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Volumn 224, Issue 10, 2007, Pages 791-793

Unilateral pigmented paravenous retinochoroidal atrophy;Unilaterale pigmentierte paravenöse retinochorioidale atrophie

Author keywords

Angiography; Autofluorescence; Electrophysiology; Pigmented paravenous retinochoroidal atrophy; Retina; Unilateral

Indexed keywords

ADULT; BRAIN ELECTROPHYSIOLOGY; CASE REPORT; CENTRAL SCOTOMA; CHORIORETINOPATHY; CLINICAL FEATURE; ELECTROOCULOGRAPHY; ELECTRORETINOGRAM; HUMAN; OPHTHALMOSCOPY; PERIMETRY; PIGMENT EPITHELIUM; RETINA DISEASE; RETINA DYSTROPHY; RETINOCHOROID ATROPHY; SHORT SURVEY; VISUAL ACUITY;

EID: 35948976926     PISSN: 00232165     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-963600     Document Type: Short Survey
Times cited : (13)

References (10)
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  • 2
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  • 3
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    • Sopra un caso di pigmentazione anomala di fondo oculare (mellanosi della retina)
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  • 4
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    • Retinal choroiditis radiate
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  • 7
    • 18144439528 scopus 로고    scopus 로고
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    • Kukner AS, Yilmaz T, Celebi S et al. Pigmented paravenous retinochoroidal atrophy. A literature review supported by seven cases. Ophthalmologica 2003; 217: 436-440
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  • 8
    • 11144269802 scopus 로고    scopus 로고
    • Pigmented paravenous chorioretinal atrophy is associated with a mutation within the crumbs homolog 1 (CRB1) gene
    • McKay GJ, Clarke S, Davis JA et al. Pigmented paravenous chorioretinal atrophy is associated with a mutation within the crumbs homolog 1 (CRB1) gene. Invest Ophthalmol Vis Sci 2005; 46: 322-328
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.