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Volumn 122, Issue 3, 1996, Pages 382-392

Pattern dystrophy of the retinal pigment epithelium and geographic atrophy of the macula

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; CASE REPORT; CHOROID CAPILLARY LAYER; ELECTROOCULOGRAM; ELECTRORETINOGRAPHY; GEOGRAPHY; HUMAN; PIGMENT EPITHELIUM; PRIORITY JOURNAL; RETINA DYSTROPHY; RETINA MACULA DEGENERATION; SCOTOMA; VISUAL IMPAIRMENT;

EID: 0029781852     PISSN: 00029394     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9394(14)72065-3     Document Type: Article
Times cited : (45)

References (18)
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    • Pattern dystrophy of the pigment epithelium
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  • 2
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    • Patterned dystrophies of the retinal pigment epithelium
    • Hsieh RC Fine BS Lyons JS Patterned dystrophies of the retinal pigment epithelium Arch Ophthalmol 95 1977 429 435
    • (1977) Arch Ophthalmol , vol.95 , pp. 429-435
    • Hsieh, RC1    Fine, BS2    Lyons, JS3
  • 3
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    • Autosomal dominant dystrophy of the retinal pigment epithelium
    • O'Donnell FE Schatz H Reid P Green WR Autosomal dominant dystrophy of the retinal pigment epithelium Arch Ophthalmol 97 1979 680 683
    • (1979) Arch Ophthalmol , vol.97 , pp. 680-683
    • O'Donnell, FE1    Schatz, H2    Reid, P3    Green, WR4
  • 4
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    • Butterfly-shaped macular dystrophy in four generations
    • Prensky JG Bresnick GH Butterfly-shaped macular dystrophy in four generations Arch Ophthalmol 101 1983 1198 1203
    • (1983) Arch Ophthalmol , vol.101 , pp. 1198-1203
    • Prensky, JG1    Bresnick, GH2
  • 5
  • 7
    • 85114547523 scopus 로고
    • Munteanu GH Distrofiile Retinei si Corodei 1985 Editura Facia Timisoara, Romania
    • (1985)
    • Munteanu, GH1
  • 9
    • 0019978528 scopus 로고
    • Pigment epithelial pattern dystrophy
    • deJong PTVM Delleman JW Pigment epithelial pattern dystrophy Arch Ophthalmol 100 1982 1416 1421
    • (1982) Arch Ophthalmol , vol.100 , pp. 1416-1421
    • deJong, PTVM1    Delleman, JW2
  • 10
    • 85114534353 scopus 로고    scopus 로고
    • Marmor MF, Zrenner E, for the International Society for Clinical Electrophysiology of Vision. Standard for clinical electroretinography. 1994 Update. Doc Ophthalmol 1995;89:199–210
  • 11
    • 0017407604 scopus 로고
    • Fundus albipunctatus: a clinical study of the fundus lesions, the physiologic deficit, and the vitamin A metabolism
    • Marmor MF Fundus albipunctatus: a clinical study of the fundus lesions, the physiologic deficit, and the vitamin A metabolism Doc Ophthalmol 43 1977 277 302
    • (1977) Doc Ophthalmol , vol.43 , pp. 277-302
    • Marmor, MF1
  • 12
    • 85114534809 scopus 로고    scopus 로고
    • Marmor MF, Zrenner E (for the International Society for Clinical Electrophysiology of Vision). Standard for clinical electro-oculography. Arch Ophthalmol 1993;111:601–4
  • 13
    • 0027401094 scopus 로고
    • Butterfly-shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene
    • Nichols BE Sheffield VC Vandenburgh K Drack AV Kimura AE Stone EM Butterfly-shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene Nat Genet 3 1993 202 207
    • (1993) Nat Genet , vol.3 , pp. 202-207
    • Nichols, BE1    Sheffield, VC2    Vandenburgh, K3    Drack, AV4    Kimura, AE5    Stone, EM6
  • 14
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    • Identification of rhodopsin gene mutations using GC-clamped denaturing gradient gel electrophoresis
    • Stone EM Vandenburgh K Nichols BE Sheffield VC Identification of rhodopsin gene mutations using GC-clamped denaturing gradient gel electrophoresis Methods Neurosci 15 1993 377 391
    • (1993) Methods Neurosci , vol.15 , pp. 377-391
    • Stone, EM1    Vandenburgh, K2    Nichols, BE3    Sheffield, VC4
  • 15
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    • Refining the locus for Best vitelliform macular dystrophy and mutation analysis of the candidate gene ROM-1
    • Nichols BE Bascom R Litt M McInnes R Sheffield VC Stone EM Refining the locus for Best vitelliform macular dystrophy and mutation analysis of the candidate gene ROM-1 Am J Hum Genet 54 1994 95 103
    • (1994) Am J Hum Genet , vol.54 , pp. 95-103
    • Nichols, BE1    Bascom, R2    Litt, M3    McInnes, R4    Sheffield, VC5    Stone, EM6
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  • 17
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    • Clinical features of a previously undescribed codon (proline to serine) mutation in the peripherin/retinal degeneration slow gene in autosomal dominant retinitis pigmentosa
    • Fishman GA Stone E Gilbert LD Vandenburgh K Sheffield VC Heckenlively JR Clinical features of a previously undescribed codon (proline to serine) mutation in the peripherin/retinal degeneration slow gene in autosomal dominant retinitis pigmentosa Ophthalmology 101 1994 1409 1421
    • (1994) Ophthalmology , vol.101 , pp. 1409-1421
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.