct; 154(2):144-9. PubMed ID: 15474150
[TBL] [Abstract][Full Text] [Related]
15. Chromosomal aberrations in congenital bone marrow failure disorders--an early indicator for leukemogenesis?
Göhring G; Karow A; Steinemann D; Wilkens L; Lichter P; Zeidler C; Niemeyer C; Welte K; Schlegelberger B
Ann Hematol; 2007 Oct; 86(10):733-9. PubMed ID: 17653548
[TBL] [Abstract][Full Text] [Related]
16. Familial partial monosomy 7 and myelodysplasia: different parental origin of the monosomy 7 suggests action of a mutator gene.
Minelli A; Maserati E; Giudici G; Tosi S; Olivieri C; Bonvini L; De Filippi P; Biondi A; Lo Curto F; Pasquali F; Danesino C
Cancer Genet Cytogenet; 2001 Jan; 124(2):147-51. PubMed ID: 11172908
[TBL] [Abstract][Full Text] [Related]
17. Transient myelodysplastic syndrome associated with isochromosome 7q abnormality.
Leung EW; Woodman RC; Roland B; Abdelhaleem M; Freedman MH; Dror Y
Pediatr Hematol Oncol; 2003; 20(7):539-45. PubMed ID: 12959859
[TBL] [Abstract][Full Text] [Related]
18. Numerical chromosomal changes and risk of development of myelodysplastic syndrome--acute myeloid leukemia in patients with Fanconi anemia.
Mehta PA; Harris RE; Davies SM; Kim MO; Mueller R; Lampkin B; Mo J; Myers K; Smolarek TA
Cancer Genet Cytogenet; 2010 Dec; 203(2):180-6. PubMed ID: 21156231
[TBL] [Abstract][Full Text] [Related]
19. Chromosome 20q deletion and progression to monosomy 7 in a patient with Shwachman-Diamond syndrome without MDS/AML.
Raj AB; Bertolone SJ; Barch MJ; Hersh JH
J Pediatr Hematol Oncol; 2003 Jun; 25(6):508-9. PubMed ID: 12794535
[No Abstract] [Full Text] [Related]
20. Isochromosome 5p and related anomalies: a novel recurrent chromosome abnormality in myeloid disorders.
Herry A; Douet-Guilbert N; Morel F; Le Bris MJ; Guéganic N; Berthou C; De Braekeleer M
Cancer Genet Cytogenet; 2010 Jul; 200(2):134-9. PubMed ID: 20620596
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
