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Ophthalmology
Volumn 120, Issue 1, 2013, Pages 215-216
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Author keywords

[No Author keywords available]
Indexed keywords

CONGENITAL CORNEA DYSTROPHY; CORNEA DYSTROPHY; DESCEMET STRIPPING ENDOTHELIAL KERATOPLASTY; GENETIC SCREENING; HUMAN; LETTER; POSTERIOR POLYMORPHOUS DYSTROPHY; PRIORITY JOURNAL; PROGNOSIS; TREATMENT OUTCOME; VISUAL ACUITY; CORNEA EDEMA; FEMALE; METHODOLOGY; NOTE; VISUAL DISORDER;
EID: 84872016037     PISSN: 01616420     EISSN: 15494713     Source Type: Journal    
DOI: 10.1016/j.ophtha.2012.08.038     Document Type: Letter
Times cited : (9)
References (5)
  • 1
    • 67650421522 scopus 로고    scopus 로고
    • Spontaneous corneal clearance despite graft detachment in Descemet membrane endothelial keratoplasty
    • C. Balachandran, L. Ham, C.A. Verschoor Spontaneous corneal clearance despite graft detachment in Descemet membrane endothelial keratoplasty Am J Ophthalmol 148 2009 227 234
    • (2009) Am J Ophthalmol , vol.148 , pp. 227-234
    • Balachandran, C.1    Ham, L.2    Verschoor, C.A.3
  • 2
    • 84856532089 scopus 로고    scopus 로고
    • Spontaneous corneal clearing after Descemet's stripping without endothelial replacement
    • R.D. Shah, J.B. Randleman, H.E. Grossnikalus Spontaneous corneal clearing after Descemet's stripping without endothelial replacement Ophthalmology 119 2012 256 260
    • (2012) Ophthalmology , vol.119 , pp. 256-260
    • Shah, R.D.1    Randleman, J.B.2    Grossnikalus, H.E.3
  • 3
    • 22144445323 scopus 로고    scopus 로고
    • Inheritance of a novel COL8A2 mutation defines a distinct early-onset subtype of Fuchs corneal dystrophy
    • J.D. Gottsch, O.H. Sundin, S.H. Liu Inheritance of a novel COL8A2 mutation defines a distinct early-onset subtype of Fuchs corneal dystrophy Invest Ophthalmol Vis Sci 46 2005 1934 1939
    • (2005) Invest Ophthalmol Vis Sci , vol.46 , pp. 1934-1939
    • Gottsch, J.D.1    Sundin, O.H.2    Liu, S.H.3
  • 4
    • 84855916773 scopus 로고    scopus 로고
    • A cellular model for the investigation of Fuchs' endothelial corneal dystrophy
    • C. Kelliher, S. Chakravarti, N. Vij A cellular model for the investigation of Fuchs' endothelial corneal dystrophy Exp Eye Res 93 2011 880 888
    • (2011) Exp Eye Res , vol.93 , pp. 880-888
    • Kelliher, C.1    Chakravarti, S.2    Vij, N.3
  • 5
    • 84856494249 scopus 로고    scopus 로고
    • A multicenter study to map genes for Fuchs endothelial corneal dystrophy: Baseline characteristics and heritability
    • FECD Genetics Multi-Center Study Group
    • M.D. Louttit, L.J. Kopplin, R.P. Igo Jr FECD Genetics Multi-Center Study Group A multicenter study to map genes for Fuchs endothelial corneal dystrophy: baseline characteristics and heritability Cornea 31 2012 26 35
    • (2012) Cornea , vol.31 , pp. 26-35
    • Louttit, M.D.1    Kopplin, L.J.2    Igo, Jr.R.P.3

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.