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Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 3
2024
Dörner, Marc 
ORCID: https://orcid.org/0000-0003-3229-1677; Seebach, Katharina; Heneka, Michael T.; Menze, Inga; Känel, Roland von ORCID: https://orcid.org/0000-0002-8929-5129; Euler, Sebastian; Schreiber, Frank ORCID: https://orcid.org/0000-0002-9484-8613; Arndt, Philipp; Neumann, Katja; Hildebrand, Annkatrin; John, Anna-Charlotte; Tyndall, Anthony; Kirchebner, Johannes; Tacik, Pawel; Jansen, Robin; Grimm, Alexander; Henneicke, Solveig ORCID: https://orcid.org/0000-0002-9103-7276; Perosa, Valentina ORCID: https://orcid.org/0000-0002-3551-5237; Meuth, Sven G. ORCID: https://orcid.org/0000-0003-2571-3501; Peters, Oliver; Hellmann-Regen, Julian; Preis, Lukas; Priller, Josef; Spruth, Eike Jakob; Schneider, Anja; Fliessbach, Klaus; Wiltfang, Jens; Jessen, Frank; Rostamzadeh, Ayda; Glanz, Wenzel ORCID: https://orcid.org/0000-0002-5865-4176; Schulze, Jan Ben; Schiebler, Sarah Lavinia Florence ORCID: https://orcid.org/0009-0000-8112-546X; Buerger, Katharina; Janowitz, Daniel; Perneczky, Robert; Rauchmann, Boris-Stephan ORCID: https://orcid.org/0000-0003-4547-6240; Teipel, Stefan; Kilimann, Ingo; Laske, Christoph; Munk, Matthias H.; Spottke, Annika; Roy-Kluth, Nina; Wagner, Michael ORCID: https://orcid.org/0000-0003-2589-6440; Frommann, Ingo ORCID: https://orcid.org/0000-0002-7244-2014; Lüsebrink, Falk; Dechent, Peter; Hetzer, Stefan; Scheffler, Klaus; Kleineidam, Luca; Stark, Melina; Schmid, Matthias; Ersözlü, Ersin ORCID: https://orcid.org/0000-0001-6503-5894; Brosseron, Frederic; Ewers, Michael; Schott, Björn H. ORCID: https://orcid.org/0000-0002-8237-4481; Düzel, Emrah; Ziegler, Gabriel; Mattern, Hendrik; Schreiber, Stefanie ORCID: https://orcid.org/0000-0003-4439-4374 und Bernal, Jose ORCID: https://orcid.org/0000-0003-3167-5134
(2024):
Inferior Frontal Sulcal Hyperintensities on Brain MRI Are Associated with Amyloid Positivity beyond Age—Results from the Multicentre Observational DELCODE Study.
In: Diagnostics, Bd. 14, Nr. 9, 940
[PDF, 573kB]
ORCID: https://orcid.org/0000-0003-3229-1677; Seebach, Katharina; Heneka, Michael T.; Menze, Inga; Känel, Roland von ORCID: https://orcid.org/0000-0002-8929-5129; Euler, Sebastian; Schreiber, Frank ORCID: https://orcid.org/0000-0002-9484-8613; Arndt, Philipp; Neumann, Katja; Hildebrand, Annkatrin; John, Anna-Charlotte; Tyndall, Anthony; Kirchebner, Johannes; Tacik, Pawel; Jansen, Robin; Grimm, Alexander; Henneicke, Solveig ORCID: https://orcid.org/0000-0002-9103-7276; Perosa, Valentina ORCID: https://orcid.org/0000-0002-3551-5237; Meuth, Sven G. ORCID: https://orcid.org/0000-0003-2571-3501; Peters, Oliver; Hellmann-Regen, Julian; Preis, Lukas; Priller, Josef; Spruth, Eike Jakob; Schneider, Anja; Fliessbach, Klaus; Wiltfang, Jens; Jessen, Frank; Rostamzadeh, Ayda; Glanz, Wenzel ORCID: https://orcid.org/0000-0002-5865-4176; Schulze, Jan Ben; Schiebler, Sarah Lavinia Florence ORCID: https://orcid.org/0009-0000-8112-546X; Buerger, Katharina; Janowitz, Daniel; Perneczky, Robert; Rauchmann, Boris-Stephan ORCID: https://orcid.org/0000-0003-4547-6240; Teipel, Stefan; Kilimann, Ingo; Laske, Christoph; Munk, Matthias H.; Spottke, Annika; Roy-Kluth, Nina; Wagner, Michael ORCID: https://orcid.org/0000-0003-2589-6440; Frommann, Ingo ORCID: https://orcid.org/0000-0002-7244-2014; Lüsebrink, Falk; Dechent, Peter; Hetzer, Stefan; Scheffler, Klaus; Kleineidam, Luca; Stark, Melina; Schmid, Matthias; Ersözlü, Ersin ORCID: https://orcid.org/0000-0001-6503-5894; Brosseron, Frederic; Ewers, Michael; Schott, Björn H. ORCID: https://orcid.org/0000-0002-8237-4481; Düzel, Emrah; Ziegler, Gabriel; Mattern, Hendrik; Schreiber, Stefanie ORCID: https://orcid.org/0000-0003-4439-4374 und Bernal, Jose ORCID: https://orcid.org/0000-0003-3167-5134
(2024):
Inferior Frontal Sulcal Hyperintensities on Brain MRI Are Associated with Amyloid Positivity beyond Age—Results from the Multicentre Observational DELCODE Study.
