391 related articles for article (PubMed ID: 14767905)
21. BIGH3 mutation in a Bangladeshi family with a variable phenotype of LCDI.
El-Ashry MF; Abd El-Aziz MM; Ficker LA; Hardcastle AJ; Bhattacharya SS; Ebenezer ND
Eye (Lond); 2004 Jul; 18(7):723-8. PubMed ID: 15017378
[TBL] [Abstract][Full Text] [Related]
22. Detection of the most common corneal dystrophies caused by BIGH3 gene point mutations using a multispot gold-capped nanoparticle array chip.
Yoo SY; Kim DK; Park TJ; Kim EK; Tamiya E; Lee SY
Anal Chem; 2010 Feb; 82(4):1349-57. PubMed ID: 20092310
[TBL] [Abstract][Full Text] [Related]
23. TGFBI gene mutations causing lattice and granular corneal dystrophies in Indian patients.
Chakravarthi SV; Kannabiran C; Sridhar MS; Vemuganti GK
Invest Ophthalmol Vis Sci; 2005 Jan; 46(1):121-5. PubMed ID: 15623763
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. 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]
26. 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]
27. 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]
28. Homozygotic patient with betaig-h3 gene mutation in granular dystrophy.
Fujiki K; Hotta Y; Nakayasu K; Kanai A
Cornea; 1998 May; 17(3):288-92. PubMed ID: 9603385
[TBL] [Abstract][Full Text] [Related]
29. Exacerbation of Avellino corneal dystrophy after LASIK in North America.
Banning CS; Kim WC; Randleman JB; Kim EK; Stulting RD
Cornea; 2006 May; 25(4):482-4. PubMed ID: 16670492
[TBL] [Abstract][Full Text] [Related]
30. De novo mutation in the BIGH3/TGFB1 gene causing granular corneal dystrophy.
Hilton EN; Black GC; Manson FD; Schorderet DF; Munier FL
Br J Ophthalmol; 2007 Aug; 91(8):1083-4. PubMed ID: 17638818
[No Abstract] [Full Text] [Related]
31. Development of a DNA chip for the diagnosis of the most common corneal dystrophies caused by mutations in the betaigh3 gene.
Yoo SY; Kim TI; Lee SY; Kim EK; Keum KC; Yoo NC; Yoo WM
Br J Ophthalmol; 2007 Jun; 91(6):722-7. PubMed ID: 17215264
[TBL] [Abstract][Full Text] [Related]
32. Ultrastructural and molecular analysis of Bowman's layer corneal dystrophies: an epithelial origin?
Ridgway AE; Akhtar S; Munier FL; Schorderet DF; Stewart H; Perveen R; Bonshek RE; Odenthal MT; Dixon M; Barraquer R; Escoto R; Black GC
Invest Ophthalmol Vis Sci; 2000 Oct; 41(11):3286-92. PubMed ID: 11006215
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. 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]
35. 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]
36. 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]
37. 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]
38. 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]
39. 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]
40. R555W mutation of TGFbetaI related to granular corneal dystrophy in Chinese patients.
Hu L; Xu F; Ma WJ; Zhang H; Sui RF
Chin Med J (Engl); 2009 Nov; 122(22):2691-4. PubMed ID: 19951597
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
