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Journal Abstract Search

578 related items for PubMed ID: 29548312

  • 1. 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
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  • 2. 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 16; 21(10):632-634. PubMed ID: 28805452
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  • 3. [Multiple spontaneous pneumothoraces revealing Birt-Hogg-Dube syndrome].
    Van Denhove A, Guillot-Pouget I, Giraud S, Isaac S, Freymond N, Calender A, Pacheco Y, Devouassoux G.
    Rev Mal Respir; 2011 Mar 16; 28(3):355-9. PubMed ID: 21482341
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  • 4. [Are multiple trichodiscomas/fibrofolliculomas the Birt-Hogg-Dubé syndrome?].
    Belousova IE, Shpilyuk RG, Chepushtanova KO, Gorbunov YG, Kazakov DV.
    Arkh Patol; 2021 Mar 16; 83(3):45-51. PubMed ID: 34041896
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  • 6. [Birt-Hogg-Dubé syndrome: an update].
    López V, Jordá E, Monteagudo C.
    Actas Dermosifiliogr; 2012 Apr 16; 103(3):198-206. PubMed ID: 21937013
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  • 9. 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 Apr 16; 98(2):125-132. PubMed ID: 31266032
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  • 13. Birt-Hogg-Dubé syndrome: Clinical and molecular aspects of recently identified kidney cancer syndrome.
    Hasumi H, Baba M, Hasumi Y, Furuya M, Yao M.
    Int J Urol; 2016 Mar 16; 23(3):204-10. PubMed ID: 26608100
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  • 14. Recurrent spontaneous pneumothorax in a patient with Birt-Hogg-Dubé syndrome.
    Predina JD, Kotloff RM, Miller WT, Singhal S.
    Eur J Cardiothorac Surg; 2011 Mar 16; 39(3):404-6. PubMed ID: 20692178
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  • 17. [The Birt-Hogg-Dube Syndrome].
    Schweizer S, Krayenbühl PA.
    Praxis (Bern 1994); 2014 Nov 12; 103(23):1359-66; quiz 1367-8. PubMed ID: 25391741
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  • 19. 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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