530 related articles for article (PubMed ID: 16767671)
1. [A research on TGFBI gene mutations in Chinese families with corneal dystrophies].
Qi YH; He HD; Li Y; Lin H; Gu JZ; Su H; Huang SZ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Jun; 23(3):310-2. PubMed ID: 16767671
[TBL] [Abstract][Full Text] [Related]
2. TGFBI (BIGH3) gene mutations in Hungary--report of the novel F547S mutation associated with polymorphic corneal amyloidosis.
Takács L; Losonczy G; Matesz K; Balogh I; Sohajda Z; Tóth K; Fazakas F; Vereb G; Berta A
Mol Vis; 2007 Oct; 13():1976-83. PubMed ID: 17982422
[TBL] [Abstract][Full Text] [Related]
3. TGFBI gene mutations in Brazilian patients with corneal dystrophy.
Solari HP; Ventura MP; Perez AB; Sallum JM; Burnier MN; Belfort R
Eye (Lond); 2007 May; 21(5):587-90. PubMed ID: 16440005
[TBL] [Abstract][Full Text] [Related]
4. Spontaneous and inheritable R555Q mutation in the TGFBI/BIGH3 gene in two unrelated families exhibiting Bowman's layer corneal dystrophy.
Zhao XC; Nakamura H; Subramanyam S; Stock LE; Gillette TE; Yoshikawa S; Ma X; Yee RW
Ophthalmology; 2007 Nov; 114(11):e39-46. PubMed ID: 17980739
[TBL] [Abstract][Full Text] [Related]
5. A mutation within exon 14 of the TGFBI (BIGH3) gene on chromosome 5q31 causes an asymmetric, late-onset form of lattice corneal dystrophy.
Stewart H; Black GC; Donnai D; Bonshek RE; McCarthy J; Morgan S; Dixon MJ; Ridgway AA
Ophthalmology; 1999 May; 106(5):964-70. PubMed ID: 10328397
[TBL] [Abstract][Full Text] [Related]
6. [Identification of BIGH3 gene mutations in the patients with two types of corneal dystrophies].
Jin T; Zou LH; Yang L; Dong WL; Yu J; Lu L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Feb; 21(1):32-4. PubMed ID: 14767905
[TBL] [Abstract][Full Text] [Related]
7. In vivo laser confocal microscopy findings for Bowman's layer dystrophies (Thiel-Behnke and Reis-Bücklers corneal dystrophies).
Kobayashi A; Sugiyama K
Ophthalmology; 2007 Jan; 114(1):69-75. PubMed ID: 17198850
[TBL] [Abstract][Full Text] [Related]
8. Mutation analysis of the TGFBI gene in Vietnamese with granular and Avellino corneal dystrophy.
Cung le X; Ha NT; Chau HM; Thanh TK; Fujiki K; Murakami A; Hiratsuka Y; Kanai A
Jpn J Ophthalmol; 2004; 48(1):12-6. PubMed ID: 14767644
[TBL] [Abstract][Full Text] [Related]
9. A unique corneal dystrophy of Bowman's layer and stroma associated with the Gly623Asp mutation in the transforming growth factor beta-induced (TGFBI) gene.
Aldave AJ; Rayner SA; King JA; Affeldt JA; Yellore VS
Ophthalmology; 2005 Jun; 112(6):1017-22. PubMed ID: 15885785
[TBL] [Abstract][Full Text] [Related]
10. [Analysis of mutation of BIGH3 gene in Chinese patients with corneal dystrophies].
Yu J; Zou LH; He JC; Liu NP; Zhang W; Lu L; Sun XG; Dong DS; Wu YY; Yin XT
Zhonghua Yan Ke Za Zhi; 2003 Oct; 39(10):582-6. PubMed ID: 14766070
[TBL] [Abstract][Full Text] [Related]
11. Phenotype associated with the H626P mutation and other changes in the TGFBI gene in Czech families.
Liskova P; Klintworth GK; Bowling BL; Filipec M; Jirsova K; Tuft SJ; Bhattacharya SS; Hardcastle AJ; Ebenezer ND
Ophthalmic Res; 2008; 40(2):105-8. PubMed ID: 18259096
[TBL] [Abstract][Full Text] [Related]
12. TGFBI gene mutation analysis in families with hereditary corneal dystrophies from Ukraine.
Pampukha VM; Drozhyna GI; Livshits LA
Ophthalmologica; 2004; 218(6):411-4. PubMed ID: 15564760
[TBL] [Abstract][Full Text] [Related]
13. TGFBI mutational analysis in a New Zealand population of inherited corneal dystrophy patients.
Vincent AL; de Karolyi B; Patel DV; Wheeldon CE; McGhee CN
Br J Ophthalmol; 2010 Jul; 94(7):836-42. PubMed ID: 19948560
[TBL] [Abstract][Full Text] [Related]
14. TGFBI (BIGH3) gene mutations in German families: two novel mutations associated with unique clinical and histopathological findings.
Gruenauer-Kloevekorn C; Clausen I; Weidle E; Wolter-Roessler M; Tost F; Völcker HE; Schulze DP; Heinritz W; Reinhard T; Froster U; Duncker G; Schorderet D; Auw-Haedrich C
Br J Ophthalmol; 2009 Jul; 93(7):932-7. PubMed ID: 19001012
[TBL] [Abstract][Full Text] [Related]
15. Corneal dystrophies in Japan.
Fujiki K; Nakayasu K; Kanai A
J Hum Genet; 2001; 46(8):431-5. PubMed ID: 11501939
[TBL] [Abstract][Full Text] [Related]
16. A novel variant lattice corneal dystrophy caused by association of mutation (V625D) in TGFBI gene.
Tian X; Fujiki K; Zhang Y; Murakami A; Li Q; Kanai A; Wang W; Hao Y; Ma Z
Am J Ophthalmol; 2007 Sep; 144(3):473-5. PubMed ID: 17765440
[TBL] [Abstract][Full Text] [Related]
17. [Molecular genetic analysis of the BIGH3 gene in lattice type I (Biber-Haab-Dimmer) and granular type II (Avellino) corneal dystrophy: is indirect mutation analysis for hot spots recommended?].
Grünauer-Kloevekorn C; Bräutigam S; Wolter-Roessler M; Tost F; Weidle E; Froster U; Duncker GI
Klin Monbl Augenheilkd; 2005 Dec; 222(12):1017-23. PubMed ID: 16380889
[TBL] [Abstract][Full Text] [Related]
18. Expanding the mutational spectrum in TGFBI-linked corneal dystrophies: Identification of a novel and unusual mutation (Val113Ile) in a family with granular dystrophy.
Zenteno JC; Ramirez-Miranda A; Santacruz-Valdes C; Suarez-Sanchez R
Mol Vis; 2006 Apr; 12():331-5. PubMed ID: 16636649
[TBL] [Abstract][Full Text] [Related]
19. Severe corneal dystrophy phenotype caused by homozygous R124H keratoepithelin mutations.
Okada M; Yamamoto S; Inoue Y; Watanabe H; Maeda N; Shimomura Y; Ishii Y; Tano Y
Invest Ophthalmol Vis Sci; 1998 Sep; 39(10):1947-53. PubMed ID: 9727418
[TBL] [Abstract][Full Text] [Related]
20. The TGFBI A546D mutation causes an atypical type of lattice corneal dystrophy.
Correa-Gomez V; Villalvazo-Cordero L; Zenteno JC
Mol Vis; 2007 Sep; 13():1695-700. PubMed ID: 17893671
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]