These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

464 related items for PubMed ID: 17317389

  • 1. 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; 143(3):416-9. PubMed ID: 17317389
    [Abstract] [Full Text] [Related]

  • 2. Deposits of transforming growth factor-beta-induced protein in granular corneal dystrophy type II after LASIK.
    Kim TI, Roh MI, Grossniklaus HE, Kang SJ, Hamilton SM, Schorderet DF, Lee WB, Kim EK.
    Cornea; 2008 Jan; 27(1):28-32. PubMed ID: 18245963
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. Avellino corneal dystrophy after LASIK.
    Jun RM, Tchah H, Kim TI, Stulting RD, Jung SE, Seo KY, Lee DH, Kim EK.
    Ophthalmology; 2004 Mar; 111(3):463-8. PubMed ID: 15019320
    [Abstract] [Full Text] [Related]

  • 6. Outcome of LASIK in fleck corneal dystrophy.
    Banning CS, Larson PM, Randleman JB.
    Cornea; 2006 Dec; 25(10):1262-4. PubMed ID: 17172916
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. 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 18; 13():1976-83. PubMed ID: 17982422
    [Abstract] [Full Text] [Related]

  • 10. 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 18; 138(5):772-81. PubMed ID: 15531312
    [Abstract] [Full Text] [Related]

  • 11. Lattice corneal dystrophy type I without typical lattice lines: role of mutational analysis.
    Yoshida S, Yoshida A, Nakao S, Emori A, Nakamura T, Fujisawa K, Kumano Y, Ishibashi T.
    Am J Ophthalmol; 2004 Mar 18; 137(3):586-8. PubMed ID: 15013897
    [Abstract] [Full Text] [Related]

  • 12. LASIK surgery of granular corneal dystrophy type 2 patients leads to accumulation and differential proteolytic processing of transforming growth factor beta-induced protein (TGFBIp).
    Poulsen ET, Nielsen NS, Jensen MM, Nielsen E, Hjortdal J, Kim EK, Enghild JJ.
    Proteomics; 2016 Feb 18; 16(3):539-43. PubMed ID: 26864644
    [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 10; 12():331-5. PubMed ID: 16636649
    [Abstract] [Full Text] [Related]

  • 14. Laser in situ keratomileusis in a patient with presumed central cloudy corneal dystrophy of Francois.
    Zaidi A, McLeod SD.
    Am J Ophthalmol; 2005 Feb 10; 139(2):376-7. PubMed ID: 15734014
    [Abstract] [Full Text] [Related]

  • 15. 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
    [Abstract] [Full Text] [Related]

  • 16. Granular and lattice deposits in corneal dystrophy caused by R124C mutation of TGFBIp.
    Patel DA, Chang SH, Harocopos GJ, Vora SC, Thang DH, Huang AJ.
    Cornea; 2010 Nov 27; 29(11):1215-22. PubMed ID: 20697279
    [Abstract] [Full Text] [Related]

  • 17. 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
    [Abstract] [Full Text] [Related]

  • 18. Histopathologic study of corneal stromal dystrophies: a 10-year experience.
    Santos LN, Fernandes BF, de Moura LR, Cheema DP, Maloney S, Logan P, Burnier MN.
    Cornea; 2007 Oct 17; 26(9):1027-31. PubMed ID: 17893527
    [Abstract] [Full Text] [Related]

  • 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 17; 111(7):1407-9. PubMed ID: 15234146
    [Abstract] [Full Text] [Related]

  • 20. New histopathologic and ultrastructural findings in Reis-Bücklers corneal dystrophy caused by the Arg124Leu mutation of TGFBI gene.
    Qiu WY, Zheng LB, Pan F, Wang BB, Yao YF.
    BMC Ophthalmol; 2016 Sep 02; 16(1):158. PubMed ID: 27590038
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 24.