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Page 1
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 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
Prion dementia.
Collinge J, Palmer MS, Rossor MN, Janota I, Lantos PL. Collinge J, et al. Lancet. 1993 Mar 6;341(8845):627; author reply 627-8. Lancet. 1993. PMID: 8094847 No abstract available.
Familial non-specific dementia maps to chromosome 3.
Brown J, Ashworth A, Gydesen S, Sorensen A, Rossor M, Hardy J, Collinge J. Brown J, et al. Among authors: collinge j. Hum Mol Genet. 1995 Sep;4(9):1625-8. doi: 10.1093/hmg/4.9.1625. Hum Mol Genet. 1995. PMID: 8541850
A new variant of prion disease.
Collinge J, Rossor M. Collinge J, et al. Lancet. 1996 Apr 6;347(9006):916-7. doi: 10.1016/s0140-6736(96)91407-5. Lancet. 1996. PMID: 8598749 No abstract available.
516 results