182 related articles for article (PubMed ID: 26091223)
1. Ollier Disease: Pathogenesis, Diagnosis, and Management.
Kumar A; Jain VK; Bharadwaj M; Arya RK
Orthopedics; 2015 Jun; 38(6):e497-506. PubMed ID: 26091223
[TBL] [Abstract][Full Text] [Related]
2. Ollier disease with digital enchondromatosis: anatomic and functional imaging.
Le BB; Nguyen BD
Clin Nucl Med; 2014 Aug; 39(8):e375-8. PubMed ID: 24152634
[TBL] [Abstract][Full Text] [Related]
3. Clinics in diagnostic imaging (124). Multiple enchondromatosis in Ollier disease.
Khoo RN; Peh WC; Guglielmi G
Singapore Med J; 2008 Oct; 49(10):841-5; quiz 846. PubMed ID: 18946621
[TBL] [Abstract][Full Text] [Related]
4. Ollier disease.
Silve C; Jüppner H
Orphanet J Rare Dis; 2006 Sep; 1():37. PubMed ID: 16995932
[TBL] [Abstract][Full Text] [Related]
5. PTHR1 mutations associated with Ollier disease result in receptor loss of function.
Couvineau A; Wouters V; Bertrand G; Rouyer C; Gérard B; Boon LM; Grandchamp B; Vikkula M; Silve C
Hum Mol Genet; 2008 Sep; 17(18):2766-75. PubMed ID: 18559376
[TBL] [Abstract][Full Text] [Related]
6. Nonoperative Management of Multiple Hand Enchondromas in Ollier Disease With Progressive Ossification.
MacGillis K; King D
Am J Orthop (Belle Mead NJ); 2015 Sep; 44(9):E343-6. PubMed ID: 26372762
[TBL] [Abstract][Full Text] [Related]
7. Update on the imaging features of the enchondromatosis syndromes.
Sharif B; Lindsay D; Saifuddin A
Skeletal Radiol; 2022 Apr; 51(4):747-762. PubMed ID: 34302201
[TBL] [Abstract][Full Text] [Related]
8. Hereditary multiple exostoses and enchondromatosis.
Pannier S; Legeai-Mallet L
Best Pract Res Clin Rheumatol; 2008 Mar; 22(1):45-54. PubMed ID: 18328980
[TBL] [Abstract][Full Text] [Related]
9. Ollier Disease: A Case Series and Literature Review.
Markevičiūtė V; Markevičiūtė MŠ; Stravinskas M
Acta Med Litu; 2021; 28(1):181-188. PubMed ID: 34393643
[TBL] [Abstract][Full Text] [Related]
10. The association of enchondromatosis with malignant transformed chondrosarcoma and ovarian juvenile granulosa cell tumor (Ollier disease).
Burgetova A; Matejovsky Z; Zikan M; Slama J; Dundr P; Skapa P; Benkova K; Cibula D; Fischerova D
Taiwan J Obstet Gynecol; 2017 Apr; 56(2):253-257. PubMed ID: 28420520
[TBL] [Abstract][Full Text] [Related]
11. Juvenile granulosa cell tumor associated with Ollier disease.
Littrell LA; Inwards CY; Hazard FK; Wenger DE
Skeletal Radiol; 2023 Mar; 52(3):605-612. PubMed ID: 35296906
[TBL] [Abstract][Full Text] [Related]
12. [Ollier disease: benign tumours with risk of malignant transformation. A review of 17 cases].
Vázquez-García B; Valverde M; San-Julián M
An Pediatr (Barc); 2011 Mar; 74(3):168-73. PubMed ID: 21237730
[TBL] [Abstract][Full Text] [Related]
13. Genome-wide analysis of Ollier disease: Is it all in the genes?
Pansuriya TC; Oosting J; Krenács T; Taminiau AH; Verdegaal SH; Sangiorgi L; Sciot R; Hogendoorn PC; Szuhai K; Bovée JV
Orphanet J Rare Dis; 2011 Jan; 6():2. PubMed ID: 21235737
[TBL] [Abstract][Full Text] [Related]
14. Ollier Disease: A Case Report and Review of Treatment Options.
Kramer HD; Valentine MJ; Pettinelli N; Kim J; Kramer RC
Cureus; 2023 Aug; 15(8):e43815. PubMed ID: 37731444
[TBL] [Abstract][Full Text] [Related]
15. Ollier disease: two case reports and a review of the literature.
Wang JP; Xu ZY; Bao ZQ; Dai XS; Ma L; Yao N; Wang ZP; Tao YS; Chai DM
Am J Transl Res; 2018; 10(11):3818-3826. PubMed ID: 30662632
[TBL] [Abstract][Full Text] [Related]
16. PET-positive polyostotic fibrous dysplasia mimicking Ollier disease.
Nishio J; Kuwabara Y; Nabeshima S; Iwasaki H; Naito M
In Vivo; 2013; 27(6):821-6. PubMed ID: 24292588
[TBL] [Abstract][Full Text] [Related]
17. Ollier disease with synchronous multicentric chondrosarcomas: scintigraphic and radiologic demonstration.
Nguyen BD
Clin Nucl Med; 2004 Jan; 29(1):45-7. PubMed ID: 14688600
[No Abstract] [Full Text] [Related]
18. Enchondroma of the nasal septum due to Ollier disease: a case report and review of the literature.
Jacobi CM; Hiranya ES; Gay A; Holzmann D; Kollias S; Soyka MB
Head Neck; 2015 Mar; 37(3):E30-3. PubMed ID: 24890303
[TBL] [Abstract][Full Text] [Related]
19. Ollier disease: an interdisciplinary approach.
Little C
Orthop Nurs; 1994; 13(1):50-5. PubMed ID: 8164989
[TBL] [Abstract][Full Text] [Related]
20. Enchondromatosis (Ollier disease, Maffucci syndrome) is not caused by the PTHR1 mutation p.R150C.
Rozeman LB; Sangiorgi L; Briaire-de Bruijn IH; Mainil-Varlet P; Bertoni F; Cleton-Jansen AM; Hogendoorn PC; Bovée JV
Hum Mutat; 2004 Dec; 24(6):466-73. PubMed ID: 15523647
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]