Campbell T - Search Results

1

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

2

Sporadic Creutzfeldt-Jakob disease in a 16-year-old in the UK.

Britton TC, al-Sarraj S, Shaw C, Campbell T, Collinge J. Britton TC, et al. Among authors: campbell t. Lancet. 1995 Oct 28;346(8983):1155. doi: 10.1016/s0140-6736(95)91827-2. Lancet. 1995. PMID: 7475611 No abstract available.

3

G/T polymorphism in CRYA2 gene.

Ashworth A, Campbell T, Palmer M, Collinge J, Brown J. Ashworth A, et al. Among authors: campbell t. Hum Mol Genet. 1994 Sep;3(9):1712. doi: 10.1093/hmg/3.9.1712. Hum Mol Genet. 1994. PMID: 7833944 No abstract available.

4

Familial Pick's disease and dementia in frontal lobe degeneration of non-Alzheimer type are not variants of prion disease.

Collinge J, Palmer MS, Sidle KC, Mahal SP, Campbell T, Brown J, Hardy J, Brun AE, Gustafson L, Bakker E, et al. Collinge J, et al. Among authors: campbell t. J Neurol Neurosurg Psychiatry. 1994 Jun;57(6):762. doi: 10.1136/jnnp.57.6.762. J Neurol Neurosurg Psychiatry. 1994. PMID: 8006666 Free PMC article. No abstract available.

5

Deletions in the prion protein gene are not associated with CJD.

Palmer MS, Mahal SP, Campbell TA, Hill AF, Sidle KC, Laplanche JL, Collinge J. Palmer MS, et al. Among authors: campbell ta. Hum Mol Genet. 1993 May;2(5):541-4. doi: 10.1093/hmg/2.5.541. Hum Mol Genet. 1993. PMID: 8100163

6

Inherited prion disease (PrP lysine 200) in Britain: two case reports.

Collinge J, Palmer MS, Campbell T, Sidle KC, Carroll D, Harding A. Collinge J, et al. Among authors: campbell t. BMJ. 1993 Jan 30;306(6873):301-2. doi: 10.1136/bmj.306.6873.301. BMJ. 1993. PMID: 8461647 Free PMC article.

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. Neurology. 1996 Mar;46(3):761-6. doi: 10.1212/wnl.46.3.761. Neurology. 1996. PMID: 8618679

8

Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene.

Windl O, Dempster M, Estibeiro JP, Lathe R, de Silva R, Esmonde T, Will R, Springbett A, Campbell TA, Sidle KC, Palmer MS, Collinge J. Windl O, et al. Among authors: campbell ta. Hum Genet. 1996 Sep;98(3):259-64. doi: 10.1007/s004390050204. Hum Genet. 1996. PMID: 8707291

9

Sequence variation in intron of prion protein gene, crucial for complete diagnostic strategies.

Palmer MS, van Leeven RH, Mahal SP, Campbell TA, Humphreys CB, Collinge J. Palmer MS, et al. Among authors: campbell ta. Hum Mutat. 1996;7(3):280-1. doi: 10.1002/(SICI)1098-1004(1996)7:3<280::AID-HUMU17>3.0.CO;2-Z. Hum Mutat. 1996. PMID: 8829666 No abstract available.

10

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: campbell ta. 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

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