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Volumn 21, Issue 8, 2006, Pages 395-399

Prion diseases;Enfermedades priónicas o prionpatías

Author keywords

Creutzfeldt Jakob disease; Prion; Spongiform encephalopathies

Indexed keywords

ANIMAL; CLASSIFICATION; EDITORIAL; EUROPE; HEALTH SURVEY; HUMAN; PATHOPHYSIOLOGY; PRION DISEASE;

EID: 39049190586     PISSN: 02134853     EISSN: 15781968     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (4)

References (41)
  • 1
    • 39049181466 scopus 로고    scopus 로고
    • Neuroimagen en el diagnóstico de las encefalopatías espongiformes transmisibles humanas.
    • Moreno Izco F, Arriola Larrarte L. Neuroimagen en el diagnóstico de las encefalopatías espongiformes transmisibles humanas. Neurología 2006;21:428-36.
    • (2006) Neurología , vol.21 , pp. 428-436
    • Moreno Izco, F.1    Arriola Larrarte, L.2
  • 2
    • 39049184780 scopus 로고    scopus 로고
    • Enfermedad de Creutzfeldt-Jakob esporádica, variante MM1, asociada a mutismo acinético de larga duración.
    • Sánchez-Valle R, Santamaría J, Rey MJ, Rodríguez A, Graus F, Saiz A. Enfermedad de Creutzfeldt-Jakob esporádica, variante MM1, asociada a mutismo acinético de larga duración. Neurología 2006;21:444-6.
    • (2006) Neurología , vol.21 , pp. 444-446
    • Sánchez-Valle, R.1    Santamaría, J.2    Rey, M.J.3    Rodríguez, A.4    Graus, F.5    Saiz, A.6
  • 3
    • 39049177807 scopus 로고    scopus 로고
    • Evolución clínicorradiológica atípica en un caso de variante encefalopática de la enfermedad de Creutzfeldt-Jakob.
    • Pascual Lozano AM, Salvador Aliaga A, Coret Ferrer F, Láinez Andrés JM. Evolución clínicorradiológica atípica en un caso de variante encefalopática de la enfermedad de Creutzfeldt-Jakob. Neurología 2006;21:439-43.
    • (2006) Neurología , vol.21 , pp. 439-443
    • Pascual Lozano, A.M.1    Salvador Aliaga, A.2    Coret Ferrer, F.3    Láinez Andrés, J.M.4
  • 4
    • 39049195249 scopus 로고    scopus 로고
    • Neuroimagen en la enfermedad de Creutzfeldt-Jakob.
    • Riverol M, Arbizu J, Luquin MR. Neuroimagen en la enfermedad de Creutzfeldt-Jakob. Neurología 2006;21:437-8.
    • (2006) Neurología , vol.21 , pp. 437-438
    • Riverol, M.1    Arbizu, J.2    Luquin, M.R.3
  • 6
    • 0347915581 scopus 로고    scopus 로고
    • Transmissible spongiform encephalopathies
    • Collins SJ, Lawson VA, Masters CL. Transmissible spongiform encephalopathies. Lancet 2004;363:51-61.
    • (2004) Lancet , vol.363 , pp. 51-61
    • Collins, S.J.1    Lawson, V.A.2    Masters, C.L.3
  • 7
    • 21344445937 scopus 로고    scopus 로고
    • Molecular neurology of prion diseases
    • Collinge J. Molecular neurology of prion diseases. J Neurol Neurosurg Psychiatry 2005;76:906-19.
    • (2005) J Neurol Neurosurg Psychiatry , vol.76 , pp. 906-919
    • Collinge, J.1
  • 8
    • 0035902194 scopus 로고    scopus 로고
    • Shattuck lecture-neurodegenerative diseases and prions
    • Prusiner SB. Shattuck lecture-neurodegenerative diseases and prions. N Engl J Med 2001;344:1516-26.
    • (2001) N Engl J Med , vol.344 , pp. 1516-1526
    • Prusiner, S.B.1
  • 10
    • 0038668790 scopus 로고    scopus 로고
    • Prion diseases. Cannibals and garbage piles
    • Aguzzi A, Heikenwalder M. Prion diseases. Cannibals and garbage piles. Nature 2003;423:127-28.
    • (2003) Nature , vol.423 , pp. 127-128
    • Aguzzi, A.1    Heikenwalder, M.2
  • 11
    • 0016732842 scopus 로고
    • Epidemiology of Creutzfeldt-Jakob Disease in England and Wales
    • Matthews WB. Epidemiology of Creutzfeldt-Jakob Disease in England and Wales, J Neurol Neurosurg Psychiatry 1975;38:210-3.
    • (1975) J Neurol Neurosurg Psychiatry , vol.38 , pp. 210-213
