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Page 1
TREM2 variants in Alzheimer's disease.
Guerreiro R, Wojtas A, Bras J, Carrasquillo M, Rogaeva E, Majounie E, Cruchaga C, Sassi C, Kauwe JS, Younkin S, Hazrati L, Collinge J, Pocock J, Lashley T, Williams J, Lambert JC, Amouyel P, Goate A, Rademakers R, Morgan K, Powell J, St George-Hyslop P, Singleton A, Hardy J; Alzheimer Genetic Analysis Group. Guerreiro R, et al. Among authors: collinge j. N Engl J Med. 2013 Jan 10;368(2):117-27. doi: 10.1056/NEJMoa1211851. Epub 2012 Nov 14. N Engl J Med. 2013. PMID: 23150934 Free PMC article.
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
Sporadic Creutzfeldt-Jakob disease in a 18-year-old in the UK.
Bateman D, Hilton D, Love S, Zeidler M, Beck J, Collinge J. Bateman D, et al. Among authors: collinge j. Lancet. 1995 Oct 28;346(8983):1155-6. doi: 10.1016/s0140-6736(95)91828-0. Lancet. 1995. PMID: 7475612 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