Skip to main content
Journal of Clinical Pathology logoLink to Journal of Clinical Pathology
. 1998 Apr;51(4):265–269. doi: 10.1136/jcp.51.4.265

Prion diseases: what will be next?

P van der Valk 1
PMCID: PMC500667  PMID: 9659236

Full text

PDF
265

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Aguzzi A. Between cows and monkeys. Nature. 1996 Jun 27;381(6585):734–734. doi: 10.1038/381734a0. [DOI] [PubMed] [Google Scholar]
  2. Aguzzi A. Neuro-immune connection in spread of prions in the body? Lancet. 1997 Mar 15;349(9054):742–743. doi: 10.1016/S0140-6736(97)22011-8. [DOI] [PubMed] [Google Scholar]
  3. Alper T., Cramp W. A., Haig D. A., Clarke M. C. Does the agent of scrapie replicate without nucleic acid? Nature. 1967 May 20;214(5090):764–766. doi: 10.1038/214764a0. [DOI] [PubMed] [Google Scholar]
  4. Berger J. R., David N. J. Creutzfeldt-Jakob disease in a physician: a review of the disorder in health care workers. Neurology. 1993 Jan;43(1):205–206. doi: 10.1212/wnl.43.1_part_1.205. [DOI] [PubMed] [Google Scholar]
  5. Brown P., Gajdusek D. C. The human spongiform encephalopathies: kuru, Creutzfeldt-Jakob disease, and the Gerstmann-Sträussler-Scheinker syndrome. Curr Top Microbiol Immunol. 1991;172:1–20. doi: 10.1007/978-3-642-76540-7_1. [DOI] [PubMed] [Google Scholar]
  6. Brown P., Gibbs C. J., Jr, Rodgers-Johnson P., Asher D. M., Sulima M. P., Bacote A., Goldfarb L. G., Gajdusek D. C. Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease. Ann Neurol. 1994 May;35(5):513–529. doi: 10.1002/ana.410350504. [DOI] [PubMed] [Google Scholar]
  7. Brown P., Preece M. A., Will R. G. "Friendly fire" in medicine: hormones, homografts, and Creutzfeldt-Jakob disease. Lancet. 1992 Jul 4;340(8810):24–27. doi: 10.1016/0140-6736(92)92431-e. [DOI] [PubMed] [Google Scholar]
  8. Budka H., Aguzzi A., Brown P., Brucher J. M., Bugiani O., Collinge J., Diringer H., Gullotta F., Haltia M., Hauw J. J. Tissue handling in suspected Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases) Brain Pathol. 1995 Jul;5(3):319–322. doi: 10.1111/j.1750-3639.1995.tb00609.x. [DOI] [PubMed] [Google Scholar]
  9. Büeler H., Aguzzi A., Sailer A., Greiner R. A., Autenried P., Aguet M., Weissmann C. Mice devoid of PrP are resistant to scrapie. Cell. 1993 Jul 2;73(7):1339–1347. doi: 10.1016/0092-8674(93)90360-3. [DOI] [PubMed] [Google Scholar]
  10. Collinge J., Sidle K. C., Meads J., Ironside J., Hill A. F. Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD. Nature. 1996 Oct 24;383(6602):685–690. doi: 10.1038/383685a0. [DOI] [PubMed] [Google Scholar]
  11. DeArmond S. J., Prusiner S. B. Prion protein transgenes and the neuropathology in prion diseases. Brain Pathol. 1995 Jan;5(1):77–89. doi: 10.1111/j.1750-3639.1995.tb00579.x. [DOI] [PubMed] [Google Scholar]
  12. Drobniewski F. Is death inevitable with multiresistant TB plus HIV infection? Lancet. 1997 Jan 11;349(9045):71–72. doi: 10.1016/S0140-6736(05)60878-1. [DOI] [PubMed] [Google Scholar]
