Collinge J - Search Results

1

Iatrogenic CJD due to pituitary-derived growth hormone with genetically determined incubation times of up to 40 years.

Rudge P, Jaunmuktane Z, Adlard P, Bjurstrom N, Caine D, Lowe J, Norsworthy P, Hummerich H, Druyeh R, Wadsworth JD, Brandner S, Hyare H, Mead S, Collinge J. Rudge P, et al. Among authors: collinge j. Brain. 2015 Nov;138(Pt 11):3386-99. doi: 10.1093/brain/awv235. Epub 2015 Aug 11. Brain. 2015. PMID: 26268531 Free PMC article.

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

Tissue handling in suspected Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases).

Budka H, Aguzzi A, Brown P, Brucher JM, Bugiani O, Collinge J, Diringer H, Gullotta F, Haltia M, Hauw JJ. Budka H, et al. Among authors: collinge j. Brain Pathol. 1995 Jul;5(3):319-22. doi: 10.1111/j.1750-3639.1995.tb00609.x. Brain Pathol. 1995. PMID: 8520732 Review.

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

Molecular biology of prion propagation.

Wadsworth JD, Jackson GS, Hill AF, Collinge J. Wadsworth JD, et al. Among authors: collinge j. Curr Opin Genet Dev. 1999 Jun;9(3):338-45. doi: 10.1016/s0959-437x(99)80051-3. Curr Opin Genet Dev. 1999. PMID: 10377292 Review.

9

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

10

Strain-specific prion-protein conformation determined by metal ions.

Wadsworth JD, Hill AF, Joiner S, Jackson GS, Clarke AR, Collinge J. Wadsworth JD, et al. Among authors: collinge j. Nat Cell Biol. 1999 May;1(1):55-9. doi: 10.1038/9030. Nat Cell Biol. 1999. PMID: 10559865

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