    • Matthews, W.B.1
  • 12
    • 0018599223 scopus 로고
    • Creutzfeldt-Jakob disease in France: III. Epidemiological study of 170 patients dying during the decade 1968-1977
    • Brown P, Cathala F, Gajdusek DC. Creutzfeldt-Jakob disease in France: III. Epidemiological study of 170 patients dying during the decade 1968-1977. Ann Neurol 1979;6:438-46.
    • (1979) Ann Neurol , vol.6 , pp. 438-446
    • Brown, P.1    Cathala, F.2    Gajdusek, D.C.3
  • 13
    • 0023243707 scopus 로고
    • The epidemiology of Creutzfeldt-Jakob disease: Conclusion of a 15-year investigation in France and review of the world literature
    • Brown P, Cathala F, Raubertas RF, Gajdusek DC, Castaigne P. The epidemiology of Creutzfeldt-Jakob disease: conclusion of a 15-year investigation in France and review of the world literature. Neurology 1987;37:895-904.
    • (1987) Neurology , vol.37 , pp. 895-904
    • Brown, P.1    Cathala, F.2    Raubertas, R.F.3    Gajdusek, D.C.4    Castaigne, P.5
  • 14
    • 33747040538 scopus 로고    scopus 로고
    • Iatrogenic Creutzfeldt-Jakob disease. The waning of an era
    • Brown P, Brandel JP, Preese M, Sato T. Iatrogenic Creutzfeldt-Jakob disease. The waning of an era. Neurology 2006;67:389-93.
    • (2006) Neurology , vol.67 , pp. 389-393
    • Brown, P.1    Brandel, J.P.2    Preese, M.3    Sato, T.4
  • 15
    • 1142273431 scopus 로고    scopus 로고
    • Possible transmission of variant Creutzfeldt Jakob disease by blood transfusion
    • Llewelyn CA, Hewitt PE, Knight RS, Amar K, Cousens S, Mackenzie J, et al. Possible transmission of variant Creutzfeldt Jakob disease by blood transfusion. Lancet 2004;363:417-21.
    • (2004) Lancet , vol.363 , pp. 417-421
    • Llewelyn, C.A.1    Hewitt, P.E.2    Knight, R.S.3    Amar, K.4    Cousens, S.5    Mackenzie, J.6
  • 16
    • 4043157677 scopus 로고    scopus 로고
    • Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient
    • Peden AH, Head MW, Ritchie DL, Bell JE, Ironside JW. Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient. Lancet 2004;364:527-9.
    • (2004) Lancet , vol.364 , pp. 527-529
    • Peden, A.H.1    Head, M.W.2    Ritchie, D.L.3    Bell, J.E.4    Ironside, J.W.5
  • 17
  • 18
    • 33745440706 scopus 로고    scopus 로고
    • Kuru in the 21st century-an acquired human prion disease with very long incubation periods
    • Collinge J, Whitfield J, McKintosh E, Beck J, Mead S, Thomas DJ, et al. Kuru in the 21st century-an acquired human prion disease with very long incubation periods. Lancet 2006;367:2068-74.
    • (2006) Lancet , vol.367 , pp. 2068-2074
    • Collinge, J.1    Whitfield, J.2    McKintosh, E.3    Beck, J.4    Mead, S.5    Thomas, D.J.6
  • 19
    • 33646059507 scopus 로고    scopus 로고
    • Predicting susceptibility and incubation time of human-to-human transmission of vCJD
    • Bishop MY, Hart P, Aitchison L. Predicting susceptibility and incubation time of human-to-human transmission of vCJD. Lancet Neurol 2006;5:393-8.
    • (2006) Lancet Neurol , vol.5 , pp. 393-398
    • Bishop, M.Y.1    Hart, P.2    Aitchison, L.3
  • 20
    • 33646354953 scopus 로고    scopus 로고
    • Of mice and men... and vCJD
    • Lasmézas CI. Of mice and men... and vCJD. Lancet Neurol 2006;5:374-5.
    • (2006) Lancet Neurol , vol.5 , pp. 374-375
    • Lasmézas, C.I.1
  • 21
    • 33646898809 scopus 로고    scopus 로고
    • Variant Creutzfeldt-Jakob disease: Prion protein genotype analisis and positive appendix tissue samples from a retrospective prevalence study
    • Ironside JW, Bishop MT, Connoly K. Variant Creutzfeldt-Jakob disease: prion protein genotype analisis and positive appendix tissue samples from a retrospective prevalence study. BMJ 2006;332:1166-8.