  13. GAJDUSEK D. C., ZIGAS V. Kuru; clinical, pathological and epidemiological study of an acute progressive degenerative disease of the central nervous system among natives of the Eastern Highlands of New Guinea. Am J Med. 1959 Mar;26(3):442–469. doi: 10.1016/0002-9343(59)90251-7. [DOI] [PubMed] [Google Scholar]
  14. Gambetti P., Parchi P., Petersen R. B., Chen S. G., Lugaresi E. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: clinical, pathological and molecular features. Brain Pathol. 1995 Jan;5(1):43–51. doi: 10.1111/j.1750-3639.1995.tb00576.x. [DOI] [PubMed] [Google Scholar]
  15. Gasset M., Baldwin M. A., Fletterick R. J., Prusiner S. B. Perturbation of the secondary structure of the scrapie prion protein under conditions that alter infectivity. Proc Natl Acad Sci U S A. 1993 Jan 1;90(1):1–5. doi: 10.1073/pnas.90.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Ghetti B., Dlouhy S. R., Giaccone G., Bugiani O., Frangione B., Farlow M. R., Tagliavini F. Gerstmann-Sträussler-Scheinker disease and the Indiana kindred. Brain Pathol. 1995 Jan;5(1):61–75. doi: 10.1111/j.1750-3639.1995.tb00578.x. [DOI] [PubMed] [Google Scholar]
  17. Goldfarb L. G., Petersen R. B., Tabaton M., Brown P., LeBlanc A. C., Montagna P., Cortelli P., Julien J., Vital C., Pendelbury W. W. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism. Science. 1992 Oct 30;258(5083):806–808. doi: 10.1126/science.1439789. [DOI] [PubMed] [Google Scholar]
  18. Hill A. F., Zeidler M., Ironside J., Collinge J. Diagnosis of new variant Creutzfeldt-Jakob disease by tonsil biopsy. Lancet. 1997 Jan 11;349(9045):99–100. doi: 10.1016/S0140-6736(97)24002-X. [DOI] [PubMed] [Google Scholar]
  19. Lasmézas C. I., Deslys J. P., Demaimay R., Adjou K. T., Lamoury F., Dormont D., Robain O., Ironside J., Hauw J. J. BSE transmission to macaques. Nature. 1996 Jun 27;381(6585):743–744. doi: 10.1038/381743a0. [DOI] [PubMed] [Google Scholar]
  20. Manuelidis L., Fritch W., Xi Y. G. Evolution of a strain of CJD that induces BSE-like plaques. Science. 1997 Jul 4;277(5322):94–98. doi: 10.1126/science.277.5322.94. [DOI] [PubMed] [Google Scholar]
  21. McKinley M. P., Bolton D. C., Prusiner S. B. A protease-resistant protein is a structural component of the scrapie prion. Cell. 1983 Nov;35(1):57–62. doi: 10.1016/0092-8674(83)90207-6. [DOI] [PubMed] [Google Scholar]
  22. Muramoto T., Kitamoto T., Tateishi J., Goto I. The sequential development of abnormal prion protein accumulation in mice with Creutzfeldt-Jakob disease. Am J Pathol. 1992 Jun;140(6):1411–1420. [PMC free article] [PubMed] [Google Scholar]
  23. Oesch B., Westaway D., Wälchli M., McKinley M. P., Kent S. B., Aebersold R., Barry R. A., Tempst P., Teplow D. B., Hood L. E. A cellular gene encodes scrapie PrP 27-30 protein. Cell. 1985 Apr;40(4):735–746. doi: 10.1016/0092-8674(85)90333-2. [DOI] [PubMed] [Google Scholar]
  24. Owen F., Poulter M., Collinge J., Crow T. J. Codon 129 changes in the prion protein gene in Caucasians. Am J Hum Genet. 1990 Jun;46(6):1215–1216. [PMC free article] [PubMed] [Google Scholar]
  25. Prusiner S. B., DeArmond S. J. Molecular biology and pathology of scrapie and the prion diseases of humans. Brain Pathol. 1991 Jul;1(4):297–310. doi: 10.1111/j.1750-3639.1991.tb00673.x. [DOI] [PubMed] [Google Scholar]
