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346 related items for PubMed ID: 19416240
1. 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]
2. Birt-Hogg-Dubé (BHD) syndrome: report of two novel germline mutations in the folliculin (FLCN) gene. Palmirotta R, Donati P, Savonarola A, Cota C, Ferroni P, Guadagni F. Eur J Dermatol; 2008 Jun; 18(4):382-6. PubMed ID: 18573707 [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. [Birt-Hogg-Dubé syndrome]. Rehfeld A, van Steensel MA, Friis-Hansen L. Ugeskr Laeger; 2010 Jul 19; 172(29):2085-90. PubMed ID: 20633341 [Abstract] [Full Text] [Related]
5. Novel mutations in the BHD gene and absence of loss of heterozygosity in fibrofolliculomas of Birt-Hogg-Dubé patients. van Steensel MA, Verstraeten VL, Frank J, Kelleners-Smeets NW, Poblete-Gutiérrez P, Marcus-Soekarman D, Bladergroen RS, Steijlen PM, van Geel M. J Invest Dermatol; 2007 Mar 19; 127(3):588-93. PubMed ID: 17124507 [Abstract] [Full Text] [Related]
6. A novel familial germline mutation in the initiator codon of the BHD gene in a patient with Birt-Hogg-Dubé syndrome. Bessis D, Giraud S, Richard S. Br J Dermatol; 2006 Nov 19; 155(5):1067-9. PubMed ID: 17034545 [No Abstract] [Full Text] [Related]
7. [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 Nov 19; 153():A581. PubMed ID: 19857281 [Abstract] [Full Text] [Related]
8. 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 19; 23(3):204-10. PubMed ID: 26608100 [Abstract] [Full Text] [Related]
9. Interaction of folliculin (Birt-Hogg-Dubé gene product) with a novel Fnip1-like (FnipL/Fnip2) protein. Takagi Y, Kobayashi T, Shiono M, Wang L, Piao X, Sun G, Zhang D, Abe M, Hagiwara Y, Takahashi K, Hino O. Oncogene; 2008 Sep 11; 27(40):5339-47. PubMed ID: 18663353 [Abstract] [Full Text] [Related]
10. Detection of 1733insC mutations in an Asian family with Birt-Hogg-Dubé syndrome. Kawasaki H, Sawamura D, Nakazawa H, Hattori N, Goto M, Sato-Matsumura KC, Akiyama M, Shimizu H. Br J Dermatol; 2005 Jan 11; 152(1):142-5. PubMed ID: 15656814 [Abstract] [Full Text] [Related]
11. Re: Chromophobe renal cell carcinoma in a patient with the Birt-Hogg-Dube syndrome. Walther MM, Grubb RL. J Urol; 2003 Jun 11; 169(6):2303-4. PubMed ID: 12771781 [No Abstract] [Full Text] [Related]
12. 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 11; 47(6):385-90. PubMed ID: 20522427 [Abstract] [Full Text] [Related]
13. Early onset of renal cancer in a family with Birt-Hogg-Dubé syndrome. Kluijt I, de Jong D, Teertstra HJ, Axwijk PH, Gille JJ, Bell K, van Rens A, van der Velden AW, Middelton L, Horenblas S. Clin Genet; 2009 Jun 11; 75(6):537-43. PubMed ID: 19320655 [Abstract] [Full Text] [Related]
14. 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 11; 47(3):182-9. PubMed ID: 19843504 [Abstract] [Full Text] [Related]
15. 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 11; 106(3):315-23. PubMed ID: 25594584 [Abstract] [Full Text] [Related]
16. Deficiency of FLCN in mouse kidney led to development of polycystic kidneys and renal neoplasia. Chen J, Futami K, Petillo D, Peng J, Wang P, Knol J, Li Y, Khoo SK, Huang D, Qian CN, Zhao P, Dykema K, Zhang R, Cao B, Yang XJ, Furge K, Williams BO, Teh BT. PLoS One; 2008 Mar 11; 3(10):e3581. PubMed ID: 18974783 [Abstract] [Full Text] [Related]
17. [Intra- and interfamilial phenotype variation in Birt-Hogg-Dubé syndrome: Consequences for therapy]. Steff M, Bourillon A, Frebourg T, Balderi X, Descamps V, Joly P, Piette F, Crestani B, Grandchamp B, Soufir N. Ann Dermatol Venereol; 2010 Mar 11; 137(3):203-7. PubMed ID: 20227563 [Abstract] [Full Text] [Related]
18. 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 11; 19(5):468-70. PubMed ID: 22211584 [Abstract] [Full Text] [Related]
19. A new locus-specific database (LSDB) for mutations in the folliculin (FLCN) gene. Lim DH, Rehal PK, Nahorski MS, Macdonald F, Claessens T, Van Geel M, Gijezen L, Gille JJ, Giraud S, Richard S, van Steensel M, Menko FH, Maher ER. Hum Mutat; 2010 Jan 11; 31(1):E1043-51. PubMed ID: 19802896 [Abstract] [Full Text] [Related]
20. 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 11; 50(8):968-71. PubMed ID: 21781069 [Abstract] [Full Text] [Related] Page: [Next] [New Search]