Träfflista för sökning "WFRF:(Traynor Bryan J) srt2:(2010-2014);pers:(Passant Ulla)"

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1.	Englund, Elisabet, et al. (author) Familial Lund frontotemporal dementia caused by C9ORF72 hexanucleotide expansion. 2012 In: Neurobiology of Aging. - : Elsevier BV. - 1558-1497 .- 0197-4580. Journal article (peer-reviewed)abstract Frontotemporal dementia (FTD) as an important clinical entity was rediscovered in Lund and Manchester in the early 1990s. Here we show that the large Lund pedigree with behavioral variant of frontotemporal dementia previously described with this disorder has an expansion in the recently described C9ORF72 locus on chromosome 9.
2.	Landqvist, Maria, et al. (author) Frontotemporal dementia with a C9ORF72 expansion in a Swedish family: clinical and neuropathological characteristics. 2013 In: American Journal of Neurodegenerative Disease. - 2165-591X. ; 2:4, s. 276-286 Journal article (peer-reviewed)abstract In 2011 the C9ORF72 repeat expansion was identified as the most frequent genetic mutation underlying FTD and ALS. The main aim of this study was to investigate clinical characteristics in a large C9ORF72-positive FTD family, and to compare these with the neuropathological findings.

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Author/Editor: Englund, Elisabet (2); Gustafson, Lars (2); Passant, Ulla (2)Undo refine; Traynor, Bryan J (2); Renton, Alan E (2); Hardy, John (1); show more...; Nilsson, Karin (1); Rohrer, Jonathan D (1); Majounie, Elisa (1); Mok, Kin (1); Landqvist, Maria (1); show less...

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