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人类朊毒体病的研究进展 被引量:1

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出处 《中国实用内科杂志》 CAS CSCD 北大核心 2005年第9期854-856,共3页 Chinese Journal of Practical Internal Medicine
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参考文献10

  • 1Aguzzi A,Polymenidou M.Mammalian prion biology: one century of evolving concepts.Cell,2004,116:313-327.
  • 2李梦东,聂青和.朊毒体的研究进展[J].中华传染病杂志,1999,17(1):62-64. 被引量:3
  • 3Collins SJ,Lawson VA,Masters PC.Transmissible spongiform encephalopathies.Lancet,2004,363:51-61.
  • 4Unterberger U,Voigtlander T,Budka H.Pathogenesis of prion diseases.Acta Neuropathologica,2005,109:32-48.
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  • 6Collinge J.Molecular neurology of prion disease.J Neurol Neurosurg Psychiatry,2005,76:906-925.
  • 7Gerard L,Géraldine M.The population distribution of the Met allele at the PRNP129 polymorphism (a high risk factor for Creutzfeldt-Jakob disease) in various regions of France and in West Europe.Infect Genet Evol,2005,5:141-144.
  • 8Notari S,Capellari S,Giese A,et al.Effects of different experimental conditions on the PrPSc core generated by protease digestion: implications for strain typing and molecular classification of CJD.J Biol Chem,2004,279:16797-16804.
  • 9Tanaka M,Chien P,Naber N,et al.Conformational variations in an infectious protein determine prion strain differences.Nature,2004,428:323-328.
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二级参考文献27

  • 1Brown DR, Wong BS, Hafiz F, et al. Normal prion protein has an activity like that of superoxide dismutase[J]. Biochem, 1999, 344: 1-5.
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共引文献8

同被引文献14

  • 1杨银升,杨金升,石向群,王娟,陈合成.克-雅病患者间断脑电图监测8例报告[J].临床神经电生理学杂志,2007,16(1):37-40. 被引量:5
  • 2聂青和.人类朊毒体病的诊治及预防[J].临床内科杂志,2005,22(8):508-511. 被引量:3
  • 3聂青和.朊毒体及人类朊毒体病//李梦东,王宇明.实用传染病学[M].3版.北京:人民卫生出版社,2004:614-630.
  • 4Prusiner SB. Prion diseases and the BSE crisis [J]. Science, 1997,278(5336) :245-251.
  • 5Wood H. Prion disease: New techniques developed for prion detection in blood and cerebrospinal fluid [J]. Nat Rev Neurol, 2011,7(4) :183.
  • 6聂青和,李梦东.Prion感染(朊毒体病)//王宇明,顾长海.感染病学新进展[M].北京:人民卫生出版社,2001:308-323.
  • 7Safar JG, Geschwind MD, Deering C, et al. Diagnosis of human prion disease [J]. Proc Natl Acad Sci U S A, 2005,102 (9) :3501- 3506.
  • 8Schlenska GK, Walter GF. Temporal evolution of electroencephalographic abnormalities in Creutzfeldt-Jakob disease [J]. J Neurol, 1989,236(8) :456-460.
  • 9Puoti G, Bizzi A, Forloni G, et al. Sporadic human prion diseases: molecular insights and diagnosis [J]. Lancet Neurol, 2012, 11(7):618-628.
  • 10Gadgil NM, Chaudhari CS, Gohil SD, et al. Creutzfeldt Jacob disease: an autopsy case report in tertiary care hospital [J]. Indian J Pathol Microbiol, 2012,55(1):97-99.

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