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Prion diseases.
McKintosh E, Tabrizi SJ, Collinge J. McKintosh E, et al. Among authors: collinge j. J Neurovirol. 2003 Apr;9(2):183-93. doi: 10.1080/13550280390194082. J Neurovirol. 2003. PMID: 12707849 Review.
Human prion diseases.
Palmer MS, Collinge J. Palmer MS, et al. Among authors: collinge j. Curr Opin Neurol Neurosurg. 1992 Dec;5(6):895-901. Curr Opin Neurol Neurosurg. 1992. PMID: 1467584 Review.
Prion diseases.
Collinge J, Palmer MS. Collinge J, et al. Curr Opin Genet Dev. 1992 Jun;2(3):448-54. doi: 10.1016/s0959-437x(05)80156-x. Curr Opin Genet Dev. 1992. PMID: 1504620 Review.
Molecular genetics of human prion diseases.
Collinge J, Palmer MS. Collinge J, et al. Philos Trans R Soc Lond B Biol Sci. 1994 Mar 29;343(1306):371-8. doi: 10.1098/rstb.1994.0031. Philos Trans R Soc Lond B Biol Sci. 1994. PMID: 7913754 Review.
Human prion diseases.
Collinge J, Palmer MS. Collinge J, et al. Baillieres Clin Neurol. 1994 Aug;3(2):241-7. Baillieres Clin Neurol. 1994. PMID: 7952846 Review. No abstract available.
Prion protein is necessary for normal synaptic function.
Collinge J, Whittington MA, Sidle KC, Smith CJ, Palmer MS, Clarke AR, Jefferys JG. Collinge J, et al. Nature. 1994 Jul 28;370(6487):295-7. doi: 10.1038/370295a0. Nature. 1994. PMID: 8035877
512 results