Mead S - Search Results

1

Genetic analysis of inherited leukodystrophies: genotype-phenotype correlations in the CSF1R gene.

Guerreiro R, Kara E, Le Ber I, Bras J, Rohrer JD, Taipa R, Lashley T, Dupuits C, Gurunlian N, Mochel F, Warren JD, Hannequin D, Sedel F, Depienne C, Camuzat A, Golfier V, Du Boisguéheneuc F, Schottlaender L, Fox NC, Beck J, Mead S, Rossor MN, Hardy J, Revesz T, Brice A, Houlden H. Guerreiro R, et al. Among authors: mead s. JAMA Neurol. 2013 Jul;70(7):875-882. doi: 10.1001/jamaneurol.2013.698. JAMA Neurol. 2013. PMID: 23649896 Free PMC article.

2

Familial British dementia with amyloid angiopathy: early clinical, neuropsychological and imaging findings.

Mead S, James-Galton M, Revesz T, Doshi RB, Harwood G, Pan EL, Ghiso J, Frangione B, Plant G. Mead S, et al. Brain. 2000 May;123 ( Pt 5):975-91. doi: 10.1093/brain/123.5.975. Brain. 2000. PMID: 10775542

3

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

4

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

5

Phenotypic variability in the brains of a family with a prion disease characterized by a 144-base pair insertion in the prion protein gene.

King A, Doey L, Rossor M, Mead S, Collinge J, Lantos P. King A, et al. Among authors: mead s. Neuropathol Appl Neurobiol. 2003 Apr;29(2):98-105. doi: 10.1046/j.1365-2990.2003.00423.x. Neuropathol Appl Neurobiol. 2003. PMID: 12662318

6

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

7

Prion protein (PRNP) genotypes in frontotemporal lobar degeneration syndromes.

Rohrer JD, Mead S, Omar R, Poulter M, Warren JD, Collinge J, Rossor MN. Rohrer JD, et al. Among authors: mead s. Ann Neurol. 2006 Nov;60(5):616. doi: 10.1002/ana.20931. Ann Neurol. 2006. PMID: 16969862 No abstract available.

8

A novel presenilin 1 deletion (p.L166del) associated with early onset familial Alzheimer's disease.

Knight WD, Kennedy J, Mead S, Rossor MN, Beck J, Collinge J, Mummery C. Knight WD, et al. Among authors: mead s. Eur J Neurol. 2007 Jul;14(7):829-31. doi: 10.1111/j.1468-1331.2007.01857.x. Eur J Neurol. 2007. PMID: 17594345

9

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

10

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

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