182 related articles for article (PubMed ID: 36599954)
21. Birt-Hogg-Dubé syndrome: clinical and genetic studies of 20 families.
Leter EM; Koopmans AK; Gille JJ; van Os TA; Vittoz GG; David EF; Jaspars EH; Postmus PE; van Moorselaar RJ; Craanen ME; Starink TM; Menko FH
J Invest Dermatol; 2008 Jan; 128(1):45-9. PubMed ID: 17611575
[TBL] [Abstract][Full Text] [Related]
22. 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; 11(1):42. PubMed ID: 29720200
[TBL] [Abstract][Full Text] [Related]
23. Birt-Hogg-Dubé syndrome: an underdiagnosed genetic tumor syndrome.
Steinlein OK; Ertl-Wagner B; Ruzicka T; Sattler EC
J Dtsch Dermatol Ges; 2018 Mar; 16(3):278-283. PubMed ID: 29537177
[TBL] [Abstract][Full Text] [Related]
24. 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; 12(1):104. PubMed ID: 28558743
[TBL] [Abstract][Full Text] [Related]
25. [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]
26. [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]
27. 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; 89(1):77-84. PubMed ID: 29157599
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. BHD-associated kidney cancer exhibits unique molecular characteristics and a wide variety of variants in chromatin remodeling genes.
Hasumi H; Furuya M; Tatsuno K; Yamamoto S; Baba M; Hasumi Y; Isono Y; Suzuki K; Jikuya R; Otake S; Muraoka K; Osaka K; Hayashi N; Makiyama K; Miyoshi Y; Kondo K; Nakaigawa N; Kawahara T; Izumi K; Teranishi J; Yumura Y; Uemura H; Nagashima Y; Metwalli AR; Schmidt LS; Aburatani H; Linehan WM; Yao M
Hum Mol Genet; 2018 Aug; 27(15):2712-2724. PubMed ID: 29767721
[TBL] [Abstract][Full Text] [Related]
30. Nutrient-induced FNIP degradation by SCFβ-TRCP regulates FLCN complex localization and promotes renal cancer progression.
Nagashima K; Fukushima H; Shimizu K; Yamada A; Hidaka M; Hasumi H; Ikebe T; Fukumoto S; Okabe K; Inuzuka H
Oncotarget; 2017 Feb; 8(6):9947-9960. PubMed ID: 28039480
[TBL] [Abstract][Full Text] [Related]
31. Birt-Hogg-Dube syndrome: clinicopathological features of the lung.
Furuya M; Nakatani Y
J Clin Pathol; 2013 Mar; 66(3):178-86. PubMed ID: 23223565
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. 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]
34. 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]
35. Genetic screening of the FLCN gene identify six novel variants and a Danish founder mutation.
Rossing M; Albrechtsen A; Skytte AB; Jensen UB; Ousager LB; Gerdes AM; Nielsen FC; Hansen TV
J Hum Genet; 2017 Feb; 62(2):151-157. PubMed ID: 27734835
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. 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]
38. 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]
39. A case of Birt-Hogg-Dubé syndrome presenting with a single pedunculated fibrofolliculoma and a novel FLCN gene mutation.
César A; Baudrier T; Mota A; Azevedo F
Actas Dermosifiliogr; 2016; 107(6):541-3. PubMed ID: 27083392
[No Abstract] [Full Text] [Related]
40. A retrospective two centre study of Birt-Hogg-Dubé syndrome reveals a pathogenic founder mutation in FLCN in the Swedish population.
Lagerstedt-Robinson K; Baranowska Körberg I; Tsiaprazis S; Björck E; Tham E; Poluha A; Hellström Pigg M; Paulsson-Karlsson Y; Nordenskjöld M; Johansson-Soller M; Aravidis C
PLoS One; 2022; 17(2):e0264056. PubMed ID: 35176117
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
