508 related articles for article (PubMed ID: 21794948)
21. Case Report of Birt-Hogg-Dubé Syndrome: Germline Mutations of FLCN Detected in Patients With Renal Cancer and Thyroid Cancer.
Dong L; Gao M; Hao WJ; Zheng XQ; Li YG; Li XL; Yu Y
Medicine (Baltimore); 2016 May; 95(22):e3695. PubMed ID: 27258496
[TBL] [Abstract][Full Text] [Related]
22. 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; 63(1):45-55. PubMed ID: 23356225
[TBL] [Abstract][Full Text] [Related]
23. [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; 28(3):355-9. PubMed ID: 21482341
[TBL] [Abstract][Full Text] [Related]
24. [Birt-Hogg-Dubé syndrome: an update].
López V; Jordá E; Monteagudo C
Actas Dermosifiliogr; 2012 Apr; 103(3):198-206. PubMed ID: 21937013
[TBL] [Abstract][Full Text] [Related]
25. Syndrome of Birt-Hogg-Dubé, a histopathological pitfall with similarities to tuberous sclerosis: a report of three cases.
Spring P; Fellmann F; Giraud S; Clayton H; Hohl D
Am J Dermatopathol; 2013 Apr; 35(2):241-5. PubMed ID: 23542717
[TBL] [Abstract][Full Text] [Related]
26. 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; 15(1):127-32. PubMed ID: 26342594
[TBL] [Abstract][Full Text] [Related]
27. 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; 17():788-792. PubMed ID: 27780965
[TBL] [Abstract][Full Text] [Related]
28. 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; 19(1):14. PubMed ID: 29357828
[TBL] [Abstract][Full Text] [Related]
29. 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; 17(1):85. PubMed ID: 27871249
[TBL] [Abstract][Full Text] [Related]
30. 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; 90(5):403-412. PubMed ID: 27220747
[TBL] [Abstract][Full Text] [Related]
31. Novel intronic germline FLCN gene mutation in a patient with multiple ipsilateral renal neoplasms.
Gatalica Z; Lilleberg SL; Vranic S; Eyzaguirre E; Orihuela E; Velagaleti G
Hum Pathol; 2009 Dec; 40(12):1813-9. PubMed ID: 19733897
[TBL] [Abstract][Full Text] [Related]
32. [Spontaneous pneumothorax as the first manifestation of a hereditary condition with an increased renal cancer risk].
Johannesma PC; Lammers JW; van Moorselaar RJ; Starink TM; Postmus PE; Menko FH
Ned Tijdschr Geneeskd; 2009; 153():A581. PubMed ID: 19857281
[TBL] [Abstract][Full Text] [Related]
33. Hereditary multiple fibrofolliculomas, trichodiscomas and acrochordons: syndrome of Birt-Hogg-Dubè.
Scalvenzi M; Argenziano G; Sammarco E; Delfino M
J Eur Acad Dermatol Venereol; 1998 Jul; 11(1):45-7. PubMed ID: 9731965
[TBL] [Abstract][Full Text] [Related]
34. 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; 19(1):87-101. PubMed ID: 28695430
[TBL] [Abstract][Full Text] [Related]
35. 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; 69(1):1-12. PubMed ID: 30632664
[TBL] [Abstract][Full Text] [Related]
36. Birt Hogg-Dubé syndrome-associated FLCN mutations disrupt protein stability.
Nahorski MS; Reiman A; Lim DH; Nookala RK; Seabra L; Lu X; Fenton J; Boora U; Nordenskjöld M; Latif F; Hurst LD; Maher ER
Hum Mutat; 2011 Aug; 32(8):921-9. PubMed ID: 21538689
[TBL] [Abstract][Full Text] [Related]
37. 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; 36(4):589-600. PubMed ID: 22441547
[TBL] [Abstract][Full Text] [Related]
38. Nonsense mutations in folliculin presenting as isolated familial spontaneous pneumothorax in adults.
Graham RB; Nolasco M; Peterlin B; Garcia CK
Am J Respir Crit Care Med; 2005 Jul; 172(1):39-44. PubMed ID: 15805188
[TBL] [Abstract][Full Text] [Related]
39. 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; 14(1):223. PubMed ID: 31615547
[TBL] [Abstract][Full Text] [Related]
40. 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; 14():171. PubMed ID: 24994497
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]