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Journal Abstract Search

297 related items for PubMed ID: 35000307

  • 1. [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
    [Abstract] [Full Text] [Related]

  • 2. Birt-Hogg-Dubé syndrome: a large single family cohort.
    Skolnik K, Tsai WH, Dornan K, Perrier R, Burrowes PW, Davidson WJ.
    Respir Res; 2016 Feb 29; 17():22. PubMed ID: 26928018
    [Abstract] [Full Text] [Related]

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

  • 4. Birt-Hogg-Dubé syndrome in Korean: clinicoradiologic features and long term follow-up.
    Lee JH, Jeon MJ, Song JS, Chae EJ, Choi JH, Kim GH, Song JW.
    Korean J Intern Med; 2019 Jul 19; 34(4):830-840. PubMed ID: 30360018
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

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

  • 7. 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 Jan 09; 98(2):125-132. PubMed ID: 31266032
    [Abstract] [Full Text] [Related]

  • 8. Delayed diagnosis of Birt-Hogg-Dubé syndrome due to marked intrafamilial clinical variability: a case report.
    Sattler EC, Steinlein OK.
    BMC Med Genet; 2018 Mar 16; 19(1):45. PubMed ID: 29548312
    [Abstract] [Full Text] [Related]

  • 9. Birt-Hogg-Dubé syndrome in a patient presenting with familial spontaneous pneumothorax.
    Auerbach A, Roberts DH, Gangadharan SP, Kent MS.
    Ann Thorac Surg; 2014 Jul 16; 98(1):325-7. PubMed ID: 24996715
    [Abstract] [Full Text] [Related]

  • 10. 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 16; 12(2):e0170713. PubMed ID: 28151982
    [Abstract] [Full Text] [Related]

  • 11. Focus on the pulmonary involvement and genetic patterns in Birt-Hogg-Dubè syndrome: Literature review.
    Marziali V, Geropoulos G, Frasca L, Longo F, Patrini D, Panagiotopoulos N, Crucitti P.
    Respir Med; 2020 Jul 16; 168():105995. PubMed ID: 32469710
    [Abstract] [Full Text] [Related]

  • 12. Skin lesions of Birt-Hogg-Dubé syndrome: Clinical and histopathological findings in 31 Japanese patients who presented with pneumothorax and/or multiple lung cysts.
    Iwabuchi C, Ebana H, Ishiko A, Negishi A, Mizobuchi T, Kumasaka T, Kurihara M, Seyama K.
    J Dermatol Sci; 2018 Jan 16; 89(1):77-84. PubMed ID: 29157599
    [Abstract] [Full Text] [Related]

  • 13. 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
    [Abstract] [Full Text] [Related]

  • 14. Partial pleural covering for intractable pneumothorax in patients with Birt-Hogg-Dubé Syndrome.
    Okada A, Hirono T, Watanabe T, Hasegawa G, Tanaka R, Furuya M.
    Clin Respir J; 2017 Mar 06; 11(2):224-229. PubMed ID: 26073198
    [Abstract] [Full Text] [Related]

  • 15. Isolated familial pneumothorax in a Taiwanese family with Birt-Hogg-Dubé syndrome.
    Yang CY, Wang HC, Chen JS, Yu CJ.
    J Postgrad Med; 2013 Mar 06; 59(4):321-3. PubMed ID: 24346394
    [Abstract] [Full Text] [Related]

  • 16. A Case of Birt-Hogg-Dubé (BHD) Syndrome Harboring a Novel Folliculin (FLCN) Gene Mutation.
    Yukawa T, Fukazawa T, Yoshida M, Morita I, Kato K, Monobe Y, Furuya M, Naomoto Y.
    Am J Case Rep; 2016 Oct 26; 17():788-792. PubMed ID: 27780965
    [Abstract] [Full Text] [Related]

  • 17. Birt-Hogg-Dubé syndrome in two Chinese families with mutations in the FLCN gene.
    Hou X, Zhou Y, Peng Y, Qiu R, Xia K, Tang B, Zhuang W, Jiang H.
    BMC Med Genet; 2018 Jan 22; 19(1):14. PubMed ID: 29357828
    [Abstract] [Full Text] [Related]

  • 18. Birt-Hogg-Dubé syndrome in Chinese patients: a literature review of 120 families.
    Hu X, Zhang G, Chen X, Xu KF.
    Orphanet J Rare Dis; 2021 May 17; 16(1):223. PubMed ID: 34001170
    [Abstract] [Full Text] [Related]

  • 19. [Expert consensus on the diagnosis and management of Birt-Hogg-Dubé syndrome].
    Expert Consensus Group of the Expert Consensus on the Diagnosis and Management of Birt-Hogg-Dubé Syndrome, China Alliance for the Rare Lung Disease, Chinese Thoracic Society, Chinese Medical Association, Southern China Rare Lung Disease Committee of China Primary Health Care Foundation.
    Zhonghua Jie He He Hu Xi Za Zhi; 2023 Sep 12; 46(9):897-908. PubMed ID: 37670643
    [Abstract] [Full Text] [Related]

  • 20. Spontaneous pneumothorax as indicator for Birt-Hogg-Dubé syndrome in paediatric patients.
    Johannesma PC, van den Borne BE, Gille JJ, Nagelkerke AF, van Waesberghe JT, Paul MA, van Moorselaar RJ, Menko FH, Postmus PE.
    BMC Pediatr; 2014 Jul 03; 14():171. PubMed ID: 24994497
    [Abstract] [Full Text] [Related]

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