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The Journal of Cell Biology|November 25, 2015
TDP-43 is intercellularly transmitted across axon terminalsMarisa S Feiler, Benjamin Strobel, Axel Freischmidt, et al.Experimental Neurology|October 10, 2020
Hemizygous deletion of Tbk1 worsens neuromuscular junction pathology in TDP-43G298S transgenic miceKirsten Sieverding, Johannes Ulmer, Clara Bruno, et al.Neurobiology of Aging|May 10, 2022
Methylome analysis of ALS patients and presymptomatic mutation carriers in blood cellsWolfgang P Ruf, Eilis Hannon, Axel Freischmidt, et al.Neurobiology of Aging|July 5, 2015
Serum microRNAs in sporadic amyotrophic lateral sclerosisAxel Freischmidt, Kathrin Müller, Lisa Zondler, et al.Journal of Neurology, Neurosurgery, and Psychiatry|September 14, 2021
De novo mutations in SOD1 are a cause of ALSKathrin Müller, Ki-Wook Oh, Angelica Nordin, et al.Cells|April 30, 2021
Protein Binding Partners of Dysregulated miRNAs in Parkinson's Disease SerumWolfgang P Ruf, Axel Freischmidt, Veselin Grozdanov, et al.Acta Neuropathologica|November 19, 2015
Age-dependent defects of alpha-synuclein oligomer uptake in microglia and monocytesCorinna Bliederhaeuser, Veselin Grozdanov, Anna Speidel, et al.Cellular and Molecular Life Sciences : CMLS|July 22, 2018
Dysregulation of a novel miR-1825/TBCB/TUBA4A pathway in sporadic and familial ALSAnika M Helferich, Sarah J Brockmann, Jörg Reinders, et al.Brain : a Journal of Neurology|December 11, 2025
Somatic gene mutations in the motor cortex of patients with sporadic amyotrophic lateral sclerosisÓscar González-Velasco, Rosanna Parlato, Rüstem Yilmaz, et al.Brain : a Journal of Neurology|September 7, 2014
Serum microRNAs in patients with genetic amyotrophic lateral sclerosis and pre-manifest mutation carriersAxel Freischmidt, Kathrin Müller, Lisa Zondler, et al.Pageof 5