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335 related items for PubMed ID: 24994497
1. Spontaneous pneumothorax as indicator for Birt-Hogg-Dubé syndrome in paediatric patients. Johannesma PC, van den Borne BE, Gille JJ, Nagelkerke AF, van Waesberghe JT, Paul MA, van Moorselaar RJ, Menko FH, Postmus PE. BMC Pediatr; 2014 Jul 03; 14():171. PubMed ID: 24994497 [Abstract] [Full Text] [Related]
2. 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]
3. 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 26; 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 26; 11(2):224-229. PubMed ID: 26073198 [Abstract] [Full Text] [Related]
5. 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 Mar 26; 12(2):e0170713. PubMed ID: 28151982 [Abstract] [Full Text] [Related]
6. 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]
7. 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. An 18-year-old man with recurrent pneumothorax since he was 10-year-old. Demir M, Çobanoğlu N. Pediatr Pulmonol; 2016 Dec 21; 51(12):E41-E43. PubMed ID: 27257988 [Abstract] [Full Text] [Related]
12. 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]
14. 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 Jan 09; 98(2):125-132. PubMed ID: 31266032 [Abstract] [Full Text] [Related]
15. 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]
16. 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]
17. 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 29; 34(4):830-840. PubMed ID: 30360018 [Abstract] [Full Text] [Related]
18. Isolated familial pneumothorax in a Taiwanese family with Birt-Hogg-Dubé syndrome. Yang CY, Wang HC, Chen JS, Yu CJ. J Postgrad Med; 2013 Jul 29; 59(4):321-3. PubMed ID: 24346394 [Abstract] [Full Text] [Related]
19. 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 29; 149(6):2319-2325. PubMed ID: 36258004 [Abstract] [Full Text] [Related]
20. 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 29; 15(1):127-32. PubMed ID: 26342594 [Abstract] [Full Text] [Related] Page: [Next] [New Search]