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PUBMED FOR HANDHELDS

Journal Abstract Search


242 related items for PubMed ID: 27734835

  • 21.
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  • 22. Birt-Hogg-Dubé syndrome: from gene discovery to molecularly targeted therapies.
    Schmidt LS.
    Fam Cancer; 2013 Sep; 12(3):357-64. PubMed ID: 23108783
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  • 23. Focus on the pulmonary involvement and genetic patterns in Birt-Hogg-Dubè syndrome: Literature review.
    Marziali V, Geropoulos G, Frasca L, Longo F, Patrini D, Panagiotopoulos N, Crucitti P.
    Respir Med; 2020 Jul; 168():105995. PubMed ID: 32469710
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  • 26. Are lung cysts in renal cell cancer (RCC) patients an indication for FLCN mutation analysis?
    Johannesma PC, Houweling AC, Menko FH, van de Beek I, Reinhard R, Gille JJ, van Waesberghe JT, Thunnissen E, Starink TM, Postmus PE, van Moorselaar RJ.
    Fam Cancer; 2016 Apr; 15(2):297-300. PubMed ID: 26603437
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  • 27. Investigation of the Birt-Hogg-Dube tumour suppressor gene (FLCN) in familial and sporadic colorectal cancer.
    Nahorski MS, Lim DH, Martin L, Gille JJ, McKay K, Rehal PK, Ploeger HM, van Steensel M, Tomlinson IP, Latif F, Menko FH, Maher ER.
    J Med Genet; 2010 Jun; 47(6):385-90. PubMed ID: 20522427
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  • 30. 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; 79(4):345-54. PubMed ID: 20618353
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  • 31.
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  • 32. FLCN: The causative gene for Birt-Hogg-Dubé syndrome.
    Schmidt LS, Linehan WM.
    Gene; 2018 Jan 15; 640():28-42. PubMed ID: 28970150
    [Abstract] [Full Text] [Related]

  • 33. 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 15; 23(3):204-10. PubMed ID: 26608100
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  • 35. Birt-Hogg-Dubé syndrome: an underdiagnosed genetic tumor syndrome.
    Steinlein OK, Ertl-Wagner B, Ruzicka T, Sattler EC.
    J Dtsch Dermatol Ges; 2018 Mar 15; 16(3):278-283. PubMed ID: 29537177
    [Abstract] [Full Text] [Related]

  • 36. A splicing mutation of the FLCN gene is associated with Birt-Hogg-Dubé syndrome characterized by familial and recurrent spontaneous pneumothorax: A case report.
    Xiao H, Chi F, Li S, Wang T, Bai B, Hou J, Ge X.
    Medicine (Baltimore); 2023 Jul 07; 102(27):e34241. PubMed ID: 37417625
    [Abstract] [Full Text] [Related]

  • 37. 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 07; 50(6):466-77. PubMed ID: 21412933
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  • 39. FLCN-Driven Functional Adrenal Cortical Carcinoma with High Mitotic Tumor Grade: Extending the Endocrine Manifestations of Birt-Hogg-Dubé Syndrome.
    Hofstedter R, Sanabria-Salas MC, Di Jiang M, Ezzat S, Mete O, Kim RH.
    Endocr Pathol; 2023 Jun 07; 34(2):257-264. PubMed ID: 36701047
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