191 related articles for article (PubMed ID: 35765075)
21. 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]
22. 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]
23. Teaching NeuroImage: Histopathologically Confirmed Intracranial Enchondroma/Low-Grade Chondrosarcoma and
Gregory TA; Taylor LP
Neurology; 2021 Oct; 97(17):e1747-e1748. PubMed ID: 34039720
[No Abstract] [Full Text] [Related]
24. A case of Maffucci 's syndrome with pleural effusion: ten-year follow-up.
Biber C; Ergun P; Turay UY; Erdogan Y; Hizel SB
Ann Acad Med Singap; 2004 May; 33(3):347-50. PubMed ID: 15175777
[TBL] [Abstract][Full Text] [Related]
25. Molecular distinction of chondrosarcoma from chondroblastic osteosarcoma through IDH1/2 mutations.
Kerr DA; Lopez HU; Deshpande V; Hornicek FJ; Duan Z; Zhang Y; Rosenberg AE; Borger DR; Nielsen GP
Am J Surg Pathol; 2013 Jun; 37(6):787-95. PubMed ID: 23598960
[TBL] [Abstract][Full Text] [Related]
26. Somatic
Brown NJ; Ye Z; Stutterd C; Jayasinghe SI; Schneider A; Mullen S; Mandelstam SA; Hildebrand MS
Cold Spring Harb Mol Case Stud; 2021 Dec; 7(6):. PubMed ID: 34588213
[TBL] [Abstract][Full Text] [Related]
27. Diagnostic utility of IDH1/2 mutations to distinguish dedifferentiated chondrosarcoma from undifferentiated pleomorphic sarcoma of bone.
Chen S; Fritchie K; Wei S; Ali N; Curless K; Shen T; Brini AT; Latif F; Sumathi V; Siegal GP; Cheng L
Hum Pathol; 2017 Jul; 65():239-246. PubMed ID: 28552826
[TBL] [Abstract][Full Text] [Related]
28. R132C IDH1 mutations are found in spindle cell hemangiomas and not in other vascular tumors or malformations.
Kurek KC; Pansuriya TC; van Ruler MA; van den Akker B; Luks VL; Verbeke SL; Kozakewich HP; Sciot R; Lev D; Lazar AJ; Fletcher CD; Bovée JV
Am J Pathol; 2013 May; 182(5):1494-500. PubMed ID: 23485734
[TBL] [Abstract][Full Text] [Related]
29. Maffucci Syndrome with Intrahepatic Cholangiocarcinoma: A Case Report.
Kobayashi R; Shimizu A; Kubota K; Notake T; Sugenoya S; Hosoda K; Hayashi H; Yasukawa K; Satoh Y; Iwaya M; Sano K; Soejima Y
Case Rep Oncol; 2021; 14(3):1347-1352. PubMed ID: 34720940
[TBL] [Abstract][Full Text] [Related]
30. Cancer surveillance in children with Ollier Disease and Maffucci Syndrome.
Diezi M; Zambelli PY; Superti-Furga A; Unger S; Renella R
Am J Med Genet A; 2021 Apr; 185(4):1338-1340. PubMed ID: 33433055
[No Abstract] [Full Text] [Related]
31. Surgical Management of Multifocal Chondrosarcoma in Ollier Disease.
Kotrych D; Pawlik J; Czajka R; Szczypiór-Piasecka K; Łęgosz P; Bohatyrewicz A; Kołodziej Ł; Ziętek P
Ortop Traumatol Rehabil; 2020 Oct; 22(5):373-383. PubMed ID: 33568569
[TBL] [Abstract][Full Text] [Related]
32. Recurrent chondrosarcoma of the right skull base in a patient with Maffucci syndrome.
Abdelmalek M; Stanko C
Am J Clin Dermatol; 2008; 9(1):61-5. PubMed ID: 18092846
[TBL] [Abstract][Full Text] [Related]
33. Tracheal chondrosarcoma--a rare complication in Maffucci syndrome.
Wagnetz U; Patsios D; Darling G; Las Heras F; Hwang D
Br J Radiol; 2009 Aug; 82(981):e178-81. PubMed ID: 19729547
[TBL] [Abstract][Full Text] [Related]
34. Case report 492: Chondrosarcoma of right ischium developing in a patient with Maffucci syndrome.
Howie FM; Davidson JK
Skeletal Radiol; 1988; 17(5):368-74. PubMed ID: 3175698
[No Abstract] [Full Text] [Related]
35. 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]
36. Prognostic importance of IDH mutations in chondrosarcoma: An individual patient data meta-analysis.
Vuong HG; Ngo TNM; Dunn IF
Cancer Med; 2021 Jul; 10(13):4415-4423. PubMed ID: 34085407
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. IDH1 Mutation Induces HIF-1
Hu X; Li L; Eid JE; Liu C; Yu J; Yue J; Trent JC
Dis Markers; 2022; 2022():7729968. PubMed ID: 35198082
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. 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]
[Previous] [Next] [New Search]
