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Journal Abstract Search

173 related items for PubMed ID: 25059020

  • 1. A vestibular schwannoma in a patient with Birt-Hogg-Dube syndrome.
    De Keyzer L, De Leenheer EM, Claes K, Janssens S.
    Genet Couns; 2014; 25(2):203-8. PubMed ID: 25059020
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  • 4. 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; 4(21):. PubMed ID: 27905298
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  • 5. 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; 23(3):204-10. PubMed ID: 26608100
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  • 6. 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
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  • 7. Identification of intragenic deletions and duplication in the FLCN gene in Birt-Hogg-Dubé syndrome.
    Benhammou JN, Vocke CD, Santani A, Schmidt LS, Baba M, Seyama K, Wu X, Korolevich S, Nathanson KL, Stolle CA, Linehan WM.
    Genes Chromosomes Cancer; 2011 Jun 21; 50(6):466-77. PubMed ID: 21412933
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  • 8. Birt-Hogg-Dubé syndrome with a renal angiomyolipoma: further evidence of a relationship between Birt-Hogg-Dubé syndrome and tuberous sclerosis complex.
    Byrne M, Mallipeddi R, Pichert G, Whittaker S.
    Australas J Dermatol; 2012 May 21; 53(2):151-4. PubMed ID: 22571569
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  • 9. Birt-Hogg-Dubé syndrome: report of a new mutation.
    Rehman HU.
    Can Respir J; 2012 May 21; 19(3):193-5. PubMed ID: 22679611
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  • 10. Birt-Hogg-Dubé renal tumors are genetically distinct from other renal neoplasias and are associated with up-regulation of mitochondrial gene expression.
    Klomp JA, Petillo D, Niemi NM, Dykema KJ, Chen J, Yang XJ, Sääf A, Zickert P, Aly M, Bergerheim U, Nordenskjöld M, Gad S, Giraud S, Denoux Y, Yonneau L, Méjean A, Vasiliu V, Richard S, MacKeigan JP, Teh BT, Furge KA.
    BMC Med Genomics; 2010 Dec 16; 3():59. PubMed ID: 21162720
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  • 11. [Birt-Hogg-Dubé syndrome].
    Křepelová A, Puchmajerová A, Vasovčák P, Chocholatý M.
    Klin Onkol; 2012 Dec 16; 25 Suppl():S18-20. PubMed ID: 22920201
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  • 13. 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 Dec 16; 98(2):125-132. PubMed ID: 31266032
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  • 15. Lymphoplasmacytic lymphoma in a patient with Birt-Hogg-Dubé syndrome.
    Kurata K, Matsumoto H, Jimbo N, Yakushijin K, Yamamoto K, Ito M, Nakamachi Y, Matsuoka H, Saegusa J, Seyama K, Itoh T, Minami H.
    Int J Hematol; 2020 Dec 16; 112(6):864-870. PubMed ID: 32789566
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  • 16. Novel folliculin (FLCN) mutation and familial spontaneous pneumothorax.
    Zhu JF, Shen XQ, Zhu F, Tian L.
    QJM; 2017 Jan 16; 110(1):23-26. PubMed ID: 27486260
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  • 17. Constitutional FLCN mutations in patients with suspected Birt-Hogg-Dubé syndrome ascertained for non-cutaneous manifestations.
    Maffé A, Toschi B, Circo G, Giachino D, Giglio S, Rizzo A, Carloni A, Poletti V, Tomassetti S, Ginardi C, Ungari S, Genuardi M.
    Clin Genet; 2011 Apr 16; 79(4):345-54. PubMed ID: 20618353
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  • 18. 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
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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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