156 related articles for article (PubMed ID: 26622573)
1. 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]
2. 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]
3. 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]
4. Intra-articular osteochondroma of the knee joint in a patient with hereditary multiple osteochondromatosis.
Matsumoto Y; Matsuda S; Matono K; Oda Y; Tsuneyoshi M; Iwamoto Y
Fukuoka Igaku Zasshi; 2007 Dec; 98(12):425-30. PubMed ID: 18260368
[TBL] [Abstract][Full Text] [Related]
5. Arthroscopic resection of extra-articular knee osteochondroma: report of two cases.
Tsakotos G; Tokis A; Vlasis K; Demesticha T; Skandalakis P; Filippou D; Piagkou M
J Surg Case Rep; 2019 Jun; 2019(6):rjz167. PubMed ID: 31214309
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Genetic analysis of seven pateints with Hereditary Multiple Osteochondromas (HMO).
Ren Z; Yuan JY; Zhang J; Tan Y; Chen WQ; Zhang ZT; Li YZ
Am J Transl Res; 2022; 14(9):6303-6312. PubMed ID: 36247276
[TBL] [Abstract][Full Text] [Related]
8. Hereditary multiple osteochondromas in Jordanian patients: Mutational and immunohistochemical analysis of
Mohaidat Z; Bodoor K; Almomani R; Alorjani M; Awwad MA; Bany-Khalaf A; Al-Batayneh K
Oncol Lett; 2021 Feb; 21(2):151. PubMed ID: 33552269
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Multiple osteochondromas: mutation update and description of the multiple osteochondromas mutation database (MOdb).
Jennes I; Pedrini E; Zuntini M; Mordenti M; Balkassmi S; Asteggiano CG; Casey B; Bakker B; Sangiorgi L; Wuyts W
Hum Mutat; 2009 Dec; 30(12):1620-7. PubMed ID: 19810120
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Mutational spectrum and clinical signatures in 114 families with hereditary multiple osteochondromas: insights into molecular properties of selected exostosin variants.
Fusco C; Nardella G; Fischetto R; Copetti M; Petracca A; Annunziata F; Augello B; D'Asdia MC; Petrucci S; Mattina T; Rella A; Cassina M; Bengala M; Biagini T; Causio FA; Caldarini C; Brancati F; De Luca A; Guarnieri V; Micale L; D'Agruma L; Castori M
Hum Mol Genet; 2019 Jul; 28(13):2133-2142. PubMed ID: 30806661
[TBL] [Abstract][Full Text] [Related]
14. Novel exostosin-2 mutation identified in a Chinese family with hereditary multiple osteochondroma.
Ruan W; Cao L; Chen Z; Kong M; Bi Q
Oncol Lett; 2018 Apr; 15(4):4383-4389. PubMed ID: 29541207
[TBL] [Abstract][Full Text] [Related]
15. Identification of Two Novel Frameshift Mutations in Exostosin 1 in Two Families with Multiple Osteochondromas.
Wang CY; Yu F; Jin JY; He JQ; Fan LL; Tang JY; Xiang R
Mol Syndromol; 2021 Apr; 12(2):96-100. PubMed ID: 34012378
[TBL] [Abstract][Full Text] [Related]
16. Dysplasia epiphysealis hemimelica of the knee: an unusual presentation with intra-articular loose bodies and literature review.
Wheeldon G; Altiok H
J Pediatr Orthop B; 2015 Jul; 24(4):326-9. PubMed ID: 25647567
[TBL] [Abstract][Full Text] [Related]
17. Intra-articular loose osteochondroma of the temporomandibular joint.
Graziano P; Spinzia A; Abbate V; Romano A
Int J Oral Maxillofac Surg; 2012 Dec; 41(12):1505-8. PubMed ID: 22464853
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Identification of a new mutation in an Iranian family with hereditary multiple osteochondromas.
Akbaroghli S; Balali M; Kamalidehghan B; Saber S; Aryani O; Meng GY; Houshmand M
Ther Clin Risk Manag; 2017; 13():15-19. PubMed ID: 28053536
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]