Publikationen von Sandra Nischwitz

Gisevius, B.; Tokic, M.; Poser, P.; Fisse, A. L.; Grueter, T.; Berthele, A.; Giglhuber, K.; Flaskamp, M.; Fleischer, V.; Bittner, S. et al.; Groppa, S.; Luessi, F.; Bayas, A.; Meuth, S.; Heesen, C.; Trebst, C.; Wildemann, B.; Bergh, F. T.; Antony, G.; Kuempfel, T.; Paul, F.; Nischwitz, S.; Tumani, H.; Zettl, U. K.; Hemmer, B.; Wiendl, H.; Zipp, F.; Timmesfeld, N.; Gold, R.; Motte, J.; Salmen, A.: Disease course and disease-modifying treatment in men and women with early MS from the German NationMS cohort. In MULTIPLE SCLEROSIS JOURNAL, 29, S. 435 - 436. 9th Joint ECTRIMS-ACTRIMS meeting, Milan, ITALY, 11. Oktober 2023 - 13. Oktober 2023. (2023)

Nischwitz, S.; Knop, M.; Weber, F.; Uhr, M.; Saemann, P.: Serum interleukin 16 levels probed as predictor of longitudinal global and regional brain volume and lesion volume changes in multiple sclerosis. In MULTIPLE SCLEROSIS JOURNAL, 29, S. 892 - 893. 9th Joint ECTRIMS-ACTRIMS meeting, Milan, ITALY, 11. Oktober 2023 - 13. Oktober 2023. (2023)

Arloth, J.; Eraslan, G.; Andlauer, T.; Gieger, C.; Gold, R.; Heilmann-Heimbach, S.; Kacprowski, T.; Meitinger, T.; Laudes, M.; Luessi, F. et al.; Mueller-Myhsok, B.; Nischwitz, S.; Peters, A.; Paul, F.; Rawal, R.; Strauch, K.; Wiendl, H.; Hemmer, B.; Theis, F.; Binder, E.; Mueller, N.: Identification of functionally relevant genetic variants associated with multiple sclerosis using deep learning. In MULTIPLE SCLEROSIS JOURNAL, 25, S. 906 - 907. 35th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS) / 24th Annual Conference of Rehabilitation in MS, Stockholm, SWEDEN, 11. September 2019 - 13. September 2019. (2019)

Maccarrone, G.; Nischwitz, S.; Deininger, S. -.; Stadelmann, C.; Koenig, F. B.; Turck, C. W.; Weber, F.: Peptide identification and mapping on MS tissue by MALDI IMAGING. In MULTIPLE SCLEROSIS JOURNAL, 21 (Supplement 11), P335, S. 131 - 132. 31st Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS), Barcelona, SPAIN, 07. Oktober 2015 - 10. Oktober 2015. SAGE Publications Ltd., London EC1Y 1SP, England (2015)

Dankowski, T.; Buck, D.; Andlauer, T. F.; Antony, G.; Bayas, A.; Bechmann, L.; Berthele, A.; Bettecken, T.; Chan, A.; Franke, A. et al.; Gold, R.; Graetz, C.; Haas, J.; Hecker, M.; Herms, S.; Hohlfeld, R.; Infante-Duarte, C.; Joeckel, K. -.; Kieseier, B. C.; Knier, B.; Knop, M.; Lichtner, P.; Lieb, W.; Lill, C. M.; Limmroth, V.; Linker, R. A.; Loleit, V.; Meuth, S.; Moebus, S.; Müller-Myhsok, B.; Nischwitz, S.; Noethen, M. M.; Friedemann, P.; Pütz, B.; Ruck, T.; Salmen, A.; Stangel, M.; Stellmann, J. -.; Strauch, K.; Stuerner, K. H.; Tackenberg, B.; Bergh, F. T.; Tumani, H.; Waldenberger, M.; Weber, F.; Wiend, H.; Wildemann, B.; Zettl, U. K.; Ziemann, U.; Zipp, F.; Hemmer, B.; Ziegler, A.: Exome Array GWAS in 10,000 Germans Identifies Association between MUC22 and Multiple Sclerosis. In HUMAN HEREDITY, 79 (1), S. 32 - 33. 43rd European Mathematical Genetics Meeting (EMGM), Brest, France, 16. April 2015 - 17. April 2015. Karger, Basel, CH (2015)

Knop, M.; Kirmeier, T.; Faber, H.; Nischwitz, S.; Turck, C.; Weber, F.: Glatiramer Acetate Induced Intracellular Transgelin-2 Elevation Reduces MMP-9 Expression in Human Peripheral Blood Mononuclear Cells. In NEUROLOGY, 80 (Supplement), P05.147. 65th Annual Meeting of the American-Academy-of-Neurology (AAN), San Diego, CA, 16. März 2013 - 23. März 2013. (2013)