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Eye movement alterations in presymptomatic C9orf72 expansion gene carriers

2021 . Behler, Anna | Knehr, Antje | Finsel, Julia | Kunz, Martin S. | Lang, Christina | Müller, Kathrin | Müller, Hans-Peter | Pinkhardt, Elmar H. | Ludolph, Albert C. | Lulé, Dorothée | Kassubek, Jan

FUS mutations dominate TBK1 mutations in FUS/TBK1 double-mutant ALS/FTD pedigrees

2021 . Brenner, David | Müller, Kathrin | Lattante, Serena | Yilmaz, Rüstem | Knehr, Antje | Freischmidt, Axel | Ludolph, Albert C. | Andersen, Peter M. | Weishaupt, Jochen H.

SPG7 mutations in amyotrophic lateral sclerosis: a genetic link to hereditary spastic paraplegia

2020 . Osmanovic, Alma | Widjaja, Maylin | Förster, Alisa | Weder, Julia | Wattjes, Mike P. | Lange, Inken | Sarikidi, Anastasia | Auber, Bernd | Raab, Peter | Christians, Anne | Preller, Matthias | Petri, Susanne | Weber, Ruthild G.

Congenic expression of poly-GA but not poly-PR in mice triggers selective neuron loss and interferon responses found in C9orf72 ALS