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Volumn 12, Issue 2, 2007, Pages 308-310

Histological diagnosis of spinal chondrosarcoma by endobronchial ultrasound-guided transbronchial needle aspiration

Author keywords

Bronchoscopy and interventional technique; Molecular biology; Rare lung disease

Indexed keywords

ADULT; ARTICLE; CALCIFICATION; CASE REPORT; CHONDROSARCOMA; COMPUTER ASSISTED TOMOGRAPHY; ECHOGRAPHY; GENETIC ANALYSIS; HEREDITARY MULTIPLE EXOSTOSIS; HUMAN; IMMUNOHISTOCHEMISTRY; MALE; NEEDLE BIOPSY; PRIORITY JOURNAL; SPINE TUMOR;

EID: 33846932744     PISSN: 13237799     EISSN: 14401843     Source Type: Journal    
DOI: 10.1111/j.1440-1843.2006.01028.x     Document Type: Article
Times cited : (19)

References (5)
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    • Real-time endobronchial ultrasound-guided transbronchial needle aspiration of mediastinal and hilar lymph nodes
    • Yasufuku K, Chiyo M, Sekine Y, Chhajed PN, Shibuya K, et al. Real-time endobronchial ultrasound-guided transbronchial needle aspiration of mediastinal and hilar lymph nodes. Chest 2004; 126: 122-8.
    • (2004) Chest , vol.126 , pp. 122-128
    • Yasufuku, K.1    Chiyo, M.2    Sekine, Y.3    Chhajed, P.N.4    Shibuya, K.5
  • 3
    • 33644520895 scopus 로고    scopus 로고
    • Endobronchial ultrasound guided transbronchial needle aspiration for staging of lung cancer
    • Yasufuku K, Chiyo M, Koh E, Moriya Y, Iyoda A, et al. Endobronchial ultrasound guided transbronchial needle aspiration for staging of lung cancer. Lung Cancer 2005; 50: 347-54.
    • (2005) Lung Cancer , vol.50 , pp. 347-354
    • Yasufuku, K.1    Chiyo, M.2    Koh, E.3    Moriya, Y.4    Iyoda, A.5
  • 4
    • 0030891393 scopus 로고    scopus 로고
    • Identification of novel mutations in the human EXT1 tumour suppressor gene
    • Wells DE, Hill A, Lin X, Ahn J, Brown N, et al. Identification of novel mutations in the human EXT1 tumour suppressor gene. Hum. Genet. 1997; 99: 612-5.
    • (1997) Hum. Genet , vol.99 , pp. 612-615
    • Wells, D.E.1    Hill, A.2    Lin, X.3    Ahn, J.4    Brown, N.5
  • 5
    • 0035866027 scopus 로고    scopus 로고
    • Mutation frequencies of EXT1 and EXT2 in 43 Japanese families with hereditary multiple exostoses
    • Seki H, Kubota T, Ikegawa S, Haga N, Fujioka F, et al. Mutation frequencies of EXT1 and EXT2 in 43 Japanese families with hereditary multiple exostoses. Am. J. Med. Genet. 2001; 99: 59-62.
    • (2001) Am. J. Med. Genet , vol.99 , pp. 59-62
    • Seki, H.1    Kubota, T.2    Ikegawa, S.3    Haga, N.4    Fujioka, F.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.