In: Diagnostics, Bd. 14, Nr. 9, 940
[PDF, 573kB]
2022
Strippel, Christine; Herrera-Rivero, Marisol; Wendorff, Mareike; Tietz, Anja K.; Degenhardt, Frauke; Witten, Anika; Schroeter, Christina; Nelke, Christopher; Golombeck, Kristin S.; Madlener, Marie; Rueber, Theodor; Ernst, Leon; Racz, Attila; Baumgartner, Tobias; Widman, Guido; Doppler, Kathrin; Thaler, Franziska; Siebenbrodt, Kai; Dik, Andre; Kerin, Constanze; Räuber, Saskia; Gallus, Marco; Kovac, Stjepana; Grauer, Oliver M.; Grimm, Alexander; Pruess, Harald; Wickel, Jonathan; Geis, Christian; Lewerenz, Jan; Goebels, Norbert; Ringelstein, Marius; Menge, Til; Tackenberg, Bjoern; Kellinghaus, Christoph; Bien, Christian G.; Kraft, Andrea; Zettl, Uwe; Ismail, Fatme Seval; Ayzenberg, Ilya; Urbanek, Christian; Sühs, Kurt-Wolfram; Tauber, Simone C.; Mues, Sigrid; Körtvelyessy, Peter; Markewitz, Robert; Paliantonis, Asterios; Elger, Christian E.; Surges, Rainer; Sommer, Claudia; Kümpfel, Tania; Gross, Catharina C.; Lerche, Holger; Wellmer, Jörg; Quesada, Carlos M.; Bergh, Florian Then; Wandinger, Klaus-Peter; Becker, Albert J.; Kunz, Wolfram S.; Meyer zu Hoerste, Gerd; Malter, Michael P.; Rosenow, Felix; Wiendl, Heinz; Kuhlenbäumer, Gregor; Leypoldt, Frank; Lieb, Wolfgang; Franke, Andre; Meuth, Sven G.; Stoll, Monika und Melzer, Nico
(2022):
A genome-wide association study in autoimmune neurological syndromes with anti-GAD65 autoantibodies.
In: Brain, Bd. 146, Nr. 3: S. 977-990
2017
Dohrn, Maike F.; Glöckle, Nicola; Mulahasanovic, Lejla; Heller, Corina; Mohr, Julia; Bauer, Christine; Riesch, Erik; Becker, Andrea; Battke, Florian; Hörtnagel, Konstanze; Hornemann, Thorsten; Suriyanarayanan, Saranya; Blankenburg, Markus; Schulz, Jörg B.; Claeys, Kristl G.; Gess, Burkhard; Katona, Istvan; Ferbert, Andreas; Vittore, Debora; Grimm, Alexander; Wolking, Stefan; Schöls, Ludger; Lerche, Holger; Korenke, G. Christoph; Fischer, Dirk; Schrank, Bertold; Kotzaeridou, Urania; Kurlemann, Gerhard; Dräger, Bianca; Schirmacher, Anja; Young, Peter; Schlotter-Weigel, Beate und Biskup, Saskia
(2017):
Frequent genes in rare diseases: panel-based next generation sequencing to disclose causal mutations in hereditary neuropathies.
In: Journal of Neurochemistry, Bd. 143, Nr. 5: S. 507-522