173 related articles for article (PubMed ID: 11927442)
1. Clinical outcome of eight BIGH3-linked corneal dystrophies.
Ellies P; Renard G; Valleix S; Boelle PY; Dighiero P
Ophthalmology; 2002 Apr; 109(4):793-7. PubMed ID: 11927442
[TBL] [Abstract][Full Text] [Related]
2. Phototherapeutic keratectomy for BIGH3-linked corneal dystrophy recurring after penetrating keratoplasty.
Ellies P; Bejjani RA; Bourges JL; Boelle PY; Renard G; Dighiero P
Ophthalmology; 2003 Jun; 110(6):1119-25. PubMed ID: 12799235
[TBL] [Abstract][Full Text] [Related]
3. BIGH3 mutation spectrum in corneal dystrophies.
Munier FL; Frueh BE; Othenin-Girard P; Uffer S; Cousin P; Wang MX; Héon E; Black GC; Blasi MA; Balestrazzi E; Lorenz B; Escoto R; Barraquer R; Hoeltzenbein M; Gloor B; Fossarello M; Singh AD; Arsenijevic Y; Zografos L; Schorderet DF
Invest Ophthalmol Vis Sci; 2002 Apr; 43(4):949-54. PubMed ID: 11923233
[TBL] [Abstract][Full Text] [Related]
4. Clinical, histologic, and ultrastructural features of the corneal dystrophy caused by the R124L mutation of the BIGH3 gene.
Dighiero P; Valleix S; D'Hermies F; Drunat S; Ellies P; Savoldelli M; Pouliquen Y; Delpech M; Legeais JM; Renard G
Ophthalmology; 2000 Jul; 107(7):1353-7. PubMed ID: 10889112
[TBL] [Abstract][Full Text] [Related]
5. An analysis of BIGH3 mutations in patients with corneal dystrophies in the Kyushu district of Japan.
Yoshida S; Kumano Y; Yoshida A; Hisatomi T; Matsui H; Nishida T; Ishibashi T; Matsui T
Jpn J Ophthalmol; 2002; 46(4):469-71. PubMed ID: 12225829
[TBL] [Abstract][Full Text] [Related]
6. Survey of patients with granular, lattice, avellino, and Reis-Bücklers corneal dystrophies for mutations in the BIGH3 and gelsolin genes.
Afshari NA; Mullally JE; Afshari MA; Steinert RF; Adamis AP; Azar DT; Talamo JH; Dohlman CH; Dryja TP
Arch Ophthalmol; 2001 Jan; 119(1):16-22. PubMed ID: 11146721
[TBL] [Abstract][Full Text] [Related]
7. Histologic phenotype-genotype correlation of corneal dystrophies associated with eight distinct mutations in the TGFBI gene.
Dighiero P; Niel F; Ellies P; D'Hermies F; Savoldelli M; Renard G; Delpech M; Valleix S
Ophthalmology; 2001 Apr; 108(4):818-23. PubMed ID: 11297504
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. [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]
10. The classic form of granular corneal dystrophy associated with R555W mutation in the BIGH3 gene is rare in Japanese patients.
Konishi M; Mashima Y; Yamada M; Kudoh J; Shimizu N
Am J Ophthalmol; 1998 Sep; 126(3):450-2. PubMed ID: 9744382
[TBL] [Abstract][Full Text] [Related]
11. BIGH3 gene mutations and rapid detection in Korean patients with corneal dystrophy.
Kim HS; Yoon SK; Cho BJ; Kim EK; Joo CK
Cornea; 2001 Nov; 20(8):844-9. PubMed ID: 11685063
[TBL] [Abstract][Full Text] [Related]
12. H626R and R124C mutations of the TGFBI (BIGH3) gene caused lattice corneal dystrophy in Vietnamese people.
Chau HM; Ha NT; Cung LX; Thanh TK; Fujiki K; Murakami A; Kanai A
Br J Ophthalmol; 2003 Jun; 87(6):686-9. PubMed ID: 12770961
[TBL] [Abstract][Full Text] [Related]
13. Six different mutations of TGFBI (betaig-h3, keratoepithelin) gene found in Japanese corneal dystrophies.
Fujiki K; Hotta Y; Nakayasu K; Yamaguchi T; Kato T; Uesugi Y; Ha NT; Endo S; Ishida N; Lu WN; Kanai A
Cornea; 2000 Nov; 19(6):842-5. PubMed ID: 11095060
[TBL] [Abstract][Full Text] [Related]
14. The spectrum of beta ig-h3 gene mutations in Japanese patients with corneal dystrophy.
Yamamoto S; Okada M; Tsujikawa M; Morimura H; Maeda N; Watanabe H; Inoue Y; Shimomura Y; Kinoshita S; Tano Y
Cornea; 2000 May; 19(3 Suppl):S21-3. PubMed ID: 10832717
[TBL] [Abstract][Full Text] [Related]
15. A clinical and molecular genetic study of autosomal-dominant stromal corneal dystrophy in British population.
El-Ashry MF; Abd El-Aziz MM; Hardcastle AJ; Bhattacharya SS; Ebenezer ND
Ophthalmic Res; 2005; 37(6):310-7. PubMed ID: 16118514
[TBL] [Abstract][Full Text] [Related]
16. Immunohistology of kerato-epithelin in corneal stromal dystrophies associated with R124 mutations of the BIGH3 gene.
Konishi M; Yamada M; Nakamura Y; Mashima Y
Curr Eye Res; 2000 Nov; 21(5):891-6. PubMed ID: 11262611
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. BIGH3 exon 14 mutations lead to intermediate type I/IIIA of lattice corneal dystrophies.
Schmitt-Bernard CF; Guittard C; Arnaud B; Demaille J; Argiles A; Claustres M; Tuffery-Giraud S
Invest Ophthalmol Vis Sci; 2000 May; 41(6):1302-8. PubMed ID: 10798644
[TBL] [Abstract][Full Text] [Related]
19. An autosomal dominant granular corneal dystrophy family associated with R555W mutation in the BIGH3 gene.
Hou YC; Hu FR; Chen MS
J Formos Med Assoc; 2003 Feb; 102(2):117-20. PubMed ID: 12709742
[TBL] [Abstract][Full Text] [Related]
20. [Molecular genetic study on patients with lattice corneal dystrophy in China].
Dong WL; Zou LH; Pan ZQ; Jin T; Yu J
Zhonghua Yan Ke Za Zhi; 2005 Jun; 41(6):523-6. PubMed ID: 16008913
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