    • (2006) BMJ , vol.332 , pp. 1166-1168
    • Ironside, J.W.1    Bishop, M.T.2    Connoly, K.3
  • 22
    • 33745879463 scopus 로고    scopus 로고
    • Presymptomatic detection of prions in blood
    • Saa P, Casilla J, Soto C. Presymptomatic detection of prions in blood. Science 2006;313:92-4.
    • (2006) Science , vol.313 , pp. 92-94
    • Saa, P.1    Casilla, J.2    Soto, C.3
  • 23
    • 33749236787 scopus 로고    scopus 로고
    • A systematic review of prion therapeutics in experimental models
    • Trevitt C, Collinge J. A systematic review of prion therapeutics in experimental models. Brain 2006;129:2241-65.
    • (2006) Brain , vol.129 , pp. 2241-2265
    • Trevitt, C.1    Collinge, J.2
  • 25
    • 0031914675 scopus 로고    scopus 로고
    • Detection of 14-3-3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt-Jakob disease
    • Zerr I, Bodemer M, Gefelleer O, Otto M, Poser S, Wiltfang J, et al. Detection of 14-3-3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt-Jakob disease. Ann Neurol 1998;43:32-40.
    • (1998) Ann Neurol , vol.43 , pp. 32-40
    • Zerr, I.1    Bodemer, M.2    Gefelleer, O.3    Otto, M.4    Poser, S.5    Wiltfang, J.6
  • 29
    • 8944259890 scopus 로고    scopus 로고
    • Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease
    • Parchi P, Castellani R, Capellari S, Ghetti B, Young K, Chen SG, et al. Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease. Ann Neurol 1996;39:669-80.
    • (1996) Ann Neurol , vol.39 , pp. 669-680
    • Parchi, P.1    Castellani, R.2    Capellari, S.3    Ghetti, B.4    Young, K.5    Chen, S.G.6
  • 30
    • 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, Schultz-Schaeffer W, Windl O, et al. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects. Ann Neurol 1999;46: 224-33.
    • (1999) Ann Neurol , vol.46 , pp. 224-233
    • Parchi, P.1    Giese, A.2    Capellari, S.3    Brown, P.4    Schultz-Schaeffer, W.5    Windl, O.6
  • 33
    • 2542618458 scopus 로고    scopus 로고
    • Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: UK cases 1991-2002
    • Head MW, Bunn T, Bishop MT, McLouglin V, Lowrie S, McKimmie CS, et al. Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: UK cases 1991-2002. Ann Neurol 2004;55:851-9.
    • (2004) Ann Neurol , vol.55 , pp. 851-859
    • Head, M.W.1    Bunn, T.2    Bishop, M.T.3    McLouglin, V.4    Lowrie, S.5    McKimmie, C.S.6
  • 34
    • 33745897112 scopus 로고    scopus 로고
    • Long-duration sCJD with PRNP codon 129 methionine homozygosity and cerebral cortical plaques
    • Lo RY-Y, Shyu WC, Li, H. Long-duration sCJD with PRNP codon 129 methionine homozygosity and cerebral cortical plaques. Neurology 2006;66:1944-5.
    • (2006) Neurology , vol.66 , pp. 1944-1945
    • Lo, R.Y.-Y.1    Shyu, W.C.2    Li, H.3
  • 35
    • 0032763817 scopus 로고    scopus 로고
    • Sporadic Creutzfeldt-Jakob disease: Co-occurrence of different types of PrPsc in the same brain
    • Puoti G, Giaccone G, Rossi G, Canciani B, Bugiani O, Tagliavini F. Sporadic Creutzfeldt-Jakob disease: co-occurrence of different types of PrPsc in the same brain. Neurology 1999;53:2173-6.
    • (1999) Neurology , vol.53 , pp. 2173-2176
    • Puoti, G.1    Giaccone, G.2    Rossi, G.3    Canciani, B.4    Bugiani, O.5    Tagliavini, F.6
  • 40
    • 0032778175 scopus 로고    scopus 로고
    • Multiple prion type in the same brain. Is a molecular diagnosis de CJD posible?
    • Dickson DW, Brown P. Multiple prion type in the same brain. Is a molecular diagnosis de CJD posible? Neurology 1999;53:1903-4.
    • (1999) Neurology , vol.53 , pp. 1903-1904
    • Dickson, D.W.1    Brown, P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.