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Page 1
Human prion diseases.
Palmer MS, Collinge J. Palmer MS, et al. Among authors: collinge j. Baillieres Clin Neurol. 1992 Nov;1(3):627-51. Baillieres Clin Neurol. 1992. PMID: 1344206 Review. No abstract available.
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.
Prion dementia without characteristic pathology.
Collinge J, Owen F, Poulter M, Leach M, Crow TJ, Rossor MN, Hardy J, Mullan MJ, Janota I, Lantos PL. Collinge J, et al. Lancet. 1990 Jul 7;336(8706):7-9. doi: 10.1016/0140-6736(90)91518-f. Lancet. 1990. PMID: 1973256
Insertion in prion protein gene in familial Creutzfeldt-Jakob disease.
Owen F, Poulter M, Lofthouse R, Collinge J, Crow TJ, Risby D, Baker HF, Ridley RM, Hsiao K, Prusiner SB. Owen F, et al. Among authors: collinge j. Lancet. 1989 Jan 7;1(8628):51-2. doi: 10.1016/s0140-6736(89)91713-3. Lancet. 1989. PMID: 2563037 No abstract available.
Sporadic Creutzfeldt-Jakob disease in a 16-year-old in the UK.
Britton TC, al-Sarraj S, Shaw C, Campbell T, Collinge J. Britton TC, et al. Among authors: collinge j. Lancet. 1995 Oct 28;346(8983):1155. doi: 10.1016/s0140-6736(95)91827-2. Lancet. 1995. PMID: 7475611 No abstract available.
516 results