258 related articles for article (PubMed ID: 20233460)
1. Multiple osteochondromas: clinicopathological and genetic spectrum and suggestions for clinical management.
Hameetman L; Bovée JV; Taminiau AH; Kroon HM; Hogendoorn PC
Hered Cancer Clin Pract; 2004 Nov; 2(4):161-73. PubMed ID: 20233460
[TBL] [Abstract][Full Text] [Related]
2. Secondary peripheral chondrosarcoma evolving from osteochondroma as a result of outgrowth of cells with functional EXT.
de Andrea CE; Reijnders CM; Kroon HM; de Jong D; Hogendoorn PC; Szuhai K; Bovée JV
Oncogene; 2012 Mar; 31(9):1095-104. PubMed ID: 21804604
[TBL] [Abstract][Full Text] [Related]
3. Multiple osteochondromas.
Bovée JV
Orphanet J Rare Dis; 2008 Feb; 3():3. PubMed ID: 18271966
[TBL] [Abstract][Full Text] [Related]
4. Somatic loss of an EXT2 gene mutation during malignant progression in a patient with hereditary multiple osteochondromas.
Musso N; Caronia FP; Castorina S; Lo Monte AI; Barresi V; Condorelli DF
Cancer Genet; 2015 Mar; 208(3):62-7. PubMed ID: 25744876
[TBL] [Abstract][Full Text] [Related]
5. EXT-mutation analysis and loss of heterozygosity in sporadic and hereditary osteochondromas and secondary chondrosarcomas.
Bovée JV; Cleton-Jansen AM; Wuyts W; Caethoven G; Taminiau AH; Bakker E; Van Hul W; Cornelisse CJ; Hogendoorn PC
Am J Hum Genet; 1999 Sep; 65(3):689-98. PubMed ID: 10441575
[TBL] [Abstract][Full Text] [Related]
6. Intraosseous atypical chondroid tumor or chondrosarcoma grade 1 in patients with multiple osteochondromas.
Goud AL; Wuyts W; Bessems J; Bramer J; van der Woude HJ; Ham J
J Bone Joint Surg Am; 2015 Jan; 97(1):24-31. PubMed ID: 25568391
[TBL] [Abstract][Full Text] [Related]
7. Detection of exostosin glycosyltransferase gene mutations in patients with non-hereditary osteochondromas of the mandibular condyle.
Zhou Q; Yang C; Chen MJ; Li LZ
Mol Clin Oncol; 2016 Sep; 5(3):295-299. PubMed ID: 27588195
[TBL] [Abstract][Full Text] [Related]
8. Large-scale mutational analysis in the EXT1 and EXT2 genes for Japanese patients with multiple osteochondromas.
Ishimaru D; Gotoh M; Takayama S; Kosaki R; Matsumoto Y; Narimatsu H; Sato T; Kimata K; Akiyama H; Shimizu K; Matsumoto K
BMC Genet; 2016 Mar; 17():52. PubMed ID: 26961984
[TBL] [Abstract][Full Text] [Related]
9. Targeted Next-Generation Sequencing Newly Identifies Mutations in Exostosin-1 and Exostosin-2 Genes of Patients with Multiple Osteochondromas.
Guo X; Lin M; Shi T; Yan W; Chen W
Tohoku J Exp Med; 2017 Jul; 242(3):173-181. PubMed ID: 28690282
[TBL] [Abstract][Full Text] [Related]
10. Osteochondromas: review of the clinical, radiological and pathological features.
Kitsoulis P; Galani V; Stefanaki K; Paraskevas G; Karatzias G; Agnantis NJ; Bai M
In Vivo; 2008; 22(5):633-46. PubMed ID: 18853760
[TBL] [Abstract][Full Text] [Related]
11. Decreased EXT expression and intracellular accumulation of heparan sulphate proteoglycan in osteochondromas and peripheral chondrosarcomas.
Hameetman L; David G; Yavas A; White SJ; Taminiau AH; Cleton-Jansen AM; Hogendoorn PC; Bovée JV
J Pathol; 2007 Mar; 211(4):399-409. PubMed ID: 17226760
[TBL] [Abstract][Full Text] [Related]
12. Up-regulation of PTHrP and Bcl-2 expression characterizes the progression of osteochondroma towards peripheral chondrosarcoma and is a late event in central chondrosarcoma.
Bovée JV; van den Broek LJ; Cleton-Jansen AM; Hogendoorn PC
Lab Invest; 2000 Dec; 80(12):1925-34. PubMed ID: 11140704
[TBL] [Abstract][Full Text] [Related]
13. HSPG-deficient zebrafish uncovers dental aspect of multiple osteochondromas.
Wiweger MI; Zhao Z; van Merkesteyn RJ; Roehl HH; Hogendoorn PC
PLoS One; 2012; 7(1):e29734. PubMed ID: 22253766
[TBL] [Abstract][Full Text] [Related]
14. Phenotypic and Molecular Spectrum of a Turkish Cohort with Hereditary Multiple Osteochondromas.
Güneş N; Uludağ Alkaya D; Toylu A; Özüdoğru P; Çifçi Sunamak E; Şeker A; Demir B; Kuruğoğlu S; Mıhçı E; Tüysüz B
Turk Arch Pediatr; 2023 Jul; 58(4):376-381. PubMed ID: 37317574
[TBL] [Abstract][Full Text] [Related]
15. Mutation screening for the EXT1 and EXT2 genes in Chinese patients with multiple osteochondromas.
Kang QL; Xu J; Zhang Z; He JW; Fu WZ; Zhang ZL
Arch Med Res; 2013 Oct; 44(7):542-8. PubMed ID: 24120389
[TBL] [Abstract][Full Text] [Related]
16. Identification of a novel frameshift mutation of the
Xia P; Xu H; Shi Q; Li D
Oncol Lett; 2016 Jan; 11(1):105-110. PubMed ID: 26870176
[TBL] [Abstract][Full Text] [Related]
17. An update on the imaging of diaphyseal aclasis.
Ellatif M; Sharif B; Lindsay D; Pollock R; Saifuddin A
Skeletal Radiol; 2021 Oct; 50(10):1941-1962. PubMed ID: 33791832
[TBL] [Abstract][Full Text] [Related]
18. Identification of a rare case of intra-articular osteochondroma manifesting as three loose bodies in a patient with hereditary multiple osteochondromas: A case report.
Kong M; Cao LI; Zhang Q; Fang Y; Zhao C; Gu H; Zhang S; Chen YU; Wu J; Bi Q
Oncol Lett; 2015 Aug; 10(2):798-804. PubMed ID: 26622573
[TBL] [Abstract][Full Text] [Related]
19. Hereditary Multiple Exostoses: a review of clinical appearance and metabolic pattern.
Beltrami G; Ristori G; Scoccianti G; Tamburini A; Capanna R
Clin Cases Miner Bone Metab; 2016; 13(2):110-118. PubMed ID: 27920806
[TBL] [Abstract][Full Text] [Related]
20. Peripheral chondrosarcoma progression is associated with increased type X collagen and vascularisation.
de Andrea CE; Wiweger MI; Bovée JV; Romeo S; Hogendoorn PC
Virchows Arch; 2012 Jan; 460(1):95-102. PubMed ID: 22116208
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]