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Number of items: 3.

2021

Tietz, Anja K., Angstwurm, Klemens, Baumgartner, Tobias, Doppler, Kathrin ORCID: 0000-0003-2883-0009, Eisenhut, Katharina ORCID: 0000-0001-6448-3126, Elisak, Martin, Franke, Andre ORCID: 0000-0003-1530-5811, Golombeck, Kristin S., Handreka, Robert, Kaufmann, Max ORCID: 0000-0002-1954-4425, Kraemer, Markus, Kraft, Andrea, Lewerenz, Jan, Lieb, Wolfgang, Madlener, Marie, Melzer, Nico, Mojzisova, Hana, Moeller, Peter, Pfefferkorn, Thomas, Pruess, Harald, Rostasy, Kevin, Schnegelsberg, Margret, Schroeder, Ina, Siebenbrodt, Kai, Suehs, Kurt-Wolfram, Wickel, Jonathan, Wandinger, Klaus-Peter, Leypoldt, Frank ORCID: 0000-0002-8972-515X and Kuhlenbaeumer, Gregor (2021). Genome-wide Association Study Identifies 2 New Loci Associated With Anti-NMDAR Encephalitis. Neurol.-Neuroimmunol. Neuroinflammation, 8 (6). PHILADELPHIA: LIPPINCOTT WILLIAMS & WILKINS. ISSN 2332-7812

2019

Hopfner, Franziska ORCID: 0000-0001-6524-0281, Mueller, Stefanie H., Steppat, Dagmar, Miller, Joanna, Schmidt, Nele, Wandinger, Klaus-Peter, Leypoldt, Frank, Berg, Daniela, Franke, Andre, Lieb, Wolfgang, Tittmann, Lukas, Balzer-Geldsetzer, Monika, Baudrexel, Simon, Dodel, Richard, Hilker-Roggendorf, Ruediger, Kalbe, Elke, Kassubek, Jan ORCID: 0000-0002-7106-9270, Klockgether, Thomas, Liepelt-Scarfone, Inga, Mollenhauer, Brit, Neuser, Petra, Reetz, Kathrin, Riedel, Oliver, Schulte, Claudia ORCID: 0000-0003-4006-1265, Schulz, Joerg B., Spottke, Annika, Storch, Alexander, Trenkwalder, Claudia, Wittchen, Hans-Ulrich, Witt, Karsten, Wuellner, Ullrich, Deuschl, Gunther ORCID: 0000-0002-4176-9196 and Kuhlenbaeumer, Gregor (2019). No association between Parkinson disease and autoantibodies against NMDA-type glutamate receptors. Transl. Neurodegener., 8. LONDON: BMC. ISSN 2047-9158

2016

Rempe, Torge ORCID: 0000-0003-0538-1378, Kuhlenbaeumer, Gregor, Krueger, Stefanie, Biskup, Saskia, Matschke, Jakob ORCID: 0000-0001-6080-0198, Hagel, Christian, Deuschl, Guenther and van Eimeren, Thilo ORCID: 0000-0002-6951-2325 (2016). Early-onset parkinsonism due to compound heterozygous POLG mutations. Parkinsonism Relat. Disord., 29. S. 135 - 138. OXFORD: ELSEVIER SCI LTD. ISSN 1873-5126

This list was generated on Wed Apr 24 05:45:04 2024 CEST.