  26. Prusiner S. B., Groth D. F., Bolton D. C., Kent S. B., Hood L. E. Purification and structural studies of a major scrapie prion protein. Cell. 1984 Aug;38(1):127–134. doi: 10.1016/0092-8674(84)90533-6. [DOI] [PubMed] [Google Scholar]
  27. Prusiner S. B. Novel proteinaceous infectious particles cause scrapie. Science. 1982 Apr 9;216(4542):136–144. doi: 10.1126/science.6801762. [DOI] [PubMed] [Google Scholar]
  28. Richardson E. P., Jr, Masters C. L. The nosology of Creutzfeldt-Jakob disease and conditions related to the accumulation of PrPCJD in the nervous system. Brain Pathol. 1995 Jan;5(1):33–41. doi: 10.1111/j.1750-3639.1995.tb00575.x. [DOI] [PubMed] [Google Scholar]
  29. Ridley R. M., Baker H. F., Windle C. P. Failure to transmit bovine spongiform encephalopathy to marmosets with ruminant-derived meal. Lancet. 1996 Jul 6;348(9019):56–56. doi: 10.1016/s0140-6736(05)64377-2. [DOI] [PubMed] [Google Scholar]
  30. Telling G. C., Scott M., Hsiao K. K., Foster D., Yang S. L., Torchia M., Sidle K. C., Collinge J., DeArmond S. J., Prusiner S. B. Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein. Proc Natl Acad Sci U S A. 1994 Oct 11;91(21):9936–9940. doi: 10.1073/pnas.91.21.9936. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Wells G. A., McGill I. S. Recently described scrapie-like encephalopathies of animals: case definitions. Res Vet Sci. 1992 Jul;53(1):1–10. doi: 10.1016/0034-5288(92)90076-e. [DOI] [PubMed] [Google Scholar]
  32. Wells G. A., Scott A. C., Johnson C. T., Gunning R. F., Hancock R. D., Jeffrey M., Dawson M., Bradley R. A novel progressive spongiform encephalopathy in cattle. Vet Rec. 1987 Oct 31;121(18):419–420. doi: 10.1136/vr.121.18.419. [DOI] [PubMed] [Google Scholar]
  33. Wells G. A., Wilesmith J. W. The neuropathology and epidemiology of bovine spongiform encephalopathy. Brain Pathol. 1995 Jan;5(1):91–103. doi: 10.1111/j.1750-3639.1995.tb00580.x. [DOI] [PubMed] [Google Scholar]
  34. Wilesmith J. W., Wells G. A., Cranwell M. P., Ryan J. B. Bovine spongiform encephalopathy: epidemiological studies. Vet Rec. 1988 Dec 17;123(25):638–644. [PubMed] [Google Scholar]
  35. Will R. G., Ironside J. W., Zeidler M., Cousens S. N., Estibeiro K., Alperovitch A., Poser S., Pocchiari M., Hofman A., Smith P. G. A new variant of Creutzfeldt-Jakob disease in the UK. Lancet. 1996 Apr 6;347(9006):921–925. doi: 10.1016/s0140-6736(96)91412-9. [DOI] [PubMed] [Google Scholar]
  36. Will R. G., Matthews W. B. Evidence for case-to-case transmission of Creutzfeldt-Jakob disease. J Neurol Neurosurg Psychiatry. 1982 Mar;45(3):235–238. doi: 10.1136/jnnp.45.3.235. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. van Keulen L. J., Schreuder B. E., Meloen R. H., Mooij-Harkes G., Vromans M. E., Langeveld J. P. Immunohistochemical detection of prion protein in lymphoid tissues of sheep with natural scrapie. J Clin Microbiol. 1996 May;34(5):1228–1231. doi: 10.1128/jcm.34.5.1228-1231.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Clinical Pathology are provided here courtesy of BMJ Publishing Group

RESOURCES