Mead S - Search Results

1

Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration.

Rohrer JD, Lashley T, Schott JM, Warren JE, Mead S, Isaacs AM, Beck J, Hardy J, de Silva R, Warrington E, Troakes C, Al-Sarraj S, King A, Borroni B, Clarkson MJ, Ourselin S, Holton JL, Fox NC, Revesz T, Rossor MN, Warren JD. Rohrer JD, et al. Among authors: mead s. Brain. 2011 Sep;134(Pt 9):2565-81. doi: 10.1093/brain/awr198. Brain. 2011. PMID: 21908872 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

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

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

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

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.

7

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

8

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

9

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

10

A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series.

Beck J, Rohrer JD, Campbell T, Isaacs A, Morrison KE, Goodall EF, Warrington EK, Stevens J, Revesz T, Holton J, Al-Sarraj S, King A, Scahill R, Warren JD, Fox NC, Rossor MN, Collinge J, Mead S. Beck J, et al. Among authors: mead s. Brain. 2008 Mar;131(Pt 3):706-20. doi: 10.1093/brain/awm320. Epub 2008 Jan 29. Brain. 2008. PMID: 18234697 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

455 results

Search Page