Collinge J - Search Results

1

Familial Alzheimer's disease and inherited prion disease in the UK are poorly ascertained.

Stevens JC, Beck J, Lukic A, Ryan N, Abbs S, Collinge J, Fox NC, Mead S. Stevens JC, et al. Among authors: collinge j. J Neurol Neurosurg Psychiatry. 2011 Sep;82(9):1054-7. doi: 10.1136/jnnp.2009.199653. Epub 2010 Aug 27. J Neurol Neurosurg Psychiatry. 2011. PMID: 20802216

2

Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features.

Collinge J, Brown J, Hardy J, Mullan M, Rossor MN, Baker H, Crow TJ, Lofthouse R, Poulter M, Ridley R, et al. Collinge J, et al. Brain. 1992 Jun;115 ( Pt 3):687-710. doi: 10.1093/brain/115.3.687. Brain. 1992. PMID: 1352725

3

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.

4

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.

5

Human prion diseases.

Collinge J, Palmer MS. Collinge J, et al. Baillieres Clin Neurol. 1994 Aug;3(2):241-7. Baillieres Clin Neurol. 1994. PMID: 7952846 Review. No abstract available.

6

Inherited prion diseases.

Collinge J. Collinge J. Adv Neurol. 1993;61:155-65. Adv Neurol. 1993. PMID: 8421966 Review. No abstract available.

7

A prion disease with a novel 96-base pair insertional mutation in the prion protein gene.

Campbell TA, Palmer MS, Will RG, Gibb WR, Luthert PJ, Collinge J. Campbell TA, et al. Among authors: collinge j. Neurology. 1996 Mar;46(3):761-6. doi: 10.1212/wnl.46.3.761. Neurology. 1996. PMID: 8618679

8

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: collinge j. Lancet. 1996 Jun 1;347(9014):1560. doi: 10.1016/s0140-6736(96)90715-1. Lancet. 1996. PMID: 8684135 No abstract available.

9

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. Lancet. 1996 Jul 6;348(9019):56. doi: 10.1016/s0140-6736(05)64378-4. Lancet. 1996. PMID: 8691941 No abstract available.

10

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

512 results

Search Page