Beck J - Search Results

1

Incomplete penetrance of familial Alzheimer's disease in a pedigree with a novel presenilin-1 gene mutation.

Rossor MN, Fox NC, Beck J, Campbell TC, Collinge J. Rossor MN, et al. Among authors: beck j. Lancet. 1996 Jun 1;347(9014):1560. doi: 10.1016/s0140-6736(96)90715-1. Lancet. 1996. PMID: 8684135 No abstract available.

2

Clinical phenotype and genetic associations in autosomal dominant familial Alzheimer's disease: a case series.

Ryan NS, Nicholas JM, Weston PSJ, Liang Y, Lashley T, Guerreiro R, Adamson G, Kenny J, Beck J, Chavez-Gutierrez L, de Strooper B, Revesz T, Holton J, Mead S, Rossor MN, Fox NC. Ryan NS, et al. Among authors: beck j. Lancet Neurol. 2016 Dec;15(13):1326-1335. doi: 10.1016/S1474-4422(16)30193-4. Epub 2016 Oct 21. Lancet Neurol. 2016. PMID: 27777022 Free article.

3

Early onset familial Alzheimer's disease: Mutation frequency in 31 families.

Janssen JC, Beck JA, Campbell TA, Dickinson A, Fox NC, Harvey RJ, Houlden H, Rossor MN, Collinge J. Janssen JC, et al. Among authors: beck ja. Neurology. 2003 Jan 28;60(2):235-9. doi: 10.1212/01.wnl.0000042088.22694.e3. Neurology. 2003. PMID: 12552037

4

A presenilin 1 R278I mutation presenting with language impairment.

Godbolt AK, Beck JA, Collinge J, Garrard P, Warren JD, Fox NC, Rossor MN. Godbolt AK, et al. Among authors: beck ja. Neurology. 2004 Nov 9;63(9):1702-4. doi: 10.1212/01.wnl.0000143060.98164.1a. Neurology. 2004. PMID: 15534260

5

Pathogenic presenilin 1 mutations (P436S & I143F) in early-onset Alzheimer's disease in the UK. Mutations in brief no. 223. Online.

Palmer MS, Beck JA, Campbell TA, Humphries CB, Roques PK, Fox NC, Harvey R, Rossor MN, Collinge J. Palmer MS, et al. Among authors: beck ja. Hum Mutat. 1999;13(3):256. doi: 10.1002/(sici)1098-1004(1999)13:3<256::aid-humu11>3.0.co;2-p. Hum Mutat. 1999. PMID: 10090481

6

Prion protein gene analysis in new variant cases of Creutzfeldt-Jakob disease.

Collinge J, Beck J, Campbell T, Estibeiro K, Will RG. Collinge J, et al. Among authors: beck j. Lancet. 1996 Jul 6;348(9019):56. doi: 10.1016/s0140-6736(05)64378-4. Lancet. 1996. PMID: 8691941 No abstract available.

7

Alzheimer's disease due to an intronic presenilin-1 (PSEN1 intron 4) mutation: A clinicopathological study.

Janssen JC, Hall M, Fox NC, Harvey RJ, Beck J, Dickinson A, Campbell T, Collinge J, Lantos PL, Cipolotti L, Stevens JM, Rossor MN. Janssen JC, et al. Among authors: beck j. Brain. 2000 May;123 ( Pt 5):894-907. doi: 10.1093/brain/123.5.894. Brain. 2000. PMID: 10775535

8

Autopsy-confirmed familial early-onset Alzheimer disease caused by the l153V presenilin 1 mutation.

Janssen JC, Lantos PL, Fox NC, Harvey RJ, Beck J, Dickinson A, Campbell TA, Collinge J, Hanger DP, Cipolotti L, Stevens JM, Rossor MN. Janssen JC, et al. Among authors: beck j. Arch Neurol. 2001 Jun;58(6):953-8. doi: 10.1001/archneur.58.6.953. Arch Neurol. 2001. PMID: 11405810

9

A novel presenilin 1 deletion (p.L166del) associated with early onset familial Alzheimer's disease.

Knight WD, Kennedy J, Mead S, Rossor MN, Beck J, Collinge J, Mummery C. Knight WD, et al. Among authors: beck j. Eur J Neurol. 2007 Jul;14(7):829-31. doi: 10.1111/j.1468-1331.2007.01857.x. Eur J Neurol. 2007. PMID: 17594345

10

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. 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.

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