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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

371 related items for PubMed ID: 18271966

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. [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
    [Abstract] [Full Text] [Related]

  • 4. Similar cytogenetic findings in two synchronous secondary peripheral chondrosarcomas in a patient with multiple osteochondromas.
    Kyriazoglou AI, Dimitriadis E, Arnogiannaki N, Brandal P, Heim S, Pandis N.
    Cancer Genet; 2011 Dec; 204(12):677-81. PubMed ID: 22285020
    [Abstract] [Full Text] [Related]

  • 5. Decreased EXT expression and intracellular accumulation of heparan sulphate proteoglycan in osteochondromas and peripheral chondrosarcomas.
    Hameetman L, David G, Yavas A, White SJ, Taminiau AH, Cleton-Jansen AM, Hogendoorn PC, Bovée JV.
    J Pathol; 2007 Mar; 211(4):399-409. PubMed ID: 17226760
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Hereditary multiple exostoses and enchondromatosis.
    Pannier S, Legeai-Mallet L.
    Best Pract Res Clin Rheumatol; 2008 Mar; 22(1):45-54. PubMed ID: 18328980
    [Abstract] [Full Text] [Related]

  • 9. Somatic loss of an EXT2 gene mutation during malignant progression in a patient with hereditary multiple osteochondromas.
    Musso N, Caronia FP, Castorina S, Lo Monte AI, Barresi V, Condorelli DF.
    Cancer Genet; 2015 Mar; 208(3):62-7. PubMed ID: 25744876
    [Abstract] [Full Text] [Related]

  • 10. Dysplasia epiphysealis hemimelica (Trevor disease): a rare developmental disorder of bone mimicking osteochondroma of long bones.
    Glick R, Khaldi L, Ptaszynski K, Steiner GC.
    Hum Pathol; 2007 Aug; 38(8):1265-72. PubMed ID: 17490719
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. EXT-mutation analysis and loss of heterozygosity in sporadic and hereditary osteochondromas and secondary chondrosarcomas.
    Bovée JV, Cleton-Jansen AM, Wuyts W, Caethoven G, Taminiau AH, Bakker E, Van Hul W, Cornelisse CJ, Hogendoorn PC.
    Am J Hum Genet; 1999 Sep; 65(3):689-98. PubMed ID: 10441575
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Multiple osteochondromas: mutation update and description of the multiple osteochondromas mutation database (MOdb).
    Jennes I, Pedrini E, Zuntini M, Mordenti M, Balkassmi S, Asteggiano CG, Casey B, Bakker B, Sangiorgi L, Wuyts W.
    Hum Mutat; 2009 Dec; 30(12):1620-7. PubMed ID: 19810120
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Signaling systems affecting the severity of multiple osteochondromas.
    Piombo V, Jochmann K, Hoffmann D, Wuelling M, Vortkamp A.
    Bone; 2018 Jun; 111():71-81. PubMed ID: 29545125
    [Abstract] [Full Text] [Related]

  • 17. The neoplastic pathogenesis of solitary and multiple osteochondromas.
    Porter DE, Simpson AH.
    J Pathol; 1999 Jun; 188(2):119-25. PubMed ID: 10398153
    [Abstract] [Full Text] [Related]

  • 18. Is total-body MRI useful as a screening tool to rule out malignant progression in patients with multiple osteochondromas? Results in a single-center cohort of 319 adult patients.
    Van der Woude HJ, Flipsen M, Welsink C, Van der Zwan AL, Ham SJ.
    Skeletal Radiol; 2024 Jan; 53(1):141-150. PubMed ID: 37338590
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 19.