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Page 1
Serum neurofilament light chain protein is a measure of disease intensity in frontotemporal dementia.
Rohrer JD, Woollacott IO, Dick KM, Brotherhood E, Gordon E, Fellows A, Toombs J, Druyeh R, Cardoso MJ, Ourselin S, Nicholas JM, Norgren N, Mead S, Andreasson U, Blennow K, Schott JM, Fox NC, Warren JD, Zetterberg H. Rohrer JD, et al. Among authors: mead s. Neurology. 2016 Sep 27;87(13):1329-36. doi: 10.1212/WNL.0000000000003154. Epub 2016 Aug 31. Neurology. 2016. PMID: 27581216 Free PMC article.
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.
Mapping the progression of progranulin-associated frontotemporal lobar degeneration.
Rohrer JD, Warren JD, Barnes J, Mead S, Beck J, Pepple T, Boyes R, Omar R, Collinge J, Stevens JM, Warrington EK, Rossor MN, Fox NC. Rohrer JD, et al. Among authors: mead s. Nat Clin Pract Neurol. 2008 Aug;4(8):455-60. doi: 10.1038/ncpneuro0869. Epub 2008 Jul 22. Nat Clin Pract Neurol. 2008. PMID: 18648346 Free PMC article.
Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series.
Webb TE, Poulter M, Beck J, Uphill J, Adamson G, Campbell T, Linehan J, Powell C, Brandner S, Pal S, Siddique D, Wadsworth JD, Joiner S, Alner K, Petersen C, Hampson S, Rhymes C, Treacy C, Storey E, Geschwind MD, Nemeth AH, Wroe S, Collinge J, Mead S. Webb TE, et al. Among authors: mead s. Brain. 2008 Oct;131(Pt 10):2632-46. doi: 10.1093/brain/awn202. Epub 2008 Aug 30. Brain. 2008. PMID: 18757886 Free PMC article.
461 results