278 related articles for article (PubMed ID: 27486260)
21. 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; 17(1):43. PubMed ID: 28222720
[TBL] [Abstract][Full Text] [Related]
22. 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; 105(12):1912-9. PubMed ID: 22146830
[TBL] [Abstract][Full Text] [Related]
23. Isolated familial pneumothorax in a Taiwanese family with Birt-Hogg-Dubé syndrome.
Yang CY; Wang HC; Chen JS; Yu CJ
J Postgrad Med; 2013; 59(4):321-3. PubMed ID: 24346394
[TBL] [Abstract][Full Text] [Related]
24. 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
[TBL] [Abstract][Full Text] [Related]
25. A rapid NGS strategy for comprehensive molecular diagnosis of Birt-Hogg-Dubé syndrome in patients with primary spontaneous pneumothorax.
Zhang X; Ma D; Zou W; Ding Y; Zhu C; Min H; Zhang B; Wang W; Chen B; Ye M; Cai M; Pan Y; Cao L; Wan Y; Jin Y; Gao Q; Yi L
Respir Res; 2016 May; 17(1):64. PubMed ID: 27229674
[TBL] [Abstract][Full Text] [Related]
26. 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
[TBL] [Abstract][Full Text] [Related]
27. A vestibular schwannoma in a patient with Birt-Hogg-Dube syndrome.
De Keyzer L; De Leenheer EM; Claes K; Janssens S
Genet Couns; 2014; 25(2):203-8. PubMed ID: 25059020
[TBL] [Abstract][Full Text] [Related]
28. Familial spontaneous pneumothorax.
Chiu HT; Garcia CK
Curr Opin Pulm Med; 2006 Jul; 12(4):268-72. PubMed ID: 16825879
[TBL] [Abstract][Full Text] [Related]
29. 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
[TBL] [Abstract][Full Text] [Related]
30. Detection of
Liu L; Yang K; Wang X; Shi Z; Yang Y; Yuan Y; Guo T; Xiao X; Luo H
Biomed Res Int; 2017; 2017():8751384. PubMed ID: 28785590
[TBL] [Abstract][Full Text] [Related]
31. 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; 12(2):e0170713. PubMed ID: 28151982
[TBL] [Abstract][Full Text] [Related]
32. 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
[TBL] [Abstract][Full Text] [Related]
33. Characterization of a splice-site mutation in the tumor suppressor gene FLCN associated with renal cancer.
Bartram MP; Mishra T; Reintjes N; Fabretti F; Gharbi H; Adam AC; Göbel H; Franke M; Schermer B; Haneder S; Benzing T; Beck BB; Müller RU
BMC Med Genet; 2017 May; 18(1):53. PubMed ID: 28499369
[TBL] [Abstract][Full Text] [Related]
34. 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; 102(27):e34241. PubMed ID: 37417625
[TBL] [Abstract][Full Text] [Related]
35. 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; 50(6):466-77. PubMed ID: 21412933
[TBL] [Abstract][Full Text] [Related]
36. Genetic Risk Factors for Spontaneous Pneumothorax in Birt-Hogg-Dubé Syndrome.
Sattler EC; Syunyaeva Z; Mansmann U; Steinlein OK
Chest; 2020 May; 157(5):1199-1206. PubMed ID: 31958439
[TBL] [Abstract][Full Text] [Related]
37. Exons 1-3 deletion in FLCN is associated with increased risk of pneumothorax in Chinese patients with Birt-Hogg-Dubé syndrome.
Wang Y; Cai M; Jiang X; Lv G; Hu D; Zhang G; Liu J; Wei W; Xiao J; Shen B; Ryu JH; Hu X
Orphanet J Rare Dis; 2023 May; 18(1):115. PubMed ID: 37170274
[TBL] [Abstract][Full Text] [Related]
38. A new locus-specific database (LSDB) for mutations in the folliculin (FLCN) gene.
Lim DH; Rehal PK; Nahorski MS; Macdonald F; Claessens T; Van Geel M; Gijezen L; Gille JJ; Giraud S; Richard S; van Steensel M; Menko FH; Maher ER
Hum Mutat; 2010 Jan; 31(1):E1043-51. PubMed ID: 19802896
[TBL] [Abstract][Full Text] [Related]
39. Identification of a Novel Pathogenic Folliculin Variant in a Chinese Family With Birt-Hogg-Dubé Syndrome (Hornstein-Knickenberg Syndrome).
Zong D; Li J; Liu X; Guo T; Ouyang R
Front Genet; 2020; 11():565566. PubMed ID: 33240319
[TBL] [Abstract][Full Text] [Related]
40. Delayed diagnosis of Birt-Hogg-Dubé syndrome due to marked intrafamilial clinical variability: a case report.
Sattler EC; Steinlein OK
BMC Med Genet; 2018 Mar; 19(1):45. PubMed ID: 29548312
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
