Mead S - Search Results

1

Characterization of Prion Disease Associated with a Two-Octapeptide Repeat Insertion.

Brennecke N, Cali I, Mok TH, Speedy H, Genomics England Research Consortium, Hosszu LLP, Stehmann C, Cracco L, Puoti G, Prior TW, Cohen ML, Collins SJ, Mead S, Appleby BS. Brennecke N, et al. Among authors: mead s. Viruses. 2021 Sep 8;13(9):1794. doi: 10.3390/v13091794. Viruses. 2021. PMID: 34578375 Free PMC article.

2

Examination of the human prion protein-like gene doppel for genetic susceptibility to sporadic and variant Creutzfeldt-Jakob disease.

Mead S, Beck J, Dickinson A, Fisher EM, Collinge J. Mead S, et al. Neurosci Lett. 2000 Aug 25;290(2):117-20. doi: 10.1016/s0304-3940(00)01319-7. Neurosci Lett. 2000. PMID: 10936691

3

Two-octapeptide repeat deletion of prion protein associated with rapidly progressive dementia.

Beck JA, Mead S, Campbell TA, Dickinson A, Wientjens DP, Croes EA, Van Duijn CM, Collinge J. Beck JA, et al. Among authors: mead s. Neurology. 2001 Jul 24;57(2):354-6. doi: 10.1212/wnl.57.2.354. Neurology. 2001. PMID: 11468331

4

Prion disease genetics.

Mead S. Mead S. Eur J Hum Genet. 2006 Mar;14(3):273-81. doi: 10.1038/sj.ejhg.5201544. Eur J Hum Genet. 2006. PMID: 16391566 Review.

5

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

6

Inherited prion disease with 5-OPRI: phenotype modification by repeat length and codon 129.

Mead S, Webb TE, Campbell TA, Beck J, Linehan JM, Rutherfoord S, Joiner S, Wadsworth JD, Heckmann J, Wroe S, Doey L, King A, Collinge J. Mead S, et al. Neurology. 2007 Aug 21;69(8):730-8. doi: 10.1212/01.wnl.0000267642.41594.9d. Neurology. 2007. PMID: 17709704

7

Creutzfeldt-Jakob disease, prion protein gene codon 129VV, and a novel PrPSc type in a young British woman.

Mead S, Joiner S, Desbruslais M, Beck JA, O'Donoghue M, Lantos P, Wadsworth JD, Collinge J. Mead S, et al. Arch Neurol. 2007 Dec;64(12):1780-4. doi: 10.1001/archneur.64.12.1780. Arch Neurol. 2007. PMID: 18071044

8

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: mead s. Methods Mol Biol. 2008;459:197-227. doi: 10.1007/978-1-59745-234-2_14. Methods Mol Biol. 2008. PMID: 18576157

9

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. Among authors: mead s. J Neuropathol Exp Neurol. 2008 Sep;67(9):838-41. doi: 10.1097/NEN.0b013e318182f36e. J Neuropathol Exp Neurol. 2008. PMID: 18716560

10

Age of onset and death in inherited prion disease are heritable.

Webb TE, Whittaker J, Collinge J, Mead S. Webb TE, et al. Among authors: mead s. Am J Med Genet B Neuropsychiatr Genet. 2009 Jun 5;150B(4):496-501. doi: 10.1002/ajmg.b.30844. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 18729123

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