175 related articles for article (PubMed ID: 33791832)
1. 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]
2. Sarcomatous transformation in diaphyseal aclasis.
Shah ZK; Peh WC; Wong Y; Shek TW; Davies AM
Australas Radiol; 2007 Apr; 51(2):110-9. PubMed ID: 17419854
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Multimodality imaging features of hereditary multiple exostoses.
Kok HK; Fitzgerald L; Campbell N; Lyburn ID; Munk PL; Buckley O; Torreggiani WC
Br J Radiol; 2013 Oct; 86(1030):20130398. PubMed ID: 24004486
[TBL] [Abstract][Full Text] [Related]
6. Craniomaxillofacial features in hereditary multiple exostosis.
Ruiz LP; Lara JC
J Craniofac Surg; 2012 Jul; 23(4):e336-8. PubMed ID: 22801172
[TBL] [Abstract][Full Text] [Related]
7. An unusual example of hereditary multiple exostoses: a case report and review of the literature.
Chilvers R; Gallagher JA; Jeffery N; Bond AP
BMC Musculoskelet Disord; 2021 Jan; 22(1):96. PubMed ID: 33478453
[TBL] [Abstract][Full Text] [Related]
8. Imaging of osteochondroma: variants and complications with radiologic-pathologic correlation.
Murphey MD; Choi JJ; Kransdorf MJ; Flemming DJ; Gannon FH
Radiographics; 2000; 20(5):1407-34. PubMed ID: 10992031
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Multiple osteochondromas.
Bovée JV
Orphanet J Rare Dis; 2008 Feb; 3():3. PubMed ID: 18271966
[TBL] [Abstract][Full Text] [Related]
11. [Osteochondroma and multiple osteochondromas: recommendations on the diagnostics and follow-up with special consideration to the occurrence of secondary chondrosarcoma].
Herget GW; Kontny U; Saueressig U; Baumhoer D; Hauschild O; Elger T; Südkamp NP; Uhl M
Radiologe; 2013 Dec; 53(12):1125-36. PubMed ID: 24129968
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Multiple hereditary exostoses and enchondromatosis.
Jurik AG
Best Pract Res Clin Rheumatol; 2020 Jun; 34(3):101505. PubMed ID: 32253147
[TBL] [Abstract][Full Text] [Related]
15. Chondrosarcoma in a family with multiple hereditary exostoses.
Kivioja A; Ervasti H; Kinnunen J; Kaitila I; Wolf M; Böhling T
J Bone Joint Surg Br; 2000 Mar; 82(2):261-6. PubMed ID: 10755438
[TBL] [Abstract][Full Text] [Related]
16. Osteochondromas: An Updated Review of Epidemiology, Pathogenesis, Clinical Presentation, Radiological Features and Treatment Options.
Tepelenis K; Papathanakos G; Kitsouli A; Troupis T; Barbouti A; Vlachos K; Kanavaros P; Kitsoulis P
In Vivo; 2021; 35(2):681-691. PubMed ID: 33622860
[TBL] [Abstract][Full Text] [Related]
17. Hereditary Multiple Exostoses-A Review of the Molecular Background, Diagnostics, and Potential Therapeutic Strategies.
Bukowska-Olech E; Trzebiatowska W; Czech W; Drzymała O; Frąk P; Klarowski F; Kłusek P; Szwajkowska A; Jamsheer A
Front Genet; 2021; 12():759129. PubMed ID: 34956317
[TBL] [Abstract][Full Text] [Related]
18. Mutations in the EXT1 and EXT2 genes in hereditary multiple exostoses.
Wuyts W; Van Hul W; De Boulle K; Hendrickx J; Bakker E; Vanhoenacker F; Mollica F; Lüdecke HJ; Sayli BS; Pazzaglia UE; Mortier G; Hamel B; Conrad EU; Matsushita M; Raskind WH; Willems PJ
Am J Hum Genet; 1998 Feb; 62(2):346-54. PubMed ID: 9463333
[TBL] [Abstract][Full Text] [Related]
19. Ext-mutation analysis in Italian sporadic and hereditary osteochondromas.
Gigante M; Matera MG; Seripa D; Izzo AM; Venanzi R; Giannotti A; Digilio MC; Gravina C; Lazzari M; Monteleone G; Monteleone M; Dallapiccola B; Fazio VM
Int J Cancer; 2001 Nov; 95(6):378-83. PubMed ID: 11668521
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]