Publications

Found 4 results
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2012
E. E. Engel, Nogueira-Barbosa, M. H., Brassesco, M. S., Silva, G. E. B., Valera, E. T., Peria, F. M., Motta, T. C., and Tone, L. G., Osteosarcoma arising from osteochondroma of the tibia: case report and cytogenetic findings, vol. 11. pp. 448-454, 2012.
Bovée JV, Cleton-Jansen AM, Wuyts W, Caethoven G, et al. (1999). EXT-mutation analysis and loss of heterozygosity in sporadic and hereditary osteochondromas and secondary chondrosarcomas. Am. J. Hum. Genet. 65: 689-698.http://dx.doi.org/10.1086/302532PMid:10441575Bovée JV, Sakkers RJ, Geirnaerdt MJ, Taminiau AH, et al. (2002). Intermediate grade osteosarcoma and chondrosarcoma arising in an osteochondroma. A case report of a patient with hereditary multiple exostoses. J. Clin. Pathol. 55: 226- 229.http://dx.doi.org/10.1136/jcp.55.3.226PMid:11896078    PMCid:1769605Garrison RC, Unni KK, McLeod RA, Pritchard DJ, et al. (1982). Chondrosarcoma arising in osteochondroma. Cancer 49: 1890-1897.http://dx.doi.org/10.1002/1097-0142(19820501)49:9<1890::AID-CNCR2820490923>3.0.CO;2-UKhurana J, Abdul-Karim F and Bovée JVMG (2002). Osteochondroma. In: World Health Organization Classification of Tumours. Pathology and Genetics of Tumours of Soft Tissue and Bone (Fletcher CDM, Unni KK and Mertens F, eds.). IARC Press, Lyon, 234-236.Lamovec J, Spiler M and Jevtic V (1999). Osteosarcoma arising in a solitary osteochondroma of the fibula. Arch. Pathol. Lab. Med. 123: 832-834.PMid:10458834Lee KC, Davies AM and Cassar-Pullicino VN (2002). Imaging the complications of osteochondromas. Clin. Radiol. 57: 18-28.http://dx.doi.org/10.1053/crad.2001.0719PMid:11798198Meissner SA, Vieth V, August C and Winkelmann W (2006). Radiology-pathology conference: osteosarcoma in a cartilaginous exostosis of the femur. Clin. Imaging 30: 206-209.http://dx.doi.org/10.1016/j.clinimag.2005.12.026PMid:16632158Mertens F, Rydholm A, Kreicbergs A, Willen H, et al. (1994). Loss of chromosome band 8q24 in sporadic osteocartilaginous exostoses. Genes Chromosomes Cancer 9: 8-12.http://dx.doi.org/10.1002/gcc.2870090103Nezhad ST, Bagheri MH and Rakhshandero SH (2008). Osteosarcoma arising from a solitary osteochondroma of the tibia. IRCMJ 10: 341-343.Nishida Y, Isu K, Ueda T, Nishimoto Y, et al. (2009). Osteosarcoma in the elderly over 60 years: a multicenter study by the Japanese Musculoskeletal Oncology Group. J. Surg. Oncol. 100: 48-54.http://dx.doi.org/10.1002/jso.21287PMid:19384906Nojima T, Yamashiro K, Fujita M, Isu K, et al. (1991). A case of osteosarcoma arising in a solitary osteochondroma. Acta Orthop. Scand. 62: 290-292.http://dx.doi.org/10.3109/17453679108993613Sandberg AA and Bridge JA (2003). Updates on the cytogenetics and molecular genetics of bone and soft tissue tumors: osteosarcoma and related tumors. Cancer Genet. Cytogenet. 145: 1-30.http://dx.doi.org/10.1016/S0165-4608(03)00105-5Shaffer LG and Tommerup N (2005). ISCN 2005: An International System for Human Cytogenetic Nomenclature. Karger, Basel.Sjögren H, Orndal C, Tingby O, Meis-Kindblom JM, et al. (2004). Cytogenetic and spectral karyotype analyses of benign and malignant cartilage tumours. Int. J. Oncol. 24: 1385-1391.PMid:15138578Staals EL, Bacchini P, Mercuri M and Bertoni F (2007). Dedifferentiated chondrosarcomas arising in preexisting osteochondromas. J. Bone Joint. Surg. Am. 89: 987-993.http://dx.doi.org/10.2106/JBJS.F.00288PMid:17473135Zuntini M, Pedrini E, Parra A, Sgariglia F, et al. (2010). Genetic models of osteochondroma onset and neoplastic progression: evidence for mechanisms alternative to EXT genes inactivation. Oncogene 29: 3827-3834.http://dx.doi.org/10.1038/onc.2010.135PMid:20418910
2010
E. T. Valera, Brassesco, M. S., Scrideli, C. A., and Tone, L. G., Tetraploidization in Wilms tumor in an infant, vol. 9. pp. 1577-1581, 2010.
Betts DR, Koesters R, Pluss HJ and Niggli FK (1997). Routine karyotyping in Wilms tumor. Cancer Genet. Cytogenet. 96: 151-156.http://dx.doi.org/10.1016/S0165-4608(96)00318-4 Ganem NJ, Storchova Z and Pellman D (2007). Tetraploidy, aneuploidy and cancer. Curr. Opin. Genet. Dev. 17: 157-162.http://dx.doi.org/10.1016/j.gde.2007.02.011PMid:17324569 Gisselsson D, Hakanson U, Stoller P, Marti D, et al. (2008). When the genome plays dice: circumvention of the spindle assembly checkpoint and near-random chromosome segregation in multipolar cancer cell mitoses. PLoS One 3: e1871. Höglund M, Gisselsson D, Hansen GB and Mitelman F (2004). Wilms tumors develop through two distinct karyotypic pathways. Cancer Genet. Cytogenet. 150: 9-15.http://dx.doi.org/10.1016/j.cancergencyto.2003.08.017PMid:15041217 Iyer VK, Kapila K, Agarwala S, Dinda AK, et al. (1999). Wilms' tumor. Role of fine needle aspiration and DNA ploidy by image analysis in prognostication. Anal. Quant. Cytol. Histol. 21: 505-511.PMid:10626020 Li P, Yokomori K, Tsuchida Y, Fujita M, et al. (1995). Flow cytometric nuclear DNA content analysis of renal tumors in children: prognostic significance of nuclear DNA ploidy. Tumour Biol. 16: 385-393.http://dx.doi.org/10.1159/000217955PMid:7569685 Storchova Z and Pellman D (2004). From polyploidy to aneuploidy, genome instability and cancer. Nat. Rev. Mol. Cell Biol. 5: 45-54.http://dx.doi.org/10.1038/nrm1276PMid:14708009 Storchova Z and Kuffer C (2008). The consequences of tetraploidy and aneuploidy. J. Cell Sci. 121: 3859-3866.http://dx.doi.org/10.1242/jcs.039537PMid:19020304 Yildiz I, Jaffe N, Aksoy F and el-Naggar AK (1994). Regional DNA content heterogeneity in Wilms' tumor: incidence and potential clinical relevance. Anticancer Res. 14: 1365-1369.PMid:8067707