Aspekty kliniczne chorób prionowych

作者: Richard Knight

DOI:

关键词: Iatrogenic Creutzfeldt-Jakob diseaseMedicineDermatologyVariant Creutzfeldt–Jakob disease

摘要:

参考文章(40)
Ana B Rodríguez-Martínez, Joseba M Garrido, Juan J Zarranz, Jose M Arteagoitia, Marian M de Pancorbo, Begoña Atarés, Miren J Bilbao, Isidro Ferrer, Ramón A Juste, A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case report BMC Neurology. ,vol. 10, pp. 99- 99 ,(2010) , 10.1186/1471-2377-10-99
P. Brown, J.-P. Brandel, M. Preese, T. Sato, Iatrogenic Creutzfeldt–Jakob disease: The waning of an era Neurology. ,vol. 67, pp. 389- 393 ,(2006) , 10.1212/01.WNL.0000231528.65069.3F
D.A. Collie, R.J. Sellar, M. Zeidler, A.C.F. Colchester, R. Knight, R.G. Will, MRI of Creutzfeldt-Jakob disease: imaging features and recommended MRI protocol. Clinical Radiology. ,vol. 56, pp. 726- 739 ,(2001) , 10.1053/CRAD.2001.0771
M. H. Nurmi, M. Bishop, L. Strain, F. Brett, C. McGuigan, M. Hutchison, M. Farrell, R. Tilvis, S. Erkkilä, O. Simell, R. Knight, M. Haltia, The normal population distribution of PRNP codon 129 polymorphism. Acta Neurologica Scandinavica. ,vol. 108, pp. 374- 378 ,(2003) , 10.1034/J.1600-0404.2003.00199.X
Ignazio Cali, Rudolph Castellani, Amer Alshekhlee, Yvonne Cohen, Janis Blevins, Jue Yuan, Jan P. M. Langeveld, Piero Parchi, Jiri G. Safar, Wen-Quan Zou, Pierluigi Gambetti, Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics. Brain. ,vol. 132, pp. 2643- 2658 ,(2009) , 10.1093/BRAIN/AWP196
Mark W. Head, Suzanne Lowrie, Gurjit Chohan, Richard Knight, David J. Scoones, James W. Ironside, Variably protease-sensitive prionopathy in a PRNP codon 129 heterozygous UK patient with co-existing tau, α synuclein and Aβ pathology Acta Neuropathologica. ,vol. 120, pp. 821- 823 ,(2010) , 10.1007/S00401-010-0766-Y
M.-A. Macleod, G. E. Stewart, M. Zeidler, R. Will, R. Knight, Sensory features of variant Creutzfeldt-Jakob disease. Journal of Neurology. ,vol. 249, pp. 706- 711 ,(2002) , 10.1007/S00415-002-0696-2