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173 related items for PubMed ID: 22211584
1. FLCN gene-mutated renal cell neoplasms: mother and daughter cases with a novel germline mutation. Nagashima Y, Furuya M, Gotohda H, Takagi S, Hes O, Michal M, Grossmann P, Tanaka R, Nakatani Y, Kuroda N. Int J Urol; 2012 May; 19(5):468-70. PubMed ID: 22211584 [Abstract] [Full Text] [Related]
2. 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]
3. 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 [Abstract] [Full Text] [Related]
4. Heterozygous germline FLCN mutation in Birt-Hogg-Dubé syndrome with bilateral renal hybrid oncocytic/chromophobe tumor and unilateral renal chromophobe cell carcinoma: a case report. Li J, Liu F, Liu X, Hu Y, Liu Z, Shen Y, Wan J. J Cancer Res Clin Oncol; 2023 Jun; 149(6):2319-2325. PubMed ID: 36258004 [Abstract] [Full Text] [Related]
5. 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]
6. Intratumoral peripheral small papillary tufts: a diagnostic clue of renal tumors associated with Birt-Hogg-Dubé syndrome. Kuroda N, Furuya M, Nagashima Y, Gotohda H, Moritani S, Kawakami F, Imamura Y, Bando Y, Takahashi M, Kanayama HO, Ota S, Michal M, Hes O, Nakatani Y. Ann Diagn Pathol; 2014 Jun; 18(3):171-6. PubMed ID: 24767893 [Abstract] [Full Text] [Related]
7. 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 [Abstract] [Full Text] [Related]
8. A case of Birt-Hogg-Dubé syndrome implying reduced or no wild-type folliculin without mutated protein is pathogenic. Enomoto Y, Namba Y, Hoshika Y, Komemushi Y, Mitani K, Kume H, Kobayashi E, Miyama Y, Homma Y, Ushiku T, Seyama K. Eur J Med Genet; 2020 Apr; 63(4):103820. PubMed ID: 31778855 [Abstract] [Full Text] [Related]
9. Immunohistochemical characterization of renal tumors in patients with Birt-Hogg-Dubé syndrome. Iribe Y, Kuroda N, Nagashima Y, Yao M, Tanaka R, Gotoda H, Kawakami F, Imamura Y, Nakamura Y, Ando M, Araki A, Matsushima J, Nakatani Y, Furuya M. Pathol Int; 2015 Mar; 65(3):126-32. PubMed ID: 25597876 [Abstract] [Full Text] [Related]
10. 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 [Abstract] [Full Text] [Related]
11. Fluorescent and chromogenic in situ hybridization of CEN17q as a potent useful diagnostic marker for Birt-Hogg-Dubé syndrome-associated chromophobe renal cell carcinomas. Kato I, Iribe Y, Nagashima Y, Kuroda N, Tanaka R, Nakatani Y, Hasumi H, Yao M, Furuya M. Hum Pathol; 2016 Jun; 52():74-82. PubMed ID: 26980015 [Abstract] [Full Text] [Related]
12. 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]
13. Early onset renal cell carcinoma in an adolescent girl with germline FLCN exon 5 deletion. Schneider M, Dinkelborg K, Xiao X, Chan-Smutko G, Hruska K, Huang D, Sagar P, Harisinghani M, Iliopoulos O. Fam Cancer; 2018 Jan; 17(1):135-139. PubMed ID: 28623476 [Abstract] [Full Text] [Related]
14. Investigation of the Birt-Hogg-Dube tumour suppressor gene (FLCN) in familial and sporadic colorectal cancer. Nahorski MS, Lim DH, Martin L, Gille JJ, McKay K, Rehal PK, Ploeger HM, van Steensel M, Tomlinson IP, Latif F, Menko FH, Maher ER. J Med Genet; 2010 Jun; 47(6):385-90. PubMed ID: 20522427 [Abstract] [Full Text] [Related]
15. 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; 52(3):323-6. PubMed ID: 23414156 [Abstract] [Full Text] [Related]
16. Establishment and characterization of BHD-F59RSVT, an immortalized cell line derived from a renal cell carcinoma in a patient with Birt-Hogg-Dubé syndrome. Furuya M, Hasumi H, Baba M, Tanaka R, Iribe Y, Onishi T, Nagashima Y, Nakatani Y, Isono Y, Yao M. Lab Invest; 2017 Mar; 97(3):343-351. PubMed ID: 27991910 [Abstract] [Full Text] [Related]
17. Genome-Wide Uniparental Disomy and Copy Number Variations in Renal Cell Carcinomas Associated with Birt-Hogg-Dubé Syndrome. Iribe Y, Yao M, Tanaka R, Kuroda N, Nagashima Y, Nakatani Y, Furuya M. Am J Pathol; 2016 Feb; 186(2):337-46. PubMed ID: 26776076 [Abstract] [Full Text] [Related]
18. Birt-Hogg-Dubé syndrome with clear-cell and oncocytic renal tumour and trichoblastoma associated with a novel FLCN mutation. Imada K, Dainichi T, Yokomizo A, Tsunoda T, Song YH, Nagasaki A, Sawamura D, Nishie W, Shimizu H, Fukagawa S, Urabe K, Furue M, Hashimoto T, Naito S. Br J Dermatol; 2009 Jun; 160(6):1350-3. PubMed ID: 19416240 [No Abstract] [Full Text] [Related]
19. [DIAGNOSIS OF GENETIC VARIANT CARRIERS IN A PATIENT WITH ASYMPTOMATIC BIRT-HOGG-DUBÉ SYNDROME: A CASE REPORT]. Watari S, Ichikawa T, Hirasawa A, Shiraishi H, Tokunaga M, Kubota R, Kusumi N, Tsushima T, Shinno Y, Furuya M. Nihon Hinyokika Gakkai Zasshi; 2023 Jun; 114(2):61-65. PubMed ID: 38644188 [Abstract] [Full Text] [Related]
20. Renal tumour suppressor function of the Birt-Hogg-Dubé syndrome gene product folliculin. Hudon V, Sabourin S, Dydensborg AB, Kottis V, Ghazi A, Paquet M, Crosby K, Pomerleau V, Uetani N, Pause A. J Med Genet; 2010 Mar; 47(3):182-9. PubMed ID: 19843504 [Abstract] [Full Text] [Related] Page: [Next] [New Search]