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Familial early-onset dementia with complex neuropathologic phenotype and genomic background.
Alexander J, Kalev O, Mehrabian S, Traykov L, Raycheva M, Kanakis D, Drineas P, Lutz MI, Ströbel T, Penz T, Schuster M, Bock C, Ferrer I, Paschou P, Kovacs GG. Alexander J, et al. Among authors: strobel t. Neurobiol Aging. 2016 Jun;42:199-204. doi: 10.1016/j.neurobiolaging.2016.03.012. Epub 2016 Mar 21. Neurobiol Aging. 2016. PMID: 27143436
Complement activation in human prion disease.
Kovacs GG, Gasque P, Ströbel T, Lindeck-Pozza E, Strohschneider M, Ironside JW, Budka H, Guentchev M. Kovacs GG, et al. Among authors: strobel t. Neurobiol Dis. 2004 Feb;15(1):21-8. doi: 10.1016/j.nbd.2003.09.010. Neurobiol Dis. 2004. PMID: 14751767
Cathepsin D (C224T) polymorphism in sporadic and genetic Creutzfeldt-Jakob disease.
Kovacs GG, Sanchez-Juan P, Ströbel T, Schuur M, Poleggi A, Nocentini S, Giannattasio C, Belay G, Bishop M, Capellari S, Parchi P, Gelpi E, Gal A, Bakos A, Molnar MJ, Heinemann U, Zerr I, Knight RS, Mitrova E, van Duijn C, Budka H. Kovacs GG, et al. Among authors: strobel t. Alzheimer Dis Assoc Disord. 2010 Jan-Mar;24(1):104-7. doi: 10.1097/WAD.0b013e3181ad378c. Alzheimer Dis Assoc Disord. 2010. PMID: 19571726
Genetic Creutzfeldt-Jakob disease associated with the E200K mutation: characterization of a complex proteinopathy.
Kovacs GG, Seguin J, Quadrio I, Höftberger R, Kapás I, Streichenberger N, Biacabe AG, Meyronet D, Sciot R, Vandenberghe R, Majtenyi K, László L, Ströbel T, Budka H, Perret-Liaudet A. Kovacs GG, et al. Among authors: strobel t. Acta Neuropathol. 2011 Jan;121(1):39-57. doi: 10.1007/s00401-010-0713-y. Epub 2010 Jul 1. Acta Neuropathol. 2011. PMID: 20593190
156 results