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Zeitschriftenartikel
Tzeplaeff, Laura 
ORCID: https://orcid.org/0009-0003-7643-3232; Galhoz, Ana; Meijs, Clara; Caldi Gomes, Lucas; Kovac, Andrej; Menzel, Amrei; Değirmenci, Hatice; Alaamel, Abir; Kaya, Hüseyin Can; Çelik, Ali Günalp; Dinçer, Sine; Korucuk, Meltem; Karaüzüm, Sibel Berker; Bayraktar, Elif; Çiftçi, Vildan; Bilge, Uğur; Koç, Filiz; Demleitner, Antonia F.; Buchberger, Anne; Heynitz, Ricarda von; Gmeiner, Vincent; Knellwolf, Christina; Mouzouri, Mohammed; Wuu, Joanne; Başak, A. Nazli; Andersen, Peter Munch; Kohlmayer, Florian; Ashton, Nicholas J.; Kuban, Wojciech; Lenz, Christof; Rogers, Mary-Louise; Zilka, Norbert; Corcia, Philippe; Lerner, Yossef; Weber, Markus; Turcanova Koprusakova, Monika; Uysal, Hilmi; Benatar, Michael; Menden, Michael P. und Lingor, Paul ORCID: https://orcid.org/0000-0001-9362-7096
(2025):
Identification of a presymptomatic and early disease signature for amyotrophic lateral sclerosis (ALS): protocol of the premodiALS study.
In: Neurological Research and Practice, Bd. 7, 56
[PDF, 1MB]
ORCID: https://orcid.org/0009-0003-7643-3232; Galhoz, Ana; Meijs, Clara; Caldi Gomes, Lucas; Kovac, Andrej; Menzel, Amrei; Değirmenci, Hatice; Alaamel, Abir; Kaya, Hüseyin Can; Çelik, Ali Günalp; Dinçer, Sine; Korucuk, Meltem; Karaüzüm, Sibel Berker; Bayraktar, Elif; Çiftçi, Vildan; Bilge, Uğur; Koç, Filiz; Demleitner, Antonia F.; Buchberger, Anne; Heynitz, Ricarda von; Gmeiner, Vincent; Knellwolf, Christina; Mouzouri, Mohammed; Wuu, Joanne; Başak, A. Nazli; Andersen, Peter Munch; Kohlmayer, Florian; Ashton, Nicholas J.; Kuban, Wojciech; Lenz, Christof; Rogers, Mary-Louise; Zilka, Norbert; Corcia, Philippe; Lerner, Yossef; Weber, Markus; Turcanova Koprusakova, Monika; Uysal, Hilmi; Benatar, Michael; Menden, Michael P. und Lingor, Paul ORCID: https://orcid.org/0000-0001-9362-7096
(2025):
Identification of a presymptomatic and early disease signature for amyotrophic lateral sclerosis (ALS): protocol of the premodiALS study.
In: Neurological Research and Practice, Bd. 7, 56
[PDF, 1MB]
Vondel, Liedewei van de; De Winter, Jonathan; Beijer, Danique; Coarelli, Giulia; Wayand, Melanie; Palvadeau, Robin; Pauly, Martje G.; Klein, Katrin; Rautenberg, Maren; Guillot-Noel, Lena; Deconinck, Tine; Vural, Atay; Ertan, Sibel; Dogu, Okan; Uysal, Hilmi; Brankovic, Vesna; Herzog, Rebecca; Brice, Alexis; Durr, Alexandra; Klebe, Stephan; Stock, Friedrich; Bischoff, Almut Turid; Rattay, Tim W.; Sobrido, Maria-Jesus; De Michele, Giovanna; De Jonghe, Peter; Klopstock, Thomas; Lohmann, Katja; Zanni, Ginevra; Santorelli, Filippo M.; Timmerman, Vincent; Haack, Tobias B.; Zuchner, Stephan; Schuele, Rebecca; Stevanin, Giovanni; Synofzik, Matthis; Basak, A. Nazli und Baets, Jonathan
(2022):
De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia.
In: Movement Disorders, Bd. 37, Nr. 6: S. 1175-1186
[PDF, 1MB]