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BMJ Case Reports
Volumn , Issue , 2009, Pages
Familial Creutzfeldt-Jakob disease with E200K mutation presenting with neurosensorial hypoacusis
Author keywords

[No Author keywords available]
Indexed keywords

EID: 84896534723     PISSN: None     EISSN: 1757790X     Source Type: Journal    
DOI: 10.1136/bcr.06.2009.2006     Document Type: Article
Times cited : (3)
References (5)
  • 1
    • 24944561061 scopus 로고    scopus 로고
    • Prion diseases
    • DOI 10.1016/S1474-4422(05)70192-7, PII S1474442205701927
    • Johnson RT. Prion diseases. Lancet Neurol 2005; 4: 635-42. [CrossRef ] [Medline] [Web of Science] (Pubitemid 41317298)
    • (2005) Lancet Neurology , vol.4 , Issue.10 , pp. 635-642
    • Johnson, R.T.1
  • 2
    • 0031747398 scopus 로고    scopus 로고
    • Otolary ngological manif estations of Creutzfeldt-Jakob disease
    • [Medline] [Web of Science]
    • Bigelow DC, Eisen MD, Yen DM, et al. Otolary ngological manif estations of Creutzfeldt-Jakob disease. Arch Otolaryngol Head Neck Surg 1998; 124: 707-10. [Medline] [Web of Science]
    • (1998) Arch Otolaryngol Head Neck Surg , vol.124 , pp. 707-710
    • Bigelow, D.C.1    Eisen, M.D.2    Yen, D.M.3
  • 3
    • 0034137786 scopus 로고    scopus 로고
    • Deafness: An unusual onset of genetic Creutzfeldt-Jakob disease
    • [CrossRef ] [Medline] [Web of Science]
    • Cataldi ML, Restivo O, Reggio E, et al. Deafness: an unusual onset of genetic Creutzfeldt-Jakob disease. Neurol Sci 2000; 21: 53-5. [CrossRef ] [Medline] [Web of Science]
    • (2000) Neurol Sci , vol.21 , pp. 53-55
    • Cataldi, M.L.1    Restivo, O.2    Reggio, E.3
  • 4
    • 22144485913 scopus 로고    scopus 로고
    • Neuropathologic characteristics of brainstem lesions in sporadic Creutzfeldt-Jakob disease
    • DOI 10.1007/s00401-005-0981-0
    • Iwasaki Y, Hashizume Y, Yoshida M, et al. Neuropathologic characteristics of brainstem lesions in sporadic Creutzfeldt-Jakob disease. Acta Neuropathol 2005; 109: 557-66. [CrossRef ] [Medline] (Pubitemid 40974144)
    • (2005) Acta Neuropathologica , vol.109 , Issue.6 , pp. 557-566
    • Iwasaki, Y.1    Hashizume, Y.2    Yoshida, M.3    Kitamoto, T.4    Sobue, G.5
  • 5
    • 0032975733 scopus 로고    scopus 로고
    • A novel phenotype in familial Creutzfeldt-Jakob disease: Prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease- resistant prion protein
    • DOI 10.1002/1531-8249(199906)45:6<812::AID-ANA20
    • Hainfellner JA, Parchi P, Kitamoto T, et al. A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type-2 protease-resistant prion protein. Ann Neurol 1999; 45: 812-16. [CrossRef ] [Medline] [Web of Science] (Pubitemid 29260763)
    • (1999) Annals of Neurology , vol.45 , Issue.6 , pp. 812-816
    • Hainfellner, J.A.1    Parchi, P.2    Kitamoto, T.3    Jarius, C.4    Gambetti, P.5    Budka, H.6

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.