Collinge J - Search Results

1

Cognitive decline heralds onset of symptomatic inherited prion disease.

Mole J, Mead S, Rudge P, Nihat A, Mok T, Collinge J, Caine D. Mole J, et al. Among authors: collinge j. Brain. 2021 Apr 12;144(3):989-998. doi: 10.1093/brain/awaa409. Brain. 2021. PMID: 33844831

2

Inherited prion disease with 144 base pair gene insertion. 1. Genealogical and molecular studies.

Poulter M, Baker HF, Frith CD, Leach M, Lofthouse R, Ridley RM, Shah T, Owen F, Collinge J, Brown J, et al. Poulter M, et al. Among authors: collinge j. Brain. 1992 Jun;115 ( Pt 3):675-85. doi: 10.1093/brain/115.3.675. Brain. 1992. PMID: 1352724

3

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

4

Inherited prion diseases.

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

5

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

6

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

7

Fatal familial insomnia: a new Austrian family.

Almer G, Hainfellner JA, Brücke T, Jellinger K, Kleinert R, Bayer G, Windl O, Kretzschmar HA, Hill A, Sidle K, Collinge J, Budka H. Almer G, et al. Among authors: collinge j. Brain. 1999 Jan;122 ( Pt 1):5-16. doi: 10.1093/brain/122.1.5. Brain. 1999. PMID: 10050890

8

Inherited prion disease with an alanine to valine mutation at codon 117 in the prion protein gene.

Mallucci GR, Campbell TA, Dickinson A, Beck J, Holt M, Plant G, de Pauw KW, Hakin RN, Clarke CE, Howell S, Davies-Jones GA, Lawden M, Smith CM, Ince P, Ironside JW, Bridges LR, Dean A, Weeks I, Collinge J. Mallucci GR, et al. Among authors: collinge j. Brain. 1999 Oct;122 ( Pt 10):1823-37. doi: 10.1093/brain/122.10.1823. Brain. 1999. PMID: 10506086

9

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: collinge j. Brain. 2000 May;123 ( Pt 5):894-907. doi: 10.1093/brain/123.5.894. Brain. 2000. PMID: 10775535

10

Examination of the human prion protein-like gene doppel for genetic susceptibility to sporadic and variant Creutzfeldt-Jakob disease.

Mead S, Beck J, Dickinson A, Fisher EM, Collinge J. Mead S, et al. Among authors: collinge j. Neurosci Lett. 2000 Aug 25;290(2):117-20. doi: 10.1016/s0304-3940(00)01319-7. Neurosci Lett. 2000. PMID: 10936691

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