Læknablaðið

Ukioqatigiit

Læknablaðið - 15.07.2008, Qupperneq 36

Læknablaðið - 15.07.2008, Qupperneq 36
■ FRÆÐIGREINAR Y F I R L I T Heimildir 1. Sánchez-Juan PJ. Etiologic and diagnostic facets ofCreutzfeldt- Jakob disease. The effect of genes and environment. Chapter 2.1 The "NEUROCJD" collaboration: CJD surveillance systems and results in 10 countries. (dissertation). Rotterdam, 2007. 2. Will RG, Alperovitch A, Poser S, et al. Descriptive epidemiology of Creutzfeldt-Jakob disease in six European countries, 1993-1995. Ann Neurol 1998; 43: 763- 7. 3. Ladogana A, Puopolo M, Croes EA, et al. Mortality from Creutzfeldt-Jakob disease and related disorders in Europe, Australia and Canada. Neurol 2005; 64:1586-91. 4. Brown P, Gibbs CJ, Rodgers-Johnson P, et al. Human spongiform encephalopathy: The National Instiutes of Health series of 300 cases of experimentally transmitted disease. Ann Neurol 1994; 35: 513-529. 5. Parchi P, Giese A, Capellari S, et al.Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects. Ann Neurol 1999; 46: 224-33. 6. Prusiner SB. Novel proteinaceous infectious particles cause scrapie. Science 1982; 216:136-44. 7. Oesch B, Westaway D, Wálchli M, et al. A cellular gene encodes scrapie 27-30 protein. Cell 1985; 40: 735-46. 8. Bueler H, Fischer M, Lang Y, et al. Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein. Nature 1992; 356: 577-82. 9. Ma J, Wollmann R, Lindquist S. Neurotoxicity and neuro- degeneration when PrP accumulates in the cytosol. Science 2002; 298:1781-5. 10. Roucou X, Guo Qi, Zhang Y, Goodyer CG, LeBlanc AC. Cytosolic prion protein is not toxic and protects against Bax- mediated cell death in human primary neurons. J Biol Chem 2003; 278: 40877-81. 11. Bragason BT, Pálsdóttir A. Interaction of PrP with NRAGE, a protein involved in neuronal apoptosis. Mol Cell Neurosci 2005; 29: 232-44. 12. Prusiner SB. Prions. Proc Natl Acad Sci USA1998; 95:13363- 83. 13. Weissmann C. The state of the prion. Nature Rev Microbiol 2004;2:861-71. 14. Bíieler HR, Aguzzi A, Sailer A, et al. Mice devoid of PrP are resistant to scrapie. Cell 1993; 73:1339-47. 15. Kirby L, Birkett CR., Rudyk H, Gilbert IH, Hope J. In vitro cell-free conversion of bacterial recombinant PrP to PrPres as a model for conversion. J.Gen.Virol. 2003; 84:1013-1020. 16. Legname G, Baskakov IV, Nguyen H-OB, et al. Synthetic mammalian prions. Science 2004; 305: 673-6. 17. Castilla J, Saá P, Hetz C, Soto C. In vitro generation of infectious scrapie prions. Cell 2005; 121:195-206. 18. Pálsson PA. Rida (Scrapie) in Iceland and its epidemiology. In: Prusiner SB and Hadlow WJ, eds Slow Transmissible Diseases of the Nervous System. Vol 1 Academic Press, New York, 1979: 357-66. 19. Hlíðar S. Riða - Polyencephalitis. í: Hlíðar S. Sauðfé og Sauðfjársjúkdómar. Akureyri, Þorsteinn M. Jónsson, 1937: 92-102. 20. Sigurðarson S. Scrapie eller rida i Island. Norsk Vet Tidskr 2000; 112: 408-13. 21. Kahana E, Alter M, Braham J, Sofer D. Creutzfeldt-Jakob disease: Focus among Libyan Jews in Israel. Science 1974; 183: 90-1. 22. Herzberg L, Herzberg BN, Gibbs Jr. CJ, Sullivan W, Amyx H, Gajdusek DC. Creutzfeldt-Jakob disease: Hypothesis for high incidence in Libyan Jews in Israel. Science 1974; 186: 848. 23. Alter M. Athugasemd við grein 22. Science 1974; 186: 848. 24. Collins S, Boyd A, Fletcher A, et al.Creutzfeldt-Jakob disease: diagnostic utility of 14-3-3 protein immunodetection in cerebrospinal fluid. J Clin Neurosci 2000; 7: 203-8. 25. Kovács GG, Gelpi E, Ströbel T, et al. Involvement of the endosomal-lysosomal system correlates with regional pathology in Creutzfeldt-Jakob disease. J Neuropath Exp Neurol 2007; 66: 628-36. 26. O'Rourke KI, Baszler TV, Miller JM, Spraker TR, Sadler- Riggleman I, Knowles DP. Monoclonal antibody F89/160.1.5. defines a conserved epitope on the ruminant prion protein. J Clin Microbiol 1998; 36:1750-5. 27. Georgsson G, Gísladóttir E, Ámadóttir S. Quantitative assessment of the astrocytic response in natural scrapie of sheep. J Comp Path 1993; 108: 229-40. 28. Brownwell B, Oppenheimer DR. An ataxic form of subacute presenile polioencephalopathy (Creutzfeldt-Jakob disease). J Neurol Neurosurg Psychiatry 1965; 28: 350-61. 