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Neuropathological Diagnostic-criteria for Creutzfeldt-jakob-disease (cjd) and Other Human Spongiform Encephalopathies (prion Diseases)

Bibliographic reference Budka, H. ; Aguzzi, A. ; Brown, Peter ; Brucher, Jean-Marie ; Bugiani, O. ; et. al. Neuropathological Diagnostic-criteria for Creutzfeldt-jakob-disease (cjd) and Other Human Spongiform Encephalopathies (prion Diseases). In: Brain Pathology, Vol. 5, no. 4, p. 459-466 (1995)
Permanent URL http://hdl.handle.net/2078.1/47641
  1. Bell JE, Brit Med Bull, 49, 738 (1993)
  2. Boellaard J.W., Doerr-Schott J., Schlote W., Miniplaques and shapeless cerebral amyloid deposits in a case of Gerstmann-Str�ussler-Scheinker's syndrome, 10.1007/bf00228593
  3. Brown Paul, Gibbs C. J., Rodgers-Johnson Pamela, Asher David M., Sulima Michael P., Bacote Alfred, Goldfarb Lev G., Gajdusek D. Carleton, Human spongiform encephalopathy: The national institutes of health series of 300 cases of experimentally transmitted disease, 10.1002/ana.410350504
  4. Brown P, Rev Neural (Paris), 148, 317 (1992)
  5. Budka H, Neuropathological diagnostic criteria for brain banking (1995)
  6. Collinge J., Owen F., Poulter M., Leach M., Crow T.J., Rossor M.N., Hardy J., Mullan M.J., Janota I., Lantos P.L., Prion dementia without characteristic pathology, 10.1016/0140-6736(90)91518-f
  7. Will R.G., Diringer H., Bridges LeslieR., Fraser H., Hardy John, Goate Alison, Arya S.C., Prion disease, 10.1016/0140-6736(90)91907-r
  8. Doh-ura K, Ann Neurol, 27, 121 (1990)
  9. Doi-Yi R., Kitamoto T., Ogomori K., Mehraein P., Tateishi J., Distribution of prion protein in German patients with Creutzfeldt-Jakob disease is different from that in Japanese patients, 10.1007/s004010050113
  10. Farlow MR, Handbook of Clinical Neurology, Vol. 16 (60): Hereditary Neuropathies and Spinocerebellar Atrophies, 619 (1991)
  11. Gambetti P, Brain Pathol, 5, 43 (1995)
  12. Ghetti B, Brain Pathol, 5, 61 (1995)
  13. Ghetti B., Tagliavini F., Masters C. L., Beyreuther K., Giaccone G., Verga L., Farlow M. R., Conneally P. M., Dlouhy S. R., Azzarelli B., Bugiani O., Gerstmann-Straussler-Scheinker disease II. Neurofibrillary tangles and plaques with PrP-amyloid coexist in an affected family, 10.1212/wnl.39.11.1453
  14. Goldfarb L., Petersen R., Tabaton M, Brown P, LeBlanc A., Montagna P, Cortelli P, Julien J, Vital C, Pendelbury W., et al., Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism, 10.1126/science.1439789
  15. Gray F., Chr�tien F., Cesaro P., Chatelain J., Beaudry P., Laplanche J. L., Mikol J., Bell J., Gambetti P., Degos J. D., Creutzfeldt-Jakob disease and cerebral amyloid angiopathy, 10.1007/bf00294366
  16. Hainfellner JA, Brain Pathol, 5, 201 (1995)
  17. Hansen L. A., Masliah E., Terry R. D., Mirra S. S., A neuropathological subset of Alzheimer's disease with concomitant Lewy body disease and spongiform change, 10.1007/bf00688209
  18. Hsiao K., Prusiner S. B., Inherited human prion diseases, 10.1212/wnl.40.12.1820
  19. Ikeda S., Yanagisawa Nobuo, Allsop David, Glenner George G., Gerstmann-Str�ussler-Scheinker disease showing b-protein type cerebellar and cerebral amyloid angiopathy, 10.1007/s004010050158
  20. 20. T Kitamoto, and J Tateishi (1994 ) Human prion diseases with variant prion protein . Phil Trans Roy SocLondonB 343 : 391 -398 .
  21. Kitamoto T, Am J Pathol, 131, 435 (1988)
  22. Kitamoto T, Am J Pathol, 140, 1285 (1992)
  23. Kitamoto T, Alzheimer's Disease: Advances in Clinical and Basic Research, 469 (1993)
  24. Kretzschmar HansA., Honold Georg, Seitelberger Franz, Feucht M., Wessely P., Mehraein Parviz, Budka Herbert, Prion protein mutation in family first reported by Gerstmann, Sträussler, and Scheinker, 10.1016/0140-6736(91)92826-n
  25. Lantos Peter L., McGill Iain S., Janota Ivan, Doey Lawrence J., Collinge John, Bruce Mary T., Whatley Stephen A., Anderton Brian H., Clinton Joanne, Roberts Gareth W., Rossor Martin N., Prion protein immunocytochemistry helps to establish the true incidence of prion diseases, 10.1016/0304-3940(92)90776-4
  26. Liberski PP, Light and Electron Microscopic Neuropathology of Slow Virus Disorders, 111 (1993)
  27. Liberski PP, Light and Electron Microscopic Neuropathology of Slow Virus Disorders, 373 (1993)
  28. Miyazono M., Kitamoto T., Iwaki T., Tateishi J., Colocalization of prion protein and ? protein in the same amyloid plaques in patients with Gerstmann-Str�ussler Syndrome, 10.1007/bf00713522
  29. Mizutani T, J Neurol Neurosurg Psychiat, 44, 103 (1981)
  30. Nochlin D., Sumi S. M., Bird T. D., Snow A. D., Leventhal C. M., Beyreuther K., Masters C.L., Familial dementia with PrP-positive amyloid plaques: A variant of Gerstmann-Straussler syndrome, 10.1212/wnl.39.7.910
  31. Pollanen M.S., Bergeron C., Weyer L., Absence of protease-resistant prion protein in dementia characterized by neuronal loss and status spongiosus, 10.1007/bf00228588
  32. Prusiner Stanley B., Hsiao Karen K., Human prion diseases, 10.1002/ana.410350404
  33. Ribadeau-Dumas JL, Neurology, 316 (1974)
  34. Richardson EP, Brain Pathol, 5, 33 (1995)
  35. Shin R, Lab Invest, 64, 693 (1991)
  36. Tateishi J, Brain Pathol, 5, 53 (1995)
  37. Weller RO, Neuropathol Appl Neurobiol, 12, 117 (1986)
  38. Will R.G., Diringer H., Bridges LeslieR., Fraser H., Hardy John, Goate Alison, Arya S.C., Prion disease, 10.1016/0140-6736(90)91907-r