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Anzahl der Publikationen: 3
Zeitschriftenartikel
Caldi Gomes, Lucas; Galhoz, Ana; Jain, Gaurav; Roser, Anna-Elisa; Maass, Fabian; Carboni, Eleonora; Barski, Elisabeth; Lenz, Christof; Lohmann, Katja; Klein, Christine; Baehr, Mathias; Fischer, Andre; Menden, Michael P. und Lingor, Paul
(2022):
Multi-omic landscaping of human midbrains identifies disease-relevant molecular targets and pathways in advanced-stage Parkinson's disease.
In: Clinical and Translational Medicine, Bd. 12, Nr. 1, e692
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
Hopfner, Franziska; Müller, Stefanie H.; Szymczak, Silke; Junge, Olaf; Tittmann, Lukas; May, Sandra; Lohmann, Katja; Grallert, Harald; Lieb, Wolfgang; Strauch, Konstantin und Müller-Nurasyid, Martina
(2020):
Rare Variants in Specific Lysosomal Genes Are Associated With Parkinson's Disease.
In: Movement disorders : official journal of the Movement Disorder Society, Bd. 35, Nr. 7: S. 1245-1248