These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 30579273)

  • 1. 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; 2019 Dec; 131(6):1829-1834. PubMed ID: 30579273
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Somatic IDH1 mutation in a pituitary adenoma of a patient with Maffucci syndrome.
    Hao S; Hong CS; Feng J; Yang C; Chittiboina P; Zhang J; Zhuang Z
    J Neurosurg; 2016 Jun; 124(6):1562-7. PubMed ID: 26473790
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Maffucci syndrome complicated by giant chondrosarcoma in the left ankle with an IDH1 R132C mutation: a case report.
    Lv H; Jiang H; Zhang M; Luo H; Hong Z; Yang H; Xu W; Shen B; Zhang W; Qiu H; Zhu R
    World J Surg Oncol; 2022 Jun; 20(1):218. PubMed ID: 35765075
    [TBL] [Abstract][Full Text] [Related]  

  • 4. IDH1 R132C and ERC2 L309I Mutations Contribute to the Development of Maffucci's Syndrome.
    Cheng P; Chen K; Zhang S; Mu KT; Liang S; Zhang Y
    Front Endocrinol (Lausanne); 2021; 12():763349. PubMed ID: 34790172
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Somatic mosaic mutations of IDH1 and NPM1 associated with cup-like acute myeloid leukemia in a patient with Maffucci syndrome.
    Akiyama M; Yamaoka M; Mikami-Terao Y; Ohyama W; Yokoi K; Arakawa Y; Takita J; Suzuki H; Yamada H
    Int J Hematol; 2015 Dec; 102(6):723-8. PubMed ID: 26508204
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A case of Maffucci syndrome with a buccal hemangioma harboring a mutation in IDH1.
    Ichimura N; Yamamoto N; Toyama N; Hibi H
    Oral Oncol; 2021 Nov; 122():105553. PubMed ID: 34624834
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2.
    Amary MF; Damato S; Halai D; Eskandarpour M; Berisha F; Bonar F; McCarthy S; Fantin VR; Straley KS; Lobo S; Aston W; Green CL; Gale RE; Tirabosco R; Futreal A; Campbell P; Presneau N; Flanagan AM
    Nat Genet; 2011 Nov; 43(12):1262-5. PubMed ID: 22057236
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A Rare Co-Occurrence of Maffucci Syndrome and Astrocytoma with IDH1 R132H Mutation: A Case Report.
    Ashirov N; Mammadinova I; Moldabekov A; Zhetpisbaev B; Teltayev D; Ryskeldiyev N; Akshulakov S
    Medicina (Kaunas); 2023 May; 59(6):. PubMed ID: 37374260
    [No Abstract]   [Full Text] [Related]  

  • 10. Clinical and radiological response of Maffucci related enchondromas to mutant IDH1 inhibitor Ivosidenib.
    Funck-Brentano T; Cohen-Solal M; Ducray F; Mandonnet E
    Bone; 2024 Nov; 188():117221. PubMed ID: 39097182
    [TBL] [Abstract][Full Text] [Related]  

  • 11. IDH1 immunohistochemistry reactivity and mosaic IDH1 or IDH2 somatic mutations in pediatric sporadic enchondroma and enchondromatosis.
    Saiji E; Pause FG; Lascombes P; Cerato Biderbost C; Marq NL; Berczy M; Merlini L; Rougemont AL
    Virchows Arch; 2019 Nov; 475(5):625-636. PubMed ID: 31240473
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Supratentorial multifocal gliomas associated with Ollier disease harboring IDH1 R132H mutation: A case report.
    Ikeda H; Yamaguchi S; Ishi Y; Wakabayashi K; Shimizu A; Kanno-Okada H; Endo T; Ota M; Okamoto M; Motegi H; Iwasaki N; Fujimura M
    Neuropathology; 2023 Oct; 43(5):413-420. PubMed ID: 36942363
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Constitutional abnormalities of IDH1 combined with secondary mutations predispose a patient with Maffucci syndrome to acute lymphoblastic leukemia.
    Hirabayashi S; Seki M; Hasegawa D; Kato M; Hyakuna N; Shuo T; Kimura S; Yoshida K; Kataoka K; Fujii Y; Shiraishi Y; Chiba K; Tanaka H; Kiyokawa N; Miyano S; Ogawa S; Takita J; Manabe A
    Pediatr Blood Cancer; 2017 Dec; 64(12):. PubMed ID: 28544751
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Maffucci syndrome and neoplasms: a case report and review of the literature.
    Prokopchuk O; Andres S; Becker K; Holzapfel K; Hartmann D; Friess H
    BMC Res Notes; 2016 Feb; 9():126. PubMed ID: 26920730
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Mutant IDH1 Dysregulates the Differentiation of Mesenchymal Stem Cells in Association with Gene-Specific Histone Modifications to Cartilage- and Bone-Related Genes.
    Jin Y; Elalaf H; Watanabe M; Tamaki S; Hineno S; Matsunaga K; Woltjen K; Kobayashi Y; Nagata S; Ikeya M; Kato T; Okamoto T; Matsuda S; Toguchida J
    PLoS One; 2015; 10(7):e0131998. PubMed ID: 26161668
    [TBL] [Abstract][Full Text] [Related]  

  • 17. IDH1 and IDH2 mutations are frequent events in central chondrosarcoma and central and periosteal chondromas but not in other mesenchymal tumours.
    Amary MF; Bacsi K; Maggiani F; Damato S; Halai D; Berisha F; Pollock R; O'Donnell P; Grigoriadis A; Diss T; Eskandarpour M; Presneau N; Hogendoorn PC; Futreal A; Tirabosco R; Flanagan AM
    J Pathol; 2011 Jul; 224(3):334-43. PubMed ID: 21598255
    [TBL] [Abstract][Full Text] [Related]  

  • 18.
    Chen C; Li J; Jiang T; Tang J; Zhang Z; Luo Y; Wang X; Sun K; Jiang Z; Zhou J; Liu Z
    Diagnostics (Basel); 2022 Nov; 12(11):. PubMed ID: 36428825
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cell-free DNA from plasma as a promising alternative for detection of gene mutations in patients with Maffucci syndrome.
    Sun Y; Fan X; Rao Y; Wang Z; Wang D; Yang X; Zheng L; Wen M; Cai R; Su L
    Hereditas; 2022 Jan; 159(1):4. PubMed ID: 35042566
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.