1. Some new aspects of CJD epidemiology in Slovakia

   • E. Mitrova

   OriginalPaper Pages: 439 - 449

2. “Clusters” of CJD in Slovakia: The first statistically significant temporo-spatial accumulations of rural cases

   • E. Mitrová
   • M. Bronis

   OriginalPaper Pages: 450 - 456

3. Creutzfeldt-Jakob disease in the last 5 years in Hungary

   • K. Maytenyi

   OriginalPaper Pages: 457 - 459

4. Epidemiological surveillance of Creutzfeldt-Jakob disease in the United Kingdom

   • R. G. Will

   OriginalPaper Pages: 460 - 465

5. Risk of Creutzfeldt-Jakob disease in relation to animal spongiform encephalopathies: A collaborative study in Europe

   • A. Hofman

   OriginalPaper Pages: 466 - 468

6. The phenotypic expression of different mutations in transmissible familial Creutzfeldt-Jakob disease

   • P. Brown
   • L. G. Goldfarb
   • D. C. Gajdusek

   OriginalPaper Pages: 469 - 476

7. Creutzfeldt-Jacob disease associated with the PRNP codon 200^LYS mutation: An analysis of 45 families

   • L. G. Goldfarb
   • P. Brown
   • D. C. Gajdusek

   OriginalPaper Pages: 477 - 486

8. Focal accumulation of CJD in Slovakia: Retrospective investigation of a new rural familial cluster

   • E. Mitrová
   • P. Brown
   • J. Žilâk

   OriginalPaper Pages: 487 - 489

9. Creutzfeldt-Jakob disease among libyan jews

   • A. D. Korczyn

   OriginalPaper Pages: 490 - 493

10. Familial Creutzfeldt-Jakob disease in Finland: Epidemiological, clinical, pathological and molecular genetic studies

    • M. Haltia
    • J. Kovanen
    • D. C. Gajdusek

    OriginalPaper Pages: 494 - 500

11. Creutzfeldt-Jakob disease in young people

    • J. Kulczycki
    • H. Jedrzejowska
    • W. Lojkowska

    OriginalPaper Pages: 501 - 504

12. PrP amyloid plaques in Creutzfeldt-Jakob disease of short duration: immunohistochemical studies of 5 cases from Poland.

    • P. P. Liberski
    • H. Kwiecinski
    • D. C. Gajdusek

    OriginalPaper Pages: 505 - 510

13. Creutzfeldt-Jakob disease — clinical picture analysis

    • M. Drobny
    • V. Krajnak
    • B. Pithova

    OriginalPaper Pages: 511 - 516

14. Clinical, laboratory, and morphological diagnosis of human subacute spongiform encephalopathies in byelorussia

    • I. I. Protas
    • N. D. Kolomietz
    • E. K. Milkamanovich

    BriefCommunication Pages: 517 - 519

15. “Clusters” of CJD in Slovakia: The first laboratory evidence of scrapie

    • E. Mitrová
    • S. Hunčaga
    • M. Tatara

    OriginalPaper Pages: 520 - 523

16. Slow neurological diseases (scrapie and visna) of the sheep in the USSR

    • V. A. Shubin
    • B. F. Shuljak
    • V. C. Kuvshinov

    BriefCommunication Pages: 524 - 525

17. Some problems of diagnosis of the spongiform encephalopathies in ruminants

    • S. Ghergariu

    OriginalPaper Pages: 526 - 531

18. Bovine spongiform encephalopathy (BSE): The current situation and research

    • R. Bradley

    OriginalPaper Pages: 532 - 544

19. Mechanism of the damage to myelinated axons in experimental Creutzfeldt-Jakob disease in mice: An ultrastructural study

    • P. P. Liberski
    • R. Yanagihara
    • D. C. Gajdusek

    OriginalPaper Pages: 545 - 550

20. Tubulovesicular structures in human and experimental Creutzfeldt-Jakob disease

    • P. P. Liberski
    • H. Budka
    • H. Kwiecinski

    OriginalPaper Pages: 551 - 555

21. Experimental drug treatment of scrapie: A pathogenetic basis for rationale therapeutics

    • M. Pocchiari
    • M. Salvatore
    • C. Masullo

    OriginalPaper Pages: 556 - 561

22. Transmissible spongiform encephalopathies (TSE) virus-induced amyloidoses of the central nervous system (CNS)

    • H. Diringer

    OriginalPaper Pages: 562 - 566

23. The transmissible amyloidoses: Genetical control of spontaneous generation of infectious amyloid proteins by nucleation of configurational change in host precursors: Kuru-CJD-GSS-Scrapie-BSE

    • D. C. Gajdusek

    OriginalPaper Pages: 567 - 577

24. Books

    Legacy Pages: 578 - 578