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Volumn 277, Issue 1-2, 2009, Pages 119-123

Clinical diagnosis of Creutzfeldt-Jakob disease: Accuracy based on analysis of autopsy-confirmed cases

Author keywords

Cerebrospinal fluid; Clinical diagnosis; Creutzfeldt Jakob disease; Diagnostic criteria; Magnetic resonance imaging; Myoclonus; Periodic sharp wave complexes

Indexed keywords

ADULT; AGED; ARTICLE; AUTOPSY; CLINICAL EXAMINATION; CONSCIOUSNESS; CONTROLLED STUDY; CREUTZFELDT JAKOB DISEASE; DEMENTIA; DIAGNOSTIC ACCURACY; DIAGNOSTIC ERROR; DISEASE COURSE; FEMALE; HUMAN; LABORATORY TEST; MALE; MYOCLONUS; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOLOGY; PRIORITY JOURNAL; RETROSPECTIVE STUDY;

EID: 58149279288     PISSN: 0022510X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jns.2008.10.026     Document Type: Article
Times cited : (33)

References (21)
  • 2
    • 0032585594 scopus 로고    scopus 로고
    • Creutzfeldt-Jakob disease and related transmissible spongiform encephalopathies
    • Johnson R.T., and Gibbs Jr. C.J. Creutzfeldt-Jakob disease and related transmissible spongiform encephalopathies. N Engl J Med 339 (1998) 1994-2004
    • (1998) N Engl J Med , vol.339 , pp. 1994-2004
    • Johnson, R.T.1    Gibbs Jr., C.J.2
  • 3
    • 0033844156 scopus 로고    scopus 로고
    • Current clinical diagnosis in Creutzfeldt-Jakob disease: identification of uncommon variants
    • Zerr I., Schulz-Schaeffer W.J., Giese A., Bodemer M., Schröter A., Henkel K., et al. Current clinical diagnosis in Creutzfeldt-Jakob disease: identification of uncommon variants. Ann Neurol 48 (2000) 323-329
    • (2000) Ann Neurol , vol.48 , pp. 323-329
    • Zerr, I.1    Schulz-Schaeffer, W.J.2    Giese, A.3    Bodemer, M.4    Schröter, A.5    Henkel, K.6
  • 6
    • 33644840505 scopus 로고    scopus 로고
    • Creutzfeldt-Jakob Disease Surveillance Committee, Japan. The first Japanese case of variant Creutzfeldt-Jakob disease showing periodic electroencephalogram
    • Variant CJD Working Group
    • Yamada M., and Variant CJD Working Group. Creutzfeldt-Jakob Disease Surveillance Committee, Japan. The first Japanese case of variant Creutzfeldt-Jakob disease showing periodic electroencephalogram. Lancet 367 (2006) 874
    • (2006) Lancet , vol.367 , pp. 874
    • Yamada, M.1
  • 7
    • 0028876473 scopus 로고
    • Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases)
    • Budka H., Aguzzi A., Brown P., Brucher J.M., Bugiani O., Gullotta F., et al. Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases). Brain Pathol 5 (1995) 459-466
    • (1995) Brain Pathol , vol.5 , pp. 459-466
    • Budka, H.1    Aguzzi, A.2    Brown, P.3    Brucher, J.M.4    Bugiani, O.5    Gullotta, F.6
  • 10
    • 33749663648 scopus 로고    scopus 로고
    • Clinicopathologic characteristics of sporadic Japanese Creutzfeldt-Jakob disease classified according to prion protein gene polymorphism and prion protein type
    • Iwasaki Y., Yoshida M., Hashizume Y., Kitamoto T., and Sobue G. Clinicopathologic characteristics of sporadic Japanese Creutzfeldt-Jakob disease classified according to prion protein gene polymorphism and prion protein type. Acta Neuropathol (Berl) 112 (2006) 561-571
    • (2006) Acta Neuropathol (Berl) , vol.112 , pp. 561-571
