A new variant of Creutzfeldt-Jakob disease: Neuropathological and clinical features

Cold Spring Harbor Symposia on Quantitative Biology

Volumn 61, Issue , 1996, Pages 523-530

  Ironside, J W ^a   Sutherland, K ^a   Bell, J E ^a   Mccardle, L ^a   Barrie, C ^a   Estebeiro, K ^a   Zeidler, M ^a   Will, R G ^a  

^a WESTERN GENERAL HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CONFERENCE PAPER; CREUTZFELDT JAKOB DISEASE; HUMAN; PRION; PRIORITY JOURNAL; UNITED KINGDOM; VIRUS GENE; VIRUS TRANSMISSION; ADOLESCENT; ADULT; ARTICLE; ASTROCYTOSIS; CLINICAL ARTICLE; CLINICAL FEATURE; CODON; DISEASE DURATION; DISEASE SURVEILLANCE; DYSESTHESIA; ELECTROENCEPHALOGRAM; FEMALE; GENOTYPE; IMAGE ANALYSIS; IMMUNOCYTOCHEMISTRY; MALE; MENTAL DISEASE; NEUROPATHOLOGY; ONSET AGE;

EID: 0030427254     PISSN: 00917451     EISSN: None     Source Type: Book Series    
DOI: 10.1101/sqb.1996.061.01.052     Document Type: Conference Paper

References (31)

