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298 related items for PubMed ID: 23414156

  • 1. Birt-Hogg-Dubé syndrome in a patient with melanoma and a novel mutation in the FCLN gene.
    Mota-Burgos A, Acosta EH, Márquez FV, Mendiola M, Herrera-Ceballos E.
    Int J Dermatol; 2013 Mar; 52(3):323-6. PubMed ID: 23414156
    [Abstract] [Full Text] [Related]

  • 2. Birt-Hogg-Dubé syndrome in a patient with localized fibrofolliculomas and a novel mutation in the FLCN gene.
    Alonso-González J, Rodríguez-Pazos L, Fernández-Redondo V, Vega-Gliemmo A, Toribio J.
    Int J Dermatol; 2011 Aug; 50(8):968-71. PubMed ID: 21781069
    [Abstract] [Full Text] [Related]

  • 3. Choroidal melanoma and lid fibrofoliculomas in Birt-Hogg-Dubé syndrome.
    Fontcuberta IC, Salomão DR, Quiram PA, Pulido JS.
    Ophthalmic Genet; 2011 Sep; 32(3):143-6. PubMed ID: 21401403
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  • 4. 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; 162(3):527-37. PubMed ID: 19785621
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  • 6. Leiomyosarcoma in Birt-Hogg-Dubé Syndrome.
    Bird LM, Kuo DJ, Masser-Frye D, Mo JQ, Elster JD.
    J Pediatr Hematol Oncol; 2020 Mar; 42(2):136-137. PubMed ID: 31929385
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  • 7. Multiple angiomatous nodules: a novel skin tumor in Birt-Hogg-Dubé syndrome.
    Nikolaidou C, Moscarella E, Longo C, Rosato S, Cavazza A, Piana S.
    J Cutan Pathol; 2016 Dec; 43(12):1197-1202. PubMed ID: 27596542
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  • 8. Multiple facial angiofibromas: a cutaneous manifestation of Birt-Hogg-Dubé syndrome.
    Schaffer JV, Gohara MA, McNiff JM, Aasi SZ, Dvoretzky I.
    J Am Acad Dermatol; 2005 Aug; 53(2 Suppl 1):S108-11. PubMed ID: 16021156
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  • 9. A case of Birt-Hogg-Dubé syndrome implying reduced or no wild-type folliculin without mutated protein is pathogenic.
    Enomoto Y, Namba Y, Hoshika Y, Komemushi Y, Mitani K, Kume H, Kobayashi E, Miyama Y, Homma Y, Ushiku T, Seyama K.
    Eur J Med Genet; 2020 Apr; 63(4):103820. PubMed ID: 31778855
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  • 11. Birt-Hogg-Dubé syndrome with simultaneous hyperplastic polyposis of the gastrointestinal tract: case report and review of the literature.
    Balsamo F, Cardoso PAS, do Amaral Junior SA, Theodoro TR, de Sousa Gehrke F, da Silva Pinhal MA, Bianco B, Waisberg J.
    BMC Med Genet; 2020 Mar 14; 21(1):52. PubMed ID: 32171268
    [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
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  • 13. Unique mutation, accelerated mTOR signaling and angiogenesis in the pulmonary cysts of Birt-Hogg-Dubé syndrome.
    Nishii T, Tanabe M, Tanaka R, Matsuzawa T, Okudela K, Nozawa A, Nakatani Y, Furuya M.
    Pathol Int; 2013 Jan 21; 63(1):45-55. PubMed ID: 23356225
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  • 14. 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
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  • 15. 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 15; 66(2):259.e1-9. PubMed ID: 21794948
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  • 16. 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 15; 50(6):466-77. PubMed ID: 21412933
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  • 17. Novel folliculin gene mutations in Polish patients with Birt-Hogg-Dubé syndrome.
    Radzikowska E, Lechowicz U, Winek J, Opoka L.
    Orphanet J Rare Dis; 2021 Jul 06; 16(1):302. PubMed ID: 34229741
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  • 18. FLCN gene-mutated renal cell neoplasms: mother and daughter cases with a novel germline mutation.
    Nagashima Y, Furuya M, Gotohda H, Takagi S, Hes O, Michal M, Grossmann P, Tanaka R, Nakatani Y, Kuroda N.
    Int J Urol; 2012 May 06; 19(5):468-70. PubMed ID: 22211584
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  • 19. 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 06; 53(2):151-4. PubMed ID: 22571569
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  • 20. [Are multiple trichodiscomas/fibrofolliculomas the Birt-Hogg-Dubé syndrome?].
    Belousova IE, Shpilyuk RG, Chepushtanova KO, Gorbunov YG, Kazakov DV.
    Arkh Patol; 2021 May 06; 83(3):45-51. PubMed ID: 34041896
    [Abstract] [Full Text] [Related]

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