These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
575 related items for PubMed ID: 27871249
1. 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]
2. Skin lesions of Birt-Hogg-Dubé syndrome: Clinical and histopathological findings in 31 Japanese patients who presented with pneumothorax and/or multiple lung cysts. Iwabuchi C, Ebana H, Ishiko A, Negishi A, Mizobuchi T, Kumasaka T, Kurihara M, Seyama K. J Dermatol Sci; 2018 Jan 21; 89(1):77-84. PubMed ID: 29157599 [Abstract] [Full Text] [Related]
3. 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]
4. 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 [Abstract] [Full Text] [Related]
5. 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 [Abstract] [Full Text] [Related]
6. 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]
7. Genetic, epidemiologic and clinicopathologic studies of Japanese Asian patients with Birt-Hogg-Dubé syndrome. Furuya M, Yao M, Tanaka R, Nagashima Y, Kuroda N, Hasumi H, Baba M, Matsushima J, Nomura F, Nakatani Y. Clin Genet; 2016 Nov 26; 90(5):403-412. PubMed ID: 27220747 [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. 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 [Abstract] [Full Text] [Related]
10. 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 09; 63(4):103820. PubMed ID: 31778855 [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 09; 15(1):127-32. PubMed ID: 26342594 [Abstract] [Full Text] [Related]
12. [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 09; 28(3):355-9. PubMed ID: 21482341 [Abstract] [Full Text] [Related]
13. 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 09; 36(4):589-600. PubMed ID: 22441547 [Abstract] [Full Text] [Related]
14. Heterozygous germline FLCN mutation in Birt-Hogg-Dubé syndrome with bilateral renal hybrid oncocytic/chromophobe tumor and unilateral renal chromophobe cell carcinoma: a case report. Li J, Liu F, Liu X, Hu Y, Liu Z, Shen Y, Wan J. J Cancer Res Clin Oncol; 2023 Jun 09; 149(6):2319-2325. PubMed ID: 36258004 [Abstract] [Full Text] [Related]
15. 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 09; 50(8):968-71. PubMed ID: 21781069 [Abstract] [Full Text] [Related]
16. 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 09; 69(1):1-12. PubMed ID: 30632664 [Abstract] [Full Text] [Related]
17. Establishment and characterization of BHD-F59RSVT, an immortalized cell line derived from a renal cell carcinoma in a patient with Birt-Hogg-Dubé syndrome. Furuya M, Hasumi H, Baba M, Tanaka R, Iribe Y, Onishi T, Nagashima Y, Nakatani Y, Isono Y, Yao M. Lab Invest; 2017 Mar 09; 97(3):343-351. PubMed ID: 27991910 [Abstract] [Full Text] [Related]
18. 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 09; 50(6):466-77. PubMed ID: 21412933 [Abstract] [Full Text] [Related]
19. 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 [Abstract] [Full Text] [Related]
20. 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 22; 4(21):. PubMed ID: 27905298 [Abstract] [Full Text] [Related] Page: [Next] [New Search]