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TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration.
Wils H, Kleinberger G, Janssens J, Pereson S, Joris G, Cuijt I, Smits V, Ceuterick-de Groote C, Van Broeckhoven C, Kumar-Singh S. Wils H, et al. Among authors: van broeckhoven c. Proc Natl Acad Sci U S A. 2010 Feb 23;107(8):3858-63. doi: 10.1073/pnas.0912417107. Epub 2010 Feb 3. Proc Natl Acad Sci U S A. 2010. PMID: 20133711 Free PMC article.
Dense-core senile plaques in the Flemish variant of Alzheimer's disease are vasocentric.
Kumar-Singh S, Cras P, Wang R, Kros JM, van Swieten J, Lübke U, Ceuterick C, Serneels S, Vennekens K, Timmermans JP, Van Marck E, Martin JJ, van Duijn CM, Van Broeckhoven C. Kumar-Singh S, et al. Among authors: van swieten j, van duijn cm, van marck e, van broeckhoven c. Am J Pathol. 2002 Aug;161(2):507-20. doi: 10.1016/S0002-9440(10)64207-1. Am J Pathol. 2002. PMID: 12163376 Free PMC article.
A novel presenilin 1 mutation associated with Pick's disease but not beta-amyloid plaques.
Dermaut B, Kumar-Singh S, Engelborghs S, Theuns J, Rademakers R, Saerens J, Pickut BA, Peeters K, van den Broeck M, Vennekens K, Claes S, Cruts M, Cras P, Martin JJ, Van Broeckhoven C, De Deyn PP. Dermaut B, et al. Among authors: van den broeck m, van broeckhoven c. Ann Neurol. 2004 May;55(5):617-26. doi: 10.1002/ana.20083. Ann Neurol. 2004. PMID: 15122701
Tau is central in the genetic Alzheimer-frontotemporal dementia spectrum.
Dermaut B, Kumar-Singh S, Rademakers R, Theuns J, Cruts M, Van Broeckhoven C. Dermaut B, et al. Among authors: van broeckhoven c. Trends Genet. 2005 Dec;21(12):664-72. doi: 10.1016/j.tig.2005.09.005. Epub 2005 Oct 10. Trends Genet. 2005. PMID: 16221505 Review.
Characterization of ubiquitinated intraneuronal inclusions in a novel Belgian frontotemporal lobar degeneration family.
Pirici D, Vandenberghe R, Rademakers R, Dermaut B, Cruts M, Vennekens K, Cuijt I, Lübke U, Ceuterick C, Martin JJ, Van Broeckhoven C, Kumar-Singh S. Pirici D, et al. Among authors: van broeckhoven c. J Neuropathol Exp Neurol. 2006 Mar;65(3):289-301. doi: 10.1097/01.jnen.0000205147.39210.c7. J Neuropathol Exp Neurol. 2006. PMID: 16651890
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21.
Cruts M, Gijselinck I, van der Zee J, Engelborghs S, Wils H, Pirici D, Rademakers R, Vandenberghe R, Dermaut B, Martin JJ, van Duijn C, Peeters K, Sciot R, Santens P, De Pooter T, Mattheijssens M, Van den Broeck M, Cuijt I, Vennekens K, De Deyn PP, Kumar-Singh S, Van Broeckhoven C. Cruts M, et al. Among authors: van den broeck m, van der zee j, van duijn c, van broeckhoven c. Nature. 2006 Aug 24;442(7105):920-4. doi: 10.1038/nature05017. Epub 2006 Jul 16. Nature. 2006. PMID: 16862115
776 results