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Journal Abstract Search
172 related items for PubMed ID: 25408992
1. Birt-Hogg-Dubé syndrome in an African patient and a novel mutation in the FLCN gene. Pritchett EN, Kim J, Patel K, Patel T, Cusack CA. JAMA Dermatol; 2015 Mar; 151(3):348-9. PubMed ID: 25408992 [No Abstract] [Full Text] [Related]
2. 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 Mar; 107(6):541-3. PubMed ID: 27083392 [No Abstract] [Full Text] [Related]
3. Birt-Hogg-Dubé syndrome: Clinical and molecular aspects of recently identified kidney cancer syndrome. Hasumi H, Baba M, Hasumi Y, Furuya M, Yao M. Int J Urol; 2016 Mar; 23(3):204-10. PubMed ID: 26608100 [Abstract] [Full Text] [Related]
4. Birt-Hogg-Dubé syndrome with novel FLCN gene mutations and different clinical presentations: Case series. Erinç A, Azakli D, Kirhan G, Satici C. Tuberk Toraks; 2024 Mar; 72(1):91-94. PubMed ID: 38676598 [No Abstract] [Full Text] [Related]
5. Distinctive expression patterns of glycoprotein non-metastatic B and folliculin in renal tumors in patients with Birt-Hogg-Dubé syndrome. Furuya M, Hong SB, Tanaka R, Kuroda N, Nagashima Y, Nagahama K, Suyama T, Yao M, Nakatani Y. Cancer Sci; 2015 Mar; 106(3):315-23. PubMed ID: 25594584 [Abstract] [Full Text] [Related]
6. 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 [Abstract] [Full Text] [Related]
7. Late onset of skin manifestations in Birt-Hogg-Dubé syndrome with FLCN mutation p.W260X. Sattler EC, Lang MU, van Steensel MA, van Geel M, Schneider JJ, Flaig MJ, Ruzicka T, Burgdorf W, Steinlein OK. Acta Derm Venereol; 2012 Mar; 92(2):187-8. PubMed ID: 22068306 [No Abstract] [Full Text] [Related]
8. An inherited cause of pneumothorax--the Birt-Hogg-Dubé syndrome. Zenone T. QJM; 2014 May; 107(5):393-4. PubMed ID: 23904515 [No Abstract] [Full Text] [Related]
9. 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 22; 19(1):14. PubMed ID: 29357828 [Abstract] [Full Text] [Related]
10. 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 16; 19(1):45. PubMed ID: 29548312 [Abstract] [Full Text] [Related]
11. [Birt-Hogg-Dubé syndrome]. Křepelová A, Puchmajerová A, Vasovčák P, Chocholatý M. Klin Onkol; 2012 Mar 16; 25 Suppl():S18-20. PubMed ID: 22920201 [Abstract] [Full Text] [Related]
12. 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 16; 21(10):632-634. PubMed ID: 28805452 [Abstract] [Full Text] [Related]
14. Birt-Hogg-Dubé syndrome in a patient with melanoma and a novel mutation in the FCLN gene. Mota-Burgos A, Acosta EH, Márquez FV, Mendiola M, Herrera-Ceballos E. Int J Dermatol; 2013 Mar 12; 52(3):323-6. PubMed ID: 23414156 [Abstract] [Full Text] [Related]
16. 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 12; 35(2):241-5. PubMed ID: 23542717 [Abstract] [Full Text] [Related]
17. 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]
18. Birt-Hogg-Dubé syndrome: a rare cause of familial spontaneous pneumothorax. Luk HM, Tong TM, Lo IF. Hong Kong Med J; 2017 Aug 26; 23(4):416.e4-5. PubMed ID: 28775225 [No Abstract] [Full Text] [Related]
19. 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 02; 11(1):42. PubMed ID: 29720200 [Abstract] [Full Text] [Related]
20. 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] Page: [Next] [New Search]