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Journal Abstract Search

243 related items for PubMed ID: 31177286

  • 1. Familial spontaneous pneumothorax: importance of screening for Birt-Hogg-Dubé syndrome.
    Liu Y, Xing H, Huang Y, Meng S, Wang J.
    Eur J Cardiothorac Surg; 2020 Jan 01; 57(1):39-45. PubMed ID: 31177286
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  • 2. Renal cancer and pneumothorax risk in Birt-Hogg-Dubé syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families.
    Houweling AC, Gijezen LM, Jonker MA, van Doorn MB, Oldenburg RA, van Spaendonck-Zwarts KY, Leter EM, van Os TA, van Grieken NC, Jaspars EH, de Jong MM, Bongers EM, Johannesma PC, Postmus PE, van Moorselaar RJ, van Waesberghe JH, Starink TM, van Steensel MA, Gille JJ, Menko FH.
    Br J Cancer; 2011 Dec 06; 105(12):1912-9. PubMed ID: 22146830
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  • 4. Clinical and genetic characteristics of 100 consecutive patients with Birt-Hogg-Dubé syndrome in Eastern Chinese region.
    Hu D, Wang R, Liu J, Chen X, Jiang X, Xiao J, Ryu JH, Hu X.
    Orphanet J Rare Dis; 2024 Sep 19; 19(1):348. PubMed ID: 39300538
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  • 10. [Two families with Birt-Hogg-Dubé syndrome:case report and literature review].
    Zhan DT, Chen RC, Wang LW.
    Zhonghua Jie He He Hu Xi Za Zhi; 2022 Jan 12; 45(1):59-63. PubMed ID: 35000307
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  • 11. Clinical and genetic study of a large Chinese family presented with familial spontaneous pneumothorax.
    Xing H, Liu Y, Jiang G, Li X, Hou Y, Yang F, Wang J.
    J Thorac Dis; 2017 Jul 12; 9(7):1967-1972. PubMed ID: 28839995
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  • 12. Birt-Hogg-Dube syndrome prospectively detected by review of chest computed tomography scans.
    Park HJ, Park CH, Lee SE, Lee GD, Byun MK, Lee S, Lee KA, Kim TH, Kim SH, Yang SY, Kim HJ, Ahn CM.
    PLoS One; 2017 Jul 12; 12(2):e0170713. PubMed ID: 28151982
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  • 17. Birt-Hogg-Dubé syndrome: a literature review and case study of a Chinese woman presenting a novel FLCN mutation.
    Hao S, Long F, Sun F, Liu T, Li D, Jiang S.
    BMC Pulm Med; 2017 Feb 21; 17(1):43. PubMed ID: 28222720
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  • 18. Familial multiple discoid fibromas: a look-alike of Birt-Hogg-Dubé syndrome not linked to the FLCN locus.
    Starink TM, Houweling AC, van Doorn MB, Leter EM, Jaspars EH, van Moorselaar RJ, Postmus PE, Johannesma PC, van Waesberghe JH, Ploeger MH, Kramer MT, Gille JJ, Waisfisz Q, Menko FH.
    J Am Acad Dermatol; 2012 Feb 21; 66(2):259.e1-9. PubMed ID: 21794948
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  • 19. The Relevance of Family History Taking in the Detection and Management of Birt-Hogg-Dubé Syndrome.
    Torricelli E, Occhipinti M, Cavigli E, Tancredi G, Rosi E, Rossi C, Bonaguro M, Candita L, Papi L, Novelli L, Bezzi M, Bargagli E, Voltolini L, Pistolesi M.
    Respiration; 2019 Feb 21; 98(2):125-132. PubMed ID: 31266032
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  • 20. Novel germline mutations in FLCN gene identified in two Chinese patients with Birt-Hogg-Dubé syndrome.
    Li T, Ning X, He Q, Gong K.
    Chin J Cancer; 2017 Jan 09; 36(1):4. PubMed ID: 28069055
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