29. Cooper SA, Murray KL, Heath CA, Will RG, Knight RSG. Sporadic Creutzfeldt- Jakob disease with cerebellar ataxia at onset in the UK. J Neurol Neurosurg Psychiatry 2006; 77: 1273-5. 30. Laplanche J-L, Delasnerie-Laupretre N, Brandel JP, et al. Molecular genetics of prion diseases in France. Neurol 1994; 44: 2347-51. 31. Schulz-Schaeffer WJ, Giese A, Windl O, Kretzschmar HA. Polymorphism at codon 129 of the prion proetein gene determines cerebellar pathology in Creutzfeldt-Jakob disease. Clin Neuropathol 1996; 15: 353-7. 32. Henry C, Lowman A, Will RG. Creutzfeldt- Jakob disease in elderly people. Age Ageing 2002; 31: 7-10. 33. Murray K, Ritchie DL, Bmce M, et al.Sporadic Creutzfeldt- Jakob disease in two adolescents. J Neurol Neurosurg Psychiatry 2008; 79:14-8. 34. Budka H, Aguzzi A, Brown P, et al. Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases). Brain Pathol 1995; 5: 459-66. 35. Georgsson G, Tryggvason T, Jónasdóttir AD, Guðmundsson S, Þorgeirsdóttir S. Polymorphism of PRNP codons in the normal Icelandic population. Acta Neurol Scand 2006; 113: 419-25. 36. Shibuya S, Higuchi J, Shin R-W, Tateishi J, Kitamoto T. Codon 219 lys allele of PRNP is not found in sporadic Creutzfeldt- Jakob disease. Ann Neurol 1998; 43: 826-8. 37. Aguzzi A, Heikenwalder M, Miele G. Progress and problems in the biology, diagnostics, and therapeutics of prion diseases. J Clin Invest 2004; 114:153-160. 38. Jónsson G. Changes in food consumption in Iceland, 1770- 1940. Scand EconomHist Rev 1998; 46: 24-41. 39. Þorgeirsdóttir H. Per Capita Supply of Food in Iceland 1956- 1995. Master thesis (1999) Human Nutrition Department of Food Science, Faculty of Science, University of Iceland. 40. Collinge J, Whitfield J, McKintosh E, et al. Kum in the 21st century-an acquired human prion disease with very long incubation periods. Lancet 2006; 367: 2068-74. 41. Þorgeirsdóttir S, Georgsson G, Reynisson E, Sigurðarson S, Pálsdóttir A.Search for healthy carriers of scrapie: an assessment of subclinical infection of sheep in an Icelandic scrapie flock by three diagnostic methods and correlation with PrP genotypes. Arch Virol 2002; 147: 709-22. 42. Georgsson G, Adolfsdóttir JA, Pálsdóttir A, Jömndsson E, Sigurðarson S, Þorgeirsdóttir S. High incidence of subclinical infection of lymphoid tissues in Scrapie affected sheep flocks. Arch Virol 2008; 153: 637-44. 43. Gísladóttir H. íslensk matarhefð. Mál og menning, Reykjavík 1999. 44. Georgsson G, Sigurðarson S, Brown P. Infectious agent of sheep scrapie may persist in the environment for at least 16 years. J Gen Virol 2006; 87: 3737-40. 45. Mohan J, Brown KL, Farquhar CF, Bmce ME, Mabbott NA. Scrapie transmission following exposure through the skin is dependent on follicular dendritic cells in lymphoid tissues. J Dermatol Sci 2004; 35:101-11. 46. Chatelain J, Cathala F, Brown P, Raharison S, Court L, Gajdusek DC. Epidemiologic comparisons between Creutzfeldt-Jakob disease and scrapie in France during the 12-year period 1968-1979. J Neurol Sci 1981; 51: 329-37. 47. Wientjens DPWM, Davanipour Z, Hofman A, et al. Risk factors for Creutzfeldt-Jakob disease: A reanalysis of case- control studies. Neurol 1996; 46:1287-91. 48. Van Duijn CM, Delasnerie-Laupretre N, Masullo C, et al. Case-control study of risk factors of Creutzfeldt-Jakob Disease in Europe during 1993-95. Lancet; 352:1081-5. 49. Korczyn AD, Chapman J, Goldfarb LG, Brown P, Gajdusek DC. A mutation in the prion protein gene in Creutzfeldt- Jakob disease in Jewish patients of Libyan, Greek, and Tunisian origin. Ann NY Acad Sci 1991; 640:171-6.1) Kvennasviði, 2) myndgreiningarsviði Landspítala. Grein móttekin 25.1.2008, samþykkt til birtingar 19.6.2008 548 LÆKNAblaðiö 2008/94

x

Læknablaðið

Direct Links

Hvis du vil linke til denne avis/magasin, skal du bruge disse links:

Link til denne avis/magasin: Læknablaðið
https://timarit.is/publication/986

Link til dette eksemplar:

Link til denne side:

Link til denne artikel:

Venligst ikke link direkte til billeder eller PDfs på Timarit.is, da sådanne webadresser kan ændres uden advarsel. Brug venligst de angivne webadresser for at linke til sitet.