Collinge J - Search Results

1

MRI findings are often missed in the diagnosis of Creutzfeldt-Jakob disease.

Carswell C, Thompson A, Lukic A, Stevens J, Rudge P, Mead S, Collinge J, Hyare H. Carswell C, et al. Among authors: collinge j. BMC Neurol. 2012 Dec 5;12:153. doi: 10.1186/1471-2377-12-153. BMC Neurol. 2012. PMID: 23216655 Free PMC article.

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

Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease.

Collinge J, Palmer MS, Dryden AJ. Collinge J, et al. Lancet. 1991 Jun 15;337(8755):1441-2. doi: 10.1016/0140-6736(91)93128-v. Lancet. 1991. PMID: 1675319

4

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt-Jakob disease.

Palmer MS, Dryden AJ, Hughes JT, Collinge J. Palmer MS, et al. Among authors: collinge j. Nature. 1991 Jul 25;352(6333):340-2. doi: 10.1038/352340a0. Nature. 1991. PMID: 1677164

5

Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein.

Telling GC, Scott M, Hsiao KK, Foster D, Yang SL, Torchia M, Sidle KC, Collinge J, DeArmond SJ, Prusiner SB. Telling GC, et al. Among authors: collinge j. Proc Natl Acad Sci U S A. 1994 Oct 11;91(21):9936-40. doi: 10.1073/pnas.91.21.9936. Proc Natl Acad Sci U S A. 1994. PMID: 7937921 Free PMC article.

6

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

7

Diagnosis of new variant Creutzfeldt-Jakob disease by tonsil biopsy.

Hill AF, Zeidler M, Ironside J, Collinge J. Hill AF, et al. Among authors: collinge j. Lancet. 1997 Jan 11;349(9045):99-100. doi: 10.1016/S0140-6736(97)24002-X. Lancet. 1997. PMID: 8996424 No abstract available.

8

Peripheral neuropathy in Creutzfeldt-Jakob disease.

Esiri MM, Gordon WI, Collinge J, Patten JS. Esiri MM, et al. Among authors: collinge j. Neurology. 1997 Mar;48(3):784. doi: 10.1212/wnl.48.3.784. Neurology. 1997. PMID: 9065568 No abstract available.

9

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

10

Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples.

Hill AF, Butterworth RJ, Joiner S, Jackson G, Rossor MN, Thomas DJ, Frosh A, Tolley N, Bell JE, Spencer M, King A, Al-Sarraj S, Ironside JW, Lantos PL, Collinge J. Hill AF, et al. Among authors: collinge j. Lancet. 1999 Jan 16;353(9148):183-9. doi: 10.1016/s0140-6736(98)12075-5. Lancet. 1999. PMID: 9923873

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