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Volumn 225, Issue 7, 2008, Pages 616-622

New international classification of corneal dystrophies and clinical landmarks;Neue internationale klassifikation der hornhautdystrophien und klinische "Schlüsselbefunde"

Author keywords

Clinical "landmarks"; Corneal Dystrophies; International Committee; New classification; Supplement publication "Cornea"

Indexed keywords

CORNEA DYSTROPHY; CORNEA OPACITY; DISEASE CLASSIFICATION; GENETICS; HISTOLOGY; HUMAN; OPHTHALMOLOGY; REVIEW;

EID: 50149115156     PISSN: 00232165     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2008-1027552     Document Type: Review
Times cited : (8)

References (13)
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  • 3
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  • 4
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    • GK, K.1
  • 6
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    • The classic form of granular corneal dystrophy associated with R555W mutation in the BigH3 gene is rare in Japanese patients
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  • 8
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    • Kerato-epithelin mutations in four 5q31 linked corneal dystrophies
    • Munier FL, Korvatska E, Djemai A et al. Kerato-epithelin mutations in four 5q31 linked corneal dystrophies. Nat Genet 1997; 15: 247-251
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  • 9
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    • A new X-linked endothelial corneal dystrophy
    • Schmid E, Lisch W, Philipp W et al. A new X-linked endothelial corneal dystrophy. Am J Ophthalmol 2006; 141: 478-487
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    • Schmid, E.1    Lisch, W.2    Philipp, W.3
  • 11
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    • Die wabenförmige Hornhautdystrophie (Thiel-Behnke). Neubewertung und Abgrenzung gegenüber der Reis-Bücklersschen Hornhautdystrophie.
    • Weidle EG. Die wabenförmige Hornhautdystrophie (Thiel-Behnke). Neubewertung und Abgrenzung gegenüber der Reis-Bücklersschen Hornhautdystrophie. Klin Monatsbl Augenheilkd 1999; 214: 125-135
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    • Mutations in the UBIAD1 gene on chromosome short arm 1, region 36 cause Schnyder crystalline corneal dystrophy
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.