    • Iwasaki, Y.1    Yoshida, M.2    Hashizume, Y.3    Kitamoto, T.4    Sobue, G.5
  • 11
    • 0032816292 scopus 로고    scopus 로고
    • Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects
    • Parchi P., Giese A., Capellari S., Brown P., Schulz-Schaeffer W., Windl O., et al. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects. Ann Neurol 46 (1999) 224-233
    • (1999) Ann Neurol , vol.46 , pp. 224-233
    • Parchi, P.1    Giese, A.2    Capellari, S.3    Brown, P.4    Schulz-Schaeffer, W.5    Windl, O.6
  • 12
    • 0032726890 scopus 로고    scopus 로고
    • Clinicopathological characteristics of Creutzfeldt-Jakob disease with a PrP V180I mutation and M129 V polymorphism on different alleles
    • (in Japanese with English abstract)
    • Iwasaki Y., Sone M., Kato T., Yoshida E., Indo T., Yoshida M., et al. Clinicopathological characteristics of Creutzfeldt-Jakob disease with a PrP V180I mutation and M129 V polymorphism on different alleles. Rinsho Shinkeigaku 39 (1999) 800-806 (in Japanese with English abstract)
    • (1999) Rinsho Shinkeigaku , vol.39 , pp. 800-806
    • Iwasaki, Y.1    Sone, M.2    Kato, T.3    Yoshida, E.4    Indo, T.5    Yoshida, M.6
  • 14
    • 22144478434 scopus 로고    scopus 로고
    • An autopsy case of severe autonomic failure with Parkinson's disease associated with Creutzfeldt-Jakob disease
    • Watanabe H., Hamada K., Hishikawa N., Iwasaki Y., Ito H., Hirayama M., et al. An autopsy case of severe autonomic failure with Parkinson's disease associated with Creutzfeldt-Jakob disease. Neuropathology 23 (2003) A42
    • (2003) Neuropathology , vol.23
    • Watanabe, H.1    Hamada, K.2    Hishikawa, N.3    Iwasaki, Y.4    Ito, H.5    Hirayama, M.6
  • 15
    • 1042288147 scopus 로고    scopus 로고
    • Clinical features of Creutzfeldt-Jakob disease with V180I mutation
    • Jin K., Shiga Y., Shibuya S., Chida K., Sato Y., Konno H., et al. Clinical features of Creutzfeldt-Jakob disease with V180I mutation. Neurology 62 (2004) 502-505
    • (2004) Neurology , vol.62 , pp. 502-505
    • Jin, K.1    Shiga, Y.2    Shibuya, S.3    Chida, K.4    Sato, Y.5    Konno, H.6
  • 17
  • 18
    • 33751266274 scopus 로고    scopus 로고
    • Autopsy case of sporadic Creutzfeldt-Jakob disease presenting with signs suggestive of brainstem and spinal cord involvement
    • Iwasaki Y., Iijima M., Kimura S., Yoshida M., Hashizume Y., Yamada M., et al. Autopsy case of sporadic Creutzfeldt-Jakob disease presenting with signs suggestive of brainstem and spinal cord involvement. Neuropathology 26 (2006) 550-556
    • (2006) Neuropathology , vol.26 , pp. 550-556
    • Iwasaki, Y.1    Iijima, M.2    Kimura, S.3    Yoshida, M.4    Hashizume, Y.5    Yamada, M.6
  • 19
    • 3543049532 scopus 로고    scopus 로고
    • Sensitivity of 14-3-3 protein test varies in subtypes of sporadic Creutzfeldt-Jakob disease
    • Castellani R.J., Colucci M., Xie Z., Zou W., Li C., Parchi P., et al. Sensitivity of 14-3-3 protein test varies in subtypes of sporadic Creutzfeldt-Jakob disease. Neurology 63 (2004) 436-442
    • (2004) Neurology , vol.63 , pp. 436-442
    • Castellani, R.J.1    Colucci, M.2    Xie, Z.3    Zou, W.4    Li, C.5    Parchi, P.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.