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428 related items for PubMed ID: 32469710
1. 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 [Abstract] [Full Text] [Related]
4. 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]
5. Birt-Hogg-Dubé syndrome in Korean: clinicoradiologic features and long term follow-up. Lee JH, Jeon MJ, Song JS, Chae EJ, Choi JH, Kim GH, Song JW. Korean J Intern Med; 2019 Jul; 34(4):830-840. PubMed ID: 30360018 [Abstract] [Full Text] [Related]
6. 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]
8. Birt-Hogg-Dubé Syndrome: A Review of Dermatological Manifestations and Other Symptoms. Tong Y, Schneider JA, Coda AB, Hata TR, Cohen PR. Am J Clin Dermatol; 2018 Feb 21; 19(1):87-101. PubMed ID: 28695430 [Abstract] [Full Text] [Related]
9. Mechanisms of pulmonary cyst pathogenesis in Birt-Hogg-Dube syndrome: The stretch hypothesis. Kennedy JC, Khabibullin D, Henske EP. Semin Cell Dev Biol; 2016 Apr 21; 52():47-52. PubMed ID: 26877139 [Abstract] [Full Text] [Related]
11. Renal cancer and pneumothorax risk in Birt-Hogg-Dubé syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families. Houweling AC, Gijezen LM, Jonker MA, van Doorn MB, Oldenburg RA, van Spaendonck-Zwarts KY, Leter EM, van Os TA, van Grieken NC, Jaspars EH, de Jong MM, Bongers EM, Johannesma PC, Postmus PE, van Moorselaar RJ, van Waesberghe JH, Starink TM, van Steensel MA, Gille JJ, Menko FH. Br J Cancer; 2011 Dec 06; 105(12):1912-9. PubMed ID: 22146830 [Abstract] [Full Text] [Related]
13. 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 06; 149(6):2319-2325. PubMed ID: 36258004 [Abstract] [Full Text] [Related]
14. 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]
15. [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]
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. 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]
18. 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 Feb 29; 98(2):125-132. PubMed ID: 31266032 [Abstract] [Full Text] [Related]
19. 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]
20. Clinical and genetic characteristics of chinese patients with Birt-Hogg-Dubé syndrome. Liu Y, Xu Z, Feng R, Zhan Y, Wang J, Li G, Li X, Zhang W, Hu X, Tian X, Xu KF, Zhang X. Orphanet J Rare Dis; 2017 May 30; 12(1):104. PubMed ID: 28558743 [Abstract] [Full Text] [Related] Page: [Next] [New Search]