Collinge J - Search Results

1

Type of prion protein in UK farmers with Creutzfeldt-Jakob disease.

Hill AF, Will RG, Ironside J, Collinge J. Hill AF, et al. Among authors: collinge j. Lancet. 1997 Jul 19;350(9072):188. doi: 10.1016/S0140-6736(05)62356-2. Lancet. 1997. PMID: 9250195 No abstract available.

2

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.

3

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.

4

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

5

Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assay.

Wadsworth JD, Joiner S, Hill AF, Campbell TA, Desbruslais M, Luthert PJ, Collinge J. Wadsworth JD, et al. Among authors: collinge j. Lancet. 2001 Jul 21;358(9277):171-80. doi: 10.1016/s0140-6736(01)05403-4. Lancet. 2001. PMID: 11476832

6

Molecular classification of sporadic Creutzfeldt-Jakob disease.

Hill AF, Joiner S, Wadsworth JD, Sidle KC, Bell JE, Budka H, Ironside JW, Collinge J. Hill AF, et al. Among authors: collinge j. Brain. 2003 Jun;126(Pt 6):1333-46. doi: 10.1093/brain/awg125. Brain. 2003. PMID: 12764055

7

[Consensus report: tissue handling in suspected Creutzfeldt-Jakob disease and other spongiform encephalopathies (prion diseases) in the human. European Union Biomed-1 Concerted Action].

Budka H, Aguzzi A, Brown P, Brucher JM, Bugiani O, Collinge J, Diringer H, Gullotta F, Haltia M, Hauw JJ, Ironside JW, Kretzschmar HA, Lantos PL, Masullo C, Pocchiari M, Schlote W, Tateishi J, Will RG. Budka H, et al. Among authors: collinge j. Pathologe. 1996 Mar;17(2):171-5. Pathologe. 1996. PMID: 8650149 Review. German.

8

New variant Creutzfeldt-Jakob disease in France.

Deslys JP, Lasmézas CI, Streichenberger N, Hill A, Collinge J, Dormont D, Kopp N. Deslys JP, et al. Among authors: collinge j. Lancet. 1997 Jan 4;349(9044):30-1. doi: 10.1016/s0140-6736(05)62163-0. Lancet. 1997. PMID: 8988126 No abstract available.

9

Subclinical prion infection in humans and animals.

Hill AF, Collinge J. Hill AF, et al. Among authors: collinge j. Br Med Bull. 2003;66:161-70. doi: 10.1093/bmb/66.1.161. Br Med Bull. 2003. PMID: 14522857 Review.

10

Molecular and clinical classification of human prion disease.

Wadsworth JD, Hill AF, Beck JA, Collinge J. Wadsworth JD, et al. Among authors: collinge j. Br Med Bull. 2003;66:241-54. doi: 10.1093/bmb/66.1.241. Br Med Bull. 2003. PMID: 14522862 Review.

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