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Journal Abstract Search

144 related items for PubMed ID: 27722904

  • 1. Genetically diagnosed Birt-Hogg-Dubé syndrome and familial cerebral cavernous malformations in the same individual: a case report.
    Whitworth J, Stausbøl-Grøn B, Skytte AB.
    Fam Cancer; 2017 Jan; 16(1):139-142. PubMed ID: 27722904
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. 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; 11(2):224-229. PubMed ID: 26073198
    [Abstract] [Full Text] [Related]

  • 4. Distinctive expression patterns of glycoprotein non-metastatic B and folliculin in renal tumors in patients with Birt-Hogg-Dubé syndrome.
    Furuya M, Hong SB, Tanaka R, Kuroda N, Nagashima Y, Nagahama K, Suyama T, Yao M, Nakatani Y.
    Cancer Sci; 2015 Mar; 106(3):315-23. PubMed ID: 25594584
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. Pathology of Birt-Hogg-Dubé syndrome: A special reference of pulmonary manifestations in a Japanese population with a comprehensive analysis and review.
    Furuya M, Nakatani Y.
    Pathol Int; 2019 Jan 26; 69(1):1-12. PubMed ID: 30632664
    [Abstract] [Full Text] [Related]

  • 7. Fluorescent and chromogenic in situ hybridization of CEN17q as a potent useful diagnostic marker for Birt-Hogg-Dubé syndrome-associated chromophobe renal cell carcinomas.
    Kato I, Iribe Y, Nagashima Y, Kuroda N, Tanaka R, Nakatani Y, Hasumi H, Yao M, Furuya M.
    Hum Pathol; 2016 Jun 26; 52():74-82. PubMed ID: 26980015
    [Abstract] [Full Text] [Related]

  • 8. Splice-site mutation causing partial retention of intron in the FLCN gene in Birt-Hogg-Dubé syndrome: a case report.
    Furuya M, Kobayashi H, Baba M, Ito T, Tanaka R, Nakatani Y.
    BMC Med Genomics; 2018 May 02; 11(1):42. PubMed ID: 29720200
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. Birt-Hogg-Dubé syndrome: novel FLCN frameshift deletion in daughter and father with renal cell carcinomas.
    Näf E, Laubscher D, Hopfer H, Streit M, Matyas G.
    Fam Cancer; 2016 Jan 21; 15(1):127-32. PubMed ID: 26342594
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. Birt-Hogg-Dubé syndrome in an African patient and a novel mutation in the FLCN gene.
    Pritchett EN, Kim J, Patel K, Patel T, Cusack CA.
    JAMA Dermatol; 2015 Mar 21; 151(3):348-9. PubMed ID: 25408992
    [No Abstract] [Full Text] [Related]

  • 14. Renal angiomyolipoma in Birt-Hogg-Dube syndrome: A case study supporting overlap with tuberous sclerosis complex.
    Dow E, Winship I.
    Am J Med Genet A; 2016 Dec 21; 170(12):3323-3326. PubMed ID: 27643397
    [Abstract] [Full Text] [Related]

  • 15. Birt-Hogg-Dubé syndrome caused by a mutation of FLCN gene in a CVST patient: a case report.
    Han J, Hao J, Liu R, Xie Y, Kang Z.
    Int J Neurosci; 2020 May 21; 130(5):438-442. PubMed ID: 31694440
    [Abstract] [Full Text] [Related]

  • 16. Syndrome of Birt-Hogg-Dubé, a histopathological pitfall with similarities to tuberous sclerosis: a report of three cases.
    Spring P, Fellmann F, Giraud S, Clayton H, Hohl D.
    Am J Dermatopathol; 2013 Apr 21; 35(2):241-5. PubMed ID: 23542717
    [Abstract] [Full Text] [Related]

  • 17. Pulmonary cysts of Birt-Hogg-Dubé syndrome: a clinicopathologic and immunohistochemical study of 9 families.
    Furuya M, Tanaka R, Koga S, Yatabe Y, Gotoda H, Takagi S, Hsu YH, Fujii T, Okada A, Kuroda N, Moritani S, Mizuno H, Nagashima Y, Nagahama K, Hiroshima K, Yoshino I, Nomura F, Aoki I, Nakatani Y.
    Am J Surg Pathol; 2012 Apr 21; 36(4):589-600. PubMed ID: 22441547
    [Abstract] [Full Text] [Related]

  • 18. 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 Apr 21; 12(2):e0170713. PubMed ID: 28151982
    [Abstract] [Full Text] [Related]

  • 19. 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]

  • 20. Birt-Hogg-Dubé syndrome: report of a new mutation.
    Rehman HU.
    Can Respir J; 2012 Feb 29; 19(3):193-5. PubMed ID: 22679611
    [Abstract] [Full Text] [Related]

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