1. Anon. 1987. Scrapie-like disease in a captive nyala. In Animal health. Report of the Chief Veterinary Officer, p.69. HMSO, London.
2. Bateman, D., D. Hilton, S. Love, M. Zeidler, J. Beck, and J. Collinge. 1995. Sporadic Creutzfeldt-Jakob disease in a 18-year old in the UK. Lancet 346: 1155.
3. Bell, J.E. and J.W. Ironside. 1993. Neuropathology of spongiform encephatopathies in humans. Br. Med. Bull. 49: 738.
4. Berman, P., G.S. Davidson, and L.E. Becker. 1988. Progressive neurological deterioration in a 14-year-old girl. Pediatr. Neurosci. 14: 42.
5. Billette de Villemeur, T., A. Gellott, J.P. Deslys, D. Dormont, C. Duyckaerts, L. Jardin, J. Denni, and O. Robain. 1994. Iatrogenic Creutzfeldt-Jakob disease in three growth hormone recipients: A neuropathological study. Neuropathol. Appl. Neurobiol. 20: 111.
6. Britton, T.C., S. Al-Sarraj, C. Shaw, T. Campbell, and J. Collinge. 1995. Sporadic Creutzfeldt-Jakob disease in a 16-year old in the UK. Lancet 346: 1155.
7. Brown, P., M.A. Preece, and R.G. Will. 1992 Friendly fire in medicine: Hormones, homografts, and Creutzfeldt-Jakob disease. Lancet 340: 24.
8. Brown, P., F. Cathala, R.F. Roberts, D.C. Gajdusek, and P. Cataigne. 1987. The epidemiology of Creutzfeldt-Jakob disease: Conclusion of a 15-year investigation in France and review of the world literature. Neurology 37: 895.
9. Brown, P., F. Cathala, R. Labauge, M. Pages, J.C. Alary, and H. Baron. 1985. Epidemiologic implications of Creutzfeidt-Jakob disease in a 19-year old girl. Eur. J. Epidemiol. 1: 42.
10. Bruce, M.E., I. McConnell, H. Fraser, and A.G. Dickinson. 1991. The disease characteristics of different strains of scrapie in Sinc congenic mouse lines: Implications for the nature of the agent and host controls of pathogenesis. J. Gen. Virol. 72: 595.
11. Bruton, C.J., R.K. Bruton, S.M. Gentleman, and G.W. Roberts. 1995. Diagnosis and incidence of prion (Creutzfeldt-Jakob) disease: A retrospective archival study with implications for future research. Neurodegeneration 4: 357.
12. Budka, H., A. Aguzzi, P. Brown, J.-M. Brucher, O. Bugiani, F. Gullotta, M. Haltia, J.-J. Hauw, J.W. Ironside, K. Jellinger, H.A. Kretzschmar, P.L. Lantos, C. Masullo, W. Schlote, J. Tateishi, and R.O. Weller. 1995. Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (priori diseases). Brain Pathol. 5: 459.
13. Chazot, G., E. Broussolle, CL. Lapras, T. Blattler, A. Aguzzi, and N. Kopp. 1996. New variant of Creuizfeidt-Jakob disease in a 26-year-old French man. Lancet 347: 1181.
14. Collinge, J., M.S. Palmer, and A.J. Dryden. 1991. Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease. Lancet 337: 1441.
15. Cousens, S.N., R. Harries-Jones, R. Knight, R. Will, P.G. Smith, and W.B. Matthews. 1990. Geographical distribution of cases of Creutzfeldt-Jakob disease in England and Wales 1970-84. J. Neurol. Neurosurg. Psychiatry 53: 459.
16. de Silva, R., J.W. Ironside, L. McCardle, T.F.G. Esmonde, J.E. Bell, and R.G. Will. 1994. Neuropathological phenotype and "prion protein" genotype correlation in sporadic Creutzfeldt-Jakob disease. Neurosci. Lett. 179: 50.
17. Delasnerie-Laupretre, N., S. Poser, M. Pocchiari, D.P.W.M. Wientjens, and R.G. Will. 1995. Incidence of Creutzfeldt-Jakob disease in Europe. Lancet 346: 898.
18. Goodbrand, I.A., J.W. Ironside, D. Nicolson, and J. E. Bell. 1995. Prion protein accumulation in the spinal cords of patients with sporadic and growth hormone associated Creutzfeldt-Jakob disease. Neurosci. Lett. 183: 27.
19. Klatzo, I., D.C. Gajdusek, and V. Zigas. 1959. Pathology of kuru. Lab. Invest. 8: 799.
20. Kulczycki, J., H. Jedrzejowska, K. Gajkowski, E. Tamowska-Dzidusko, and W. Lojkowska. 1991. Creutzfeldt-Jakob disease in young people. Eur. J. Epidemiol. 7: 501.
21. Lasmezas, C.I., J.-P. Deslys, R. Demaimay, K.T. Adjou, F. Lamoury, D. Dormont, O. Roubain, J. Ironside, and J.-J. Hauw. 1996. BSE transmission to macaques. Nature 381: 743.
22. MacDonald, S.T., K. Sutherland, and J.W. Ironside. 1996. Prion protein genotype and pathological phenotype studies in sporadic Creutzfeldt-Jakob disease. Neuropathol. Appl. Neurobiol. 22: 285.
23. Medori, R., H.J. Trischler, A. LeBlanc, F. Villare, V. Manetto, H.Y. Chen, R. Xue, S. Leal, P. Montagna, P. Cortelli, P. Tinuper, P. Avoni, M. Mochi, A. Baruzzi, J.J. Hauw, J. Ott, E. Lugaresi, L. Autilio-Gambetti, and P. Gambetti. 1992. Fatal familial insomnia is a prion disease with a mutation at codon 178 of the prion gene. N. Eng. J. Med. 326: 444.
24. Monreal, J., G.H. Collings, C.L. Masters, C. M. Fisher, C. Kim C.J. Gibbs Jr., and D.C. Gajdusek. 1981. Creutzfeldt-Jakob disease in an adolescent. J. Neurol. Sci. 52: 341.
25. Packer, R.J., D.R. Comblath, N.K. Gonatas, L.A. Bruno, and A.K. Asbury. 1980. Creutzfeldt-Jakob disease in a 20-year old woman. Neurology 30: 492.
26. Palmer, M.S., A.J. Dryden, J.T. Hughes, and J. Collinge. 1991. Homozygous prion protein genotype predisposes to sporadic Creutzfeldt-Jakob disease. Nature 352: 340.
27. Prusiner, S.B. 1993. Genetic and infectious prion diseases. Arch. Neurol. 50: 1129.
28. Sutherland, K., S.T. Macdonald, and J.W. Ironside. 1996. Quantification and analysis of the neuropathological features of Creutzfeldt-Jakob disease. J. Neurosci. Methods 64: 123.
29. The National CJD Surveillance Unit, and the Department of Epidemiology and Population Sciences, London School of Hygiene and Tropical Medicine. 1995. Creutzfeldt-Jakob disease surveillance in the United Kingdom: 4th Annual Report.
30. Wells, G.A.H., A.C. Scott, C.T. Johnson, R.F. Gunning, R.D. Hancock, M. Jeffrey, M. Dawson, and R. Bradley. 1987. A novel progressive spongiform encephalopatby in cattle. Vet. Rec. 121: 419.
31. Will, R.G., J.W. Ironside, M. Zeidler, S.N. Cousens, K. Estebeiro, A. Alperovitch, S. Poser, M. Poochiari, A. Hofman, and P.C. Smith. 1996. A new variant of Creutzfeldt-Jakob disease in the UK. Lancet 347: 921.