227 related articles for article (PubMed ID: 32144835)
1. Natural history of Ollier disease and Maffucci syndrome: Patient survey and review of clinical literature.
El Abiad JM; Robbins SM; Cohen B; Levin AS; Valle DL; Morris CD; de Macena Sobreira NL
Am J Med Genet A; 2020 May; 182(5):1093-1103. PubMed ID: 32144835
[TBL] [Abstract][Full Text] [Related]
2. Skull Base Enchondroma and Chondrosarcoma in Ollier Disease and Maffucci Syndrome.
Oushy S; Peris-Celda M; Van Gompel JJ
World Neurosurg; 2019 Oct; 130():e356-e361. PubMed ID: 31233929
[TBL] [Abstract][Full Text] [Related]
3. Do intracranial neoplasms differ in Ollier disease and maffucci syndrome? An in-depth analysis of the literature.
Ranger A; Szymczak A
Neurosurgery; 2009 Dec; 65(6):1106-13; discussion 1113-5. PubMed ID: 19934970
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Disruption of the HIF-1 pathway in individuals with Ollier disease and Maffucci syndrome.
Poll SR; Martin R; Wohler E; Partan ES; Walek E; Salman S; Groepper D; Kratz L; Cernach M; Jesus-Garcia R; Haldeman-Englert C; Choi YJ; Morris CD; Cohen B; Hoover-Fong J; Valle D; Semenza GL; Sobreira NLM
PLoS Genet; 2022 Dec; 18(12):e1010504. PubMed ID: 36480544
[TBL] [Abstract][Full Text] [Related]
6. Ollier disease.
Silve C; Jüppner H
Orphanet J Rare Dis; 2006 Sep; 1():37. PubMed ID: 16995932
[TBL] [Abstract][Full Text] [Related]
7. Maffucci syndrome: a genome-wide analysis using high resolution single nucleotide polymorphism and expression arrays on four cases.
Pansuriya TC; Oosting J; Verdegaal SH; Flanagan AM; Sciot R; Kindblom LG; Hogendoorn PC; Szuhai K; Bovée JV
Genes Chromosomes Cancer; 2011 Sep; 50(9):673-9. PubMed ID: 21584901
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Incidence, predictive factors, and prognosis of chondrosarcoma in patients with Ollier disease and Maffucci syndrome: an international multicenter study of 161 patients.
Verdegaal SH; Bovée JV; Pansuriya TC; Grimer RJ; Ozger H; Jutte PC; San Julian M; Biau DJ; van der Geest IC; Leithner A; Streitbürger A; Klenke FM; Gouin FG; Campanacci DA; Marec-Berard P; Hogendoorn PC; Brand R; Taminiau AH
Oncologist; 2011; 16(12):1771-9. PubMed ID: 22147000
[TBL] [Abstract][Full Text] [Related]
10. Maffucci syndrome complicated by three different central nervous system tumors sharing an IDH1 R132C mutation: case report.
Nejo T; Tanaka S; Ikemura M; Nomura M; Takayanagi S; Shin M; Ushiku T; Shibahara J; Saito N; Mukasa A
J Neurosurg; 2018 Dec; 131(6):1829-1834. PubMed ID: 30579273
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. First case of juvenile granulosa cell tumor in an adult with Ollier disease.
Rietveld L; Nieboer TE; Kluivers KB; Schreuder HW; Bulten J; Massuger LF
Int J Gynecol Pathol; 2009 Sep; 28(5):464-7. PubMed ID: 19696617
[TBL] [Abstract][Full Text] [Related]
13. cDNA expression profiling of chondrosarcomas: Ollier disease resembles solitary tumours and alteration in genes coding for components of energy metabolism occurs with increasing grade.
Rozeman LB; Hameetman L; van Wezel T; Taminiau AH; Cleton-Jansen AM; Hogendoorn PC; Bovée JV
J Pathol; 2005 Sep; 207(1):61-71. PubMed ID: 16007578
[TBL] [Abstract][Full Text] [Related]
14. Skull Base Chondrosarcoma Caused by Ollier Disease: A Case Report and Literature Review.
Ding C; Chen W; Liu F; Xiong M; Chen J
World Neurosurg; 2019 Jul; 127():103-108. PubMed ID: 30872199
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Common somatic alterations identified in maffucci syndrome by molecular karyotyping.
Amyere M; Dompmartin A; Wouters V; Enjolras O; Kaitila I; Docquier PL; Godfraind C; Mulliken JB; Boon LM; Vikkula M
Mol Syndromol; 2014 Dec; 5(6):259-67. PubMed ID: 25565925
[TBL] [Abstract][Full Text] [Related]
17. Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome.
Pansuriya TC; van Eijk R; d'Adamo P; van Ruler MA; Kuijjer ML; Oosting J; Cleton-Jansen AM; van Oosterwijk JG; Verbeke SL; Meijer D; van Wezel T; Nord KH; Sangiorgi L; Toker B; Liegl-Atzwanger B; San-Julian M; Sciot R; Limaye N; Kindblom LG; Daugaard S; Godfraind C; Boon LM; Vikkula M; Kurek KC; Szuhai K; French PJ; Bovée JV
Nat Genet; 2011 Nov; 43(12):1256-61. PubMed ID: 22057234
[TBL] [Abstract][Full Text] [Related]
18. The malignant potential of enchondromatosis.
Schwartz HS; Zimmerman NB; Simon MA; Wroble RR; Millar EA; Bonfiglio M
J Bone Joint Surg Am; 1987 Feb; 69(2):269-74. PubMed ID: 3805090
[TBL] [Abstract][Full Text] [Related]
19. Hand involvement in Ollier Disease and Maffucci Syndrome: a case series.
Casal D; Mavioso C; Mendes MM; Mouzinho MM
Acta Reumatol Port; 2010; 35(3):375-8. PubMed ID: 20975644
[TBL] [Abstract][Full Text] [Related]
20. Enchondromatosis: insights on the different subtypes.
Pansuriya TC; Kroon HM; Bovée JV
Int J Clin Exp Pathol; 2010 Jun; 3(6):557-69. PubMed ID: 20661403
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
