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Journal Abstract Search

209 related items for PubMed ID: 25827758

  • 1. Genetic analysis of familial spontaneous pneumothorax in an Indian family.
    Ray A, Paul S, Chattopadhyay E, Kundu S, Roy B.
    Lung; 2015 Jun; 193(3):433-8. PubMed ID: 25827758
    [Abstract] [Full Text] [Related]

  • 2. Novel folliculin (FLCN) mutation and familial spontaneous pneumothorax.
    Zhu JF, Shen XQ, Zhu F, Tian L.
    QJM; 2017 Jan; 110(1):23-26. PubMed ID: 27486260
    [Abstract] [Full Text] [Related]

  • 3. 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; 98(2):125-132. PubMed ID: 31266032
    [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; 34(4):830-840. PubMed ID: 30360018
    [Abstract] [Full Text] [Related]

  • 5. Birt-Hogg-Dube Syndrome with a Novel Mutation in the FLCN Gene.
    Kayhan G, Yılmaz Demirci N, Turktas H, Ergun MA.
    Genet Test Mol Biomarkers; 2017 Oct; 21(10):632-634. PubMed ID: 28805452
    [Abstract] [Full Text] [Related]

  • 6. Birt-Hogg-Dubé syndrome. State-of-the-art review with emphasis on pulmonary involvement.
    Dal Sasso AA, Belém LC, Zanetti G, Souza CA, Escuissato DL, Irion KL, Guimarães MD, Marchiori E.
    Respir Med; 2015 Mar; 109(3):289-96. PubMed ID: 25519092
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. 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 22; 89(1):77-84. PubMed ID: 29157599
    [Abstract] [Full Text] [Related]

  • 9. Genotypic characteristics of Chinese patients with BHD syndrome and functional analysis of FLCN variants.
    Liu K, Xu W, Tian X, Xiao M, Zhao X, Zhang Q, Qu T, Song J, Liu Y, Xu KF, Zhang X.
    Orphanet J Rare Dis; 2019 Oct 15; 14(1):223. PubMed ID: 31615547
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. Recurrent primary spontaneous pneumothorax in a large Chinese family: a clinical and genetic investigation.
    Zheng CM, Hu XX, Gao YL, Miao JB, Li H.
    Chin Med J (Engl); 2019 Oct 20; 132(20):2402-2407. PubMed ID: 31567476
    [Abstract] [Full Text] [Related]

  • 12. 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 20; 98(1):325-7. PubMed ID: 24996715
    [Abstract] [Full Text] [Related]

  • 13. Benign clear cell "sugar" tumor of the lung in a patient with Birt-Hogg-Dubé syndrome: a case report.
    Gunji-Niitsu Y, Kumasaka T, Kitamura S, Hoshika Y, Hayashi T, Tokuda H, Morita R, Kobayashi E, Mitani K, Kikkawa M, Takahashi K, Seyama K.
    BMC Med Genet; 2016 Nov 21; 17(1):85. PubMed ID: 27871249
    [Abstract] [Full Text] [Related]

  • 14. Haploinsufficiency of the folliculin gene leads to impaired functions of lung fibroblasts in patients with Birt-Hogg-Dubé syndrome.
    Hoshika Y, Takahashi F, Togo S, Hashimoto M, Nara T, Kobayashi T, Nurwidya F, Kataoka H, Kurihara M, Kobayashi E, Ebana H, Kikkawa M, Ando K, Nishino K, Hino O, Takahashi K, Seyama K.
    Physiol Rep; 2016 Nov 21; 4(21):. PubMed ID: 27905298
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. Isolated familial pneumothorax in a Taiwanese family with Birt-Hogg-Dubé syndrome.
    Yang CY, Wang HC, Chen JS, Yu CJ.
    J Postgrad Med; 2013 Oct 26; 59(4):321-3. PubMed ID: 24346394
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. A rapid NGS strategy for comprehensive molecular diagnosis of Birt-Hogg-Dubé syndrome in patients with primary spontaneous pneumothorax.
    Zhang X, Ma D, Zou W, Ding Y, Zhu C, Min H, Zhang B, Wang W, Chen B, Ye M, Cai M, Pan Y, Cao L, Wan Y, Jin Y, Gao Q, Yi L.
    Respir Res; 2016 May 27; 17(1):64. PubMed ID: 27229674
    [Abstract] [Full Text] [Related]

  • 19. Birt-Hogg-Dubé syndrome: clinical and genetic studies of 10 French families.
    Kluger N, Giraud S, Coupier I, Avril MF, Dereure O, Guillot B, Richard S, Bessis D.
    Br J Dermatol; 2010 Mar 27; 162(3):527-37. PubMed ID: 19785621
    [Abstract] [Full Text] [Related]

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