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Journal Abstract Search

200 related items for PubMed ID: 16541014

  • 1. Unilateral lattice corneal dystrophy associated with the novel His572del mutation in the TGFBI gene.
    Aldave AJ, Rayner SA, Kim BT, Prechanond A, Yellore VS.
    Mol Vis; 2006 Feb 27; 12():142-6. PubMed ID: 16541014
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  • 4. 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 27; 144(3):473-5. PubMed ID: 17765440
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  • 7. 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 27; 46(1):121-5. PubMed ID: 15623763
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  • 8. 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 27; 138(5):772-81. PubMed ID: 15531312
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  • 9. The TGFBI A546D mutation causes an atypical type of lattice corneal dystrophy.
    Correa-Gomez V, Villalvazo-Cordero L, Zenteno JC.
    Mol Vis; 2007 Sep 17; 13():1695-700. PubMed ID: 17893671
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  • 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 Sep 17; 40(2):105-8. PubMed ID: 18259096
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  • 12. 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 17; 93(7):932-7. PubMed ID: 19001012
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  • 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 10; 12():331-5. PubMed ID: 16636649
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  • 14. 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 10; 33(3):294-9. PubMed ID: 24473223
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  • 15. 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 10; 46(4):1133-9. PubMed ID: 15790870
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  • 16. 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 10; 116(1):46-51. PubMed ID: 19019446
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  • 17. A clinical and histopathologic examination of accelerated TGFBIp deposition after LASIK in combined granular-lattice corneal dystrophy.
    Aldave AJ, Sonmez B, Forstot SL, Rayner SA, Yellore VS, Glasgow BJ.
    Am J Ophthalmol; 2007 Mar 10; 143(3):416-9. PubMed ID: 17317389
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  • 18. 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 10; 21(5):587-90. PubMed ID: 16440005
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  • 19. The usefulness of buccal swabs for mutation screening in patients with suspected corneal dystrophies.
    Aldave AJ, Yellore VS, Self CA, Holsclaw D, Small K.
    Ophthalmology; 2004 Jul 10; 111(7):1407-9. PubMed ID: 15234146
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  • 20. [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 10; 23(3):310-2. PubMed ID: 16767671
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