BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

148 related articles for article (PubMed ID: 28544751)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 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. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. IDH2 and TP53 mutations are correlated with gliomagenesis in a patient with Maffucci syndrome.
    Moriya K; Kaneko MK; Liu X; Hosaka M; Fujishima F; Sakuma J; Ogasawara S; Watanabe M; Sasahara Y; Kure S; Kato Y
    Cancer Sci; 2014 Mar; 105(3):359-62. PubMed ID: 24344754
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. Isocitrate dehydrogenase 2 mutation is a frequent event in osteosarcoma detected by a multi-specific monoclonal antibody MsMab-1.
    Liu X; Kato Y; Kaneko MK; Sugawara M; Ogasawara S; Tsujimoto Y; Naganuma Y; Yamakawa M; Tsuchiya T; Takagi M
    Cancer Med; 2013 Dec; 2(6):803-14. PubMed ID: 24403254
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Successful treatment of spindle cell hemangiomas in a patient with Maffucci syndrome and review of literatures.
    Lekwuttikarn R; Chang J; Teng JMC
    Dermatol Ther; 2019 May; 32(3):e12919. PubMed ID: 30977938
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.