Beck JA - Search Results

1

Molecular diagnosis of human prion disease.

Wadsworth JD, Powell C, Beck JA, Joiner S, Linehan JM, Brandner S, Mead S, Collinge J. Wadsworth JD, et al. Among authors: beck ja. Methods Mol Biol. 2008;459:197-227. doi: 10.1007/978-1-59745-234-2_14. Methods Mol Biol. 2008. PMID: 18576157

2

PRNP allelic series from 19 years of prion protein gene sequencing at the MRC Prion Unit.

Beck JA, Poulter M, Campbell TA, Adamson G, Uphill JB, Guerreiro R, Jackson GS, Stevens JC, Manji H, Collinge J, Mead S. Beck JA, et al. Hum Mutat. 2010 Jul;31(7):E1551-63. doi: 10.1002/humu.21281. Hum Mutat. 2010. PMID: 20583301

3

Inherited prion disease with six octapeptide repeat insertional mutation--molecular analysis of phenotypic heterogeneity.

Mead S, Poulter M, Beck J, Webb TE, Campbell TA, Linehan JM, Desbruslais M, Joiner S, Wadsworth JD, King A, Lantos P, Collinge J. Mead S, et al. Brain. 2006 Sep;129(Pt 9):2297-317. doi: 10.1093/brain/awl226. Brain. 2006. PMID: 16923955

4

First report of Creutzfeldt-Jakob disease occurring in 2 siblings unexplained by PRNP mutation.

Webb TE, Pal S, Siddique D, Heaney DC, Linehan JM, Wadsworth JD, Joiner S, Beck J, Wroe SJ, Stevenson V, Brandner S, Mead S, Collinge J. Webb TE, et al. J Neuropathol Exp Neurol. 2008 Sep;67(9):838-41. doi: 10.1097/NEN.0b013e318182f36e. J Neuropathol Exp Neurol. 2008. PMID: 18716560

5

Inherited prion disease with 4-octapeptide repeat insertion: disease requires the interaction of multiple genetic risk factors.

Kaski DN, Pennington C, Beck J, Poulter M, Uphill J, Bishop MT, Linehan JM, O'Malley C, Wadsworth JD, Joiner S, Knight RS, Ironside JW, Brandner S, Collinge J, Mead S. Kaski DN, et al. Brain. 2011 Jun;134(Pt 6):1829-38. doi: 10.1093/brain/awr079. Brain. 2011. PMID: 21616973

6

A novel prion disease associated with diarrhea and autonomic neuropathy.

Mead S, Gandhi S, Beck J, Caine D, Gallujipali D, Carswell C, Hyare H, Joiner S, Ayling H, Lashley T, Linehan JM, Al-Doujaily H, Sharps B, Revesz T, Sandberg MK, Reilly MM, Koltzenburg M, Forbes A, Rudge P, Brandner S, Warren JD, Wadsworth JDF, Wood NW, Holton JL, Collinge J. Mead S, et al. N Engl J Med. 2013 Nov 14;369(20):1904-14. doi: 10.1056/NEJMoa1214747. N Engl J Med. 2013. PMID: 24224623 Free PMC article.

7

Predictive testing for inherited prion disease: report of 22 years experience.

Owen J, Beck J, Campbell T, Adamson G, Gorham M, Thompson A, Smithson S, Rosser E, Rudge P, Collinge J, Mead S. Owen J, et al. Eur J Hum Genet. 2014 Dec;22(12):1351-6. doi: 10.1038/ejhg.2014.42. Epub 2014 Apr 9. Eur J Hum Genet. 2014. PMID: 24713662 Free PMC article.

8

Kuru in the 21st century--an acquired human prion disease with very long incubation periods.

Collinge J, Whitfield J, McKintosh E, Beck J, Mead S, Thomas DJ, Alpers MP. Collinge J, et al. Lancet. 2006 Jun 24;367(9528):2068-74. doi: 10.1016/S0140-6736(06)68930-7. Lancet. 2006. PMID: 16798390

9

Molecular and clinical classification of human prion disease.

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

10

Identification and characterization of a novel mouse prion gene allele.

Lloyd SE, Thompson SR, Beck JA, Linehan JM, Wadsworth JD, Brandner S, Collinge J, Fisher EM. Lloyd SE, et al. Among authors: beck ja. Mamm Genome. 2004 May;15(5):383-9. doi: 10.1007/s00335-004-3041-5. Mamm Genome. 2004. PMID: 15170227

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