396 related articles for article (PubMed ID: 15177960)
1. Polymorphic corneal amyloidosis: a disorder due to a novel mutation in the transforming growth factor beta-induced (BIGH3) gene.
Eifrig DE; Afshari NA; Buchanan HW; Bowling BL; Klintworth GK
Ophthalmology; 2004 Jun; 111(6):1108-14. PubMed ID: 15177960
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. No pathogenic mutations identified in the TGFBI gene in polymorphic corneal amyloid deposition.
Aldave AJ; Rayner SA; King JA; Salem AK; Prechanond A; Hashida S; Affeldt JC; Meallet MA; Glasgow BJ; Small KW; Yellore VS
Cornea; 2006 May; 25(4):413-5. PubMed ID: 16670477
[TBL] [Abstract][Full Text] [Related]
5. A corneal dystrophy associated with transforming growth factor beta-induced Gly623Asp mutation an amyloidogenic phenotype.
Auw-Haedrich C; Agostini H; Clausen I; Reinhard T; Eberwein P; Schorderet DF; Gruenauer-Kloevekorn C
Ophthalmology; 2009 Jan; 116(1):46-51. PubMed ID: 19019446
[TBL] [Abstract][Full Text] [Related]
6. Lattice corneal dystrophy associated with the Ala546Asp and Pro551Gln missense changes in the TGFBI gene.
Aldave AJ; Gutmark JG; Yellore VS; Affeldt JA; Meallet MA; Udar N; Rao NA; Small KW; Klintworth GK
Am J Ophthalmol; 2004 Nov; 138(5):772-81. PubMed ID: 15531312
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Hereditary lattice corneal dystrophy is associated with corneal amyloid deposits enclosing C-terminal fragments of keratoepithelin.
Stix B; Leber M; Bingemer P; Gross C; Rüschoff J; Fändrich M; Schorderet DF; Vorwerk CK; Zacharias M; Roessner A; Röcken C
Invest Ophthalmol Vis Sci; 2005 Apr; 46(4):1133-9. PubMed ID: 15790870
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Two mutations in the TGFBI (BIGH3) gene associated with lattice corneal dystrophy in an extensively studied family.
Klintworth GK; Bao W; Afshari NA
Invest Ophthalmol Vis Sci; 2004 May; 45(5):1382-8. PubMed ID: 15111592
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. [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]
15. Clinical and genetic features of TGFBI-linked corneal dystrophies in Mexican population: description of novel mutations and novel genotype-phenotype correlations.
Zenteno JC; Correa-Gomez V; Santacruz-Valdez C; Suarez-Sanchez R; Villanueva-Mendoza C
Exp Eye Res; 2009 Aug; 89(2):172-7. PubMed ID: 19303004
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Novel L558P mutation of the TGFBI gene found in Ukrainian families with atypical corneal dystrophy.
Pampukha VM; Kravchenko SA; Tereshchenko FA; Livshits LA; Drozhyna GI
Ophthalmologica; 2009; 223(3):207-14. PubMed ID: 19221447
[TBL] [Abstract][Full Text] [Related]
18. [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]
19. Late-onset lattice corneal dystrophy without typical lattice lines caused by a novel mutation in the TGFBI gene.
Ołdak M; Szaflik JP; Ścieżyńska A; Udziela M; Maksym RB; Rymgayłło-Jankowska B; Hofmann-Rummelt C; Menzel-Severing J; Płoski R; Żarnowski T; Kruse FE; Szaflik J
Cornea; 2014 Mar; 33(3):294-9. PubMed ID: 24473223
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]