Istraživanje humanih prion bolesti i mogućosti rane dijagnostike nove varijante Creutzfeldt-Jakobove bolesti (nv CJB)
DOI:
https://doi.org/10.5644/Radovi.329Abstract
No abstract available.
References
Collinge, J., Sidle, K. C. L., Meads, J., Ironside, J., & Hill, A. F. (1996). Molecular analysis of prion strain variation and the aetiology of “new variant” CJD. Nature, 383, 685–690.
Fischer, M. B., Roeckl, C., Parizek, P., Schwarz, H. P., & Aguzzi, A. (2000). Binding of disease-associated prion protein to plasminogen. Nature Medicine, 6, 479–483.
Fournier, J. G., Kopp, N., Streichenberger, N., Escaig-Haye, F., Langeveld, J., & Brown, P. (2000). Electron microscopy of brain amyloid plaques from a patient with nvCJD. Acta Neuropathologica, 99, 637–642.
Kretzschmar, H. A., Ironside, J. W., DeArmond, S. J., & Tateishi, J. (1996). Diagnostic criteria for sporadic Creutzfeldt-Jakob disease. Archives of Neurology, 53, 913–920.
Prusiner, S. B., Collinge, J., Powell, J., & Anderton, B. (1992). Prion diseases of humans and animals. New York: Ellis Horwood.
Prusiner, S. B. (1991). Molecular biology of prion diseases. Science, 252, 1515–1522.
Sutherland, K., Barrie, C., & Ironside, J. W. (1994). Automatic quantification of amyloid plaque formation in human spongiform encephalopathy. Neurodegeneration, 3, 293–300.
Windl, O., Giese, A., Schulz-Schaeffer, W., Zerr, I., Skworc, K., Arendt, S., Oberdieck, C., Bodemer, M., Poser, S., & Kretzschmar, H. A. (1999). Molecular genetics of human prion diseases in Germany. Human Genetics, 105, 244–252.
Downloads
Published
Issue
Section
License
Copyright (c) 2026 Đemo Subašić
This work is licensed under a Creative Commons Attribution 4.0 International License.
