These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

193 related articles for article (PubMed ID: 34000505)

  • 1. Colorectal cancer risk in families with Birt-Hogg-Dubé syndrome increased.
    Sattler EC; Syunyaeva Z; Reithmair M; Dempke W; Steinlein OK
    Eur J Cancer; 2021 Jul; 151():168-174. PubMed ID: 34000505
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 98(2):125-132. PubMed ID: 31266032
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Birt-Hogg-Dube Syndrome with a Novel Mutation in the FLCN Gene.
    Kayhan G; Yılmaz Demirci N; Turktas H; Ergun MA
    Genet Test Mol Biomarkers; 2017 Oct; 21(10):632-634. PubMed ID: 28805452
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. Birt-Hogg-Dubé syndrome. State-of-the-art review with emphasis on pulmonary involvement.
    Dal Sasso AA; Belém LC; Zanetti G; Souza CA; Escuissato DL; Irion KL; Guimarães MD; Marchiori E
    Respir Med; 2015 Mar; 109(3):289-96. PubMed ID: 25519092
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Birt-Hogg-Dubé syndrome].
    Křepelová A; Puchmajerová A; Vasovčák P; Chocholatý M
    Klin Onkol; 2012; 25 Suppl():S18-20. PubMed ID: 22920201
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Haploinsufficiency of the folliculin gene leads to impaired functions of lung fibroblasts in patients with Birt-Hogg-Dubé syndrome.
    Hoshika Y; Takahashi F; Togo S; Hashimoto M; Nara T; Kobayashi T; Nurwidya F; Kataoka H; Kurihara M; Kobayashi E; Ebana H; Kikkawa M; Ando K; Nishino K; Hino O; Takahashi K; Seyama K
    Physiol Rep; 2016 Nov; 4(21):. PubMed ID: 27905298
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Pneumothorax developing for the first time in a 73-year-old woman diagnosed with Birt-Hogg-Dubé syndrome.
    Kunogi Okura M; Yae T; Nagashima O; Hirai S; Kumasaka T; Iwase A
    Intern Med; 2013; 52(21):2453-5. PubMed ID: 24190151
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Kidney cancer characteristics and genotype-phenotype-correlations in Birt-Hogg-Dubé syndrome.
    Sattler EC; Reithmair M; Steinlein OK
    PLoS One; 2018; 13(12):e0209504. PubMed ID: 30586397
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Birt-Hogg-Dubé syndrome encountered at rare lung disease clinic in Anhui province, China.
    Zhang G; Liu J; Wang Y; Wang Y; Jiang X; Peng Y; Xiao J; Wei W; Shen B; Yi L; Ryu JH; Hu X
    Orphanet J Rare Dis; 2022 May; 17(1):203. PubMed ID: 35578266
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Birt-Hogg-Dubé syndrome and familial adenomatous polyposis: an association or a coincidence?
    Kashiwada T; Shimizu H; Tamura K; Seyama K; Horie Y; Mizoo A
    Intern Med; 2012; 51(13):1789-92. PubMed ID: 22790147
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. BHD mutations, clinical and molecular genetic investigations of Birt-Hogg-Dubé syndrome: a new series of 50 families and a review of published reports.
    Toro JR; Wei MH; Glenn GM; Weinreich M; Toure O; Vocke C; Turner M; Choyke P; Merino MJ; Pinto PA; Steinberg SM; Schmidt LS; Linehan WM
    J Med Genet; 2008 Jun; 45(6):321-31. PubMed ID: 18234728
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.