BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

178 related articles for article (PubMed ID: 24432109)

  • 1. Metachondromatosis: more than just multiple osteochondromas.
    Fisher TJ; Williams N; Morris L; Cundy PJ
    J Child Orthop; 2013 Dec; 7(6):455-64. PubMed ID: 24432109
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Chondrosarcoma in Metachondromatosis: A Rare Case Report.
    Jamshidi K; Shooshtarizadeh T; Bahrabadi M
    Acta Med Iran; 2017 Dec; 55(12):793-799. PubMed ID: 29373887
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Exostoses, enchondromatosis and metachondromatosis; diagnosis and management.
    McFarlane J; Knight T; Sinha A; Cole T; Kiely N; Freeman R
    Acta Orthop Belg; 2016 Mar; 82(1):102-5. PubMed ID: 26984661
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Metachondromatosis without Enchondromas: A Case Report and Review of the Literature.
    Kanaya K; Ishikawa A; Yaoita M; Niihori T; Aoki Y; Iba K; Yamashita T
    JBJS Case Connect; 2016; 6(2):e30. PubMed ID: 29252664
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Intraosseous atypical chondroid tumor or chondrosarcoma grade 1 in patients with multiple osteochondromas.
    Goud AL; Wuyts W; Bessems J; Bramer J; van der Woude HJ; Ham J
    J Bone Joint Surg Am; 2015 Jan; 97(1):24-31. PubMed ID: 25568391
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An unusual example of hereditary multiple exostoses: a case report and review of the literature.
    Chilvers R; Gallagher JA; Jeffery N; Bond AP
    BMC Musculoskelet Disord; 2021 Jan; 22(1):96. PubMed ID: 33478453
    [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. Loss-of-function mutations in PTPN11 cause metachondromatosis, but not Ollier disease or Maffucci syndrome.
    Bowen ME; Boyden ED; Holm IA; Campos-Xavier B; Bonafé L; Superti-Furga A; Ikegawa S; Cormier-Daire V; Bovée JV; Pansuriya TC; de Sousa SB; Savarirayan R; Andreucci E; Vikkula M; Garavelli L; Pottinger C; Ogino T; Sakai A; Regazzoni BM; Wuyts W; Sangiorgi L; Pedrini E; Zhu M; Kozakewich HP; Kasser JR; Seidman JG; Kurek KC; Warman ML
    PLoS Genet; 2011 Apr; 7(4):e1002050. PubMed ID: 21533187
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Radiographic evidence of regression of a solitary osteochondroma: a report of 4 cases and a literature review.
    Passanise AM; Mehlman CT; Wall EJ; Dieterle JP
    J Pediatr Orthop; 2011; 31(3):312-6. PubMed ID: 21415692
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Osteochondroma and multiple osteochondromas: recommendations on the diagnostics and follow-up with special consideration to the occurrence of secondary chondrosarcoma].
    Herget GW; Kontny U; Saueressig U; Baumhoer D; Hauschild O; Elger T; Südkamp NP; Uhl M
    Radiologe; 2013 Dec; 53(12):1125-36. PubMed ID: 24129968
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Multiple osteochondromas.
    Bovée JV
    Orphanet J Rare Dis; 2008 Feb; 3():3. PubMed ID: 18271966
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Targeted disruption of Shp2 in chondrocytes leads to metachondromatosis with multiple cartilaginous protrusions.
    Kim HK; Feng GS; Chen D; King PD; Kamiya N
    J Bone Miner Res; 2014 Mar; 29(3):761-9. PubMed ID: 23929766
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. EXT-related pathways are not involved in the pathogenesis of dysplasia epiphysealis hemimelica and metachondromatosis.
    Bovée JV; Hameetman L; Kroon HM; Aigner T; Hogendoorn PC
    J Pathol; 2006 Jul; 209(3):411-9. PubMed ID: 16622899
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A rare association of pathological variant of Alport's syndrome caused by hemizygous 5' splice mutation in intron 10 of COL4A5 gene with metachondromatosis due to heterozygous missense variation in protein tyrosine phosphatase nonreceptor type 11 gene.
    Sethi S; Mehta S; Makkar V; Kaur S; Sohal PM
    Saudi J Kidney Dis Transpl; 2019; 30(4):969-973. PubMed ID: 31464257
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Metachondromatosis.
    Hunter AG; Kozlowski K; Hochberger O
    Can Assoc Radiol J; 1995 Jun; 46(3):202-8. PubMed ID: 7538882
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Clinicopathologic analysis of 154 cases of tumors and tumor-like lesions in the bones of hands and feet].
    Jiang ZM; Zhang HZ; Chen JQ; Liu L
    Zhonghua Bing Li Xue Za Zhi; 2003 Oct; 32(5):417-21. PubMed ID: 14633452
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Metachondromatosis: a report of two cases in a family.
    Ikegawa S; Nagano A; Matsushita T; Nakamura K
    Nihon Seikeigeka Gakkai Zasshi; 1992 May; 66(5):460-6. PubMed ID: 1506743
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Multiple unexpected lesions of metachondromatosis detected by technetium-99m methylene diphosphonate SPECT/CT: A case report.
    Wang Z; Zou Y; Chen Y; Chen Y
    Medicine (Baltimore); 2018 Apr; 97(17):e0512. PubMed ID: 29703018
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.