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Volumn 13, Issue 1, 2007, Pages 162-164

Ophthalmic surgery in prion diseases

Author keywords

[No Author keywords available]

Indexed keywords

PRION PROTEIN;

EID: 33846093065     PISSN: 10806040     EISSN: 10806059     Source Type: Journal    
DOI: 10.3201/eid1301.061004     Document Type: Article
Times cited : (12)

References (15)
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    • Lueck, C.J.1    McIlwain, G.G.2    Zeidler, M.3
  • 3
    • 27744473803 scopus 로고    scopus 로고
    • Isolated visual symptoms at onset in sporadic Creutzfeldt-Jakob disease: The clinical phenotype of the Heidenhain variant
    • Cooper SA, Murray KL, Heath CA, Will RG, Knight RSG. Isolated visual symptoms at onset in sporadic Creutzfeldt-Jakob disease: the clinical phenotype of the "Heidenhain variant." Br J Ophthalmol. 2005;89:1341-2.
    • (2005) Br J Ophthalmol , vol.89 , pp. 1341-1342
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  • 4
    • 0037386383 scopus 로고    scopus 로고
    • Creutzfeldt-Jakob disease and eye surgery - new disease, old disease
    • Tullo A. Creutzfeldt-Jakob disease and eye surgery - new disease, old disease. J Cataract Refract Surg. 2003;29:629-31.
    • (2003) J Cataract Refract Surg , vol.29 , pp. 629-631
    • Tullo, A.1
  • 6
    • 24044500298 scopus 로고    scopus 로고
    • Abnormal prion protein in the retina of the most commonly occurring subtype of sporadic Creutzfeldt-Jakob disease
    • Head MW, Peden AH, Yull HM, Ritchie DL, Bonshek RE, Tullo AB, et al. Abnormal prion protein in the retina of the most commonly occurring subtype of sporadic Creutzfeldt-Jakob disease. Br J Ophthalmol. 2005;89:1131-3.
    • (2005) Br J Ophthalmol , vol.89 , pp. 1131-1133
    • Head, M.W.1    Peden, A.H.2    Yull, H.M.3    Ritchie, D.L.4    Bonshek, R.E.5    Tullo, A.B.6
  • 9
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    • (1999) Report of a WHO consultation
  • 10
    • 0018360851 scopus 로고
    • Creutzfeldt-Jakob disease: Patterns of worldwide occurrence and the significance of familial and sporadic clustering
    • Masters CL, Harris JO, Gajdusek DC, Gibbs CJ Jr, Bernoulli C, Asher DM. Creutzfeldt-Jakob disease: patterns of worldwide occurrence and the significance of familial and sporadic clustering. Ann Neurol. 1979;5:177-88.
    • (1979) Ann Neurol , vol.5 , pp. 177-188
    • Masters, C.L.1    Harris, J.O.2    Gajdusek, D.C.3    Gibbs Jr, C.J.4    Bernoulli, C.5    Asher, D.M.6
  • 11
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    • World Health Organization (WHO). The revision of the variant Creutzfeldt-Jakob (vCJD) case definition. Report of a WHO consultation. Edinburgh, United Kingdom, 2001 17 May (WHO/CDS/CSR/EPH/2001.5). Geneva: WHO; 2001.
  • 12
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    • Inactivation of transmissible degenerative encephalopathy agents: A review
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    • Vision change and quality of life in the elderly. Response to cataract surgery and treatment of other chronic ocular conditions
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.