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Clinicopathological features of familial Alzheimer's disease associated with the M139V mutation in the presenilin 1 gene. Pedigree but not mutation specific age at onset provides evidence for a further genetic factor.
Fox NC, Kennedy AM, Harvey RJ, Lantos PL, Roques PK, Collinge J, Hardy J, Hutton M, Stevens JM, Warrington EK, Rossor MN. Fox NC, et al. Among authors: collinge j. Brain. 1997 Mar;120 ( Pt 3):491-501. doi: 10.1093/brain/120.3.491. Brain. 1997. PMID: 9126060
Insertions in the prion protein gene in atypical dementias.
Owen F, Poulter M, Collinge J, Leach M, Shah T, Lofthouse R, Chen YF, Crow TJ, Harding AE, Hardy J, et al. Owen F, et al. Among authors: collinge j. Exp Neurol. 1991 May;112(2):240-2. doi: 10.1016/0014-4886(91)90075-n. Exp Neurol. 1991. PMID: 1674696
Genetic characterization of a novel familial dementia.
Brown J, Smith S, Brun A, Collinge J, Gydesen S, Hardy J, Mullan M, Goate A. Brown J, et al. Among authors: collinge j. Ann N Y Acad Sci. 1991;640:181-3. doi: 10.1111/j.1749-6632.1991.tb00213.x. Ann N Y Acad Sci. 1991. PMID: 1776737
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
Transmission of fatal familial insomnia to laboratory animals.
Collinge J, Palmer MS, Sidle KC, Gowland I, Medori R, Ironside J, Lantos P. Collinge J, et al. Lancet. 1995 Aug 26;346(8974):569-70. doi: 10.1016/s0140-6736(95)91405-6. Lancet. 1995. PMID: 7658786 No abstract available.
516 results