Department of Molecular Neurology


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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

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To

Abstract

Journal

Characterization of gait variability in multiple system atrophy and Parkinson's disease (2020) Sidoroff V, Raccagni C, Kaindlstorfer C, Eschlboeck S, Fanciulli A, Granata R, Eskofier B, et al. Journal article The Joint-Brain Axis: Insights From Rheumatoid Arthritis on the Crosstalk Between Chronic Peripheral Inflammation and the Brain (2020) Süß P, Rothe T, Hoffmann A, Schlachetzki JCM, Winkler J Journal article, Review article Toxic Metamorphosis-How Changes from Lysosomal to Cytosolic pH Modify the Alpha-Synuclein Aggregation Pattern (2020) Eymsh B, Drobny A, Heyn TR, Xiang W, Lucius R, Schwarz K, Keppler JK, et al. Journal article Inertial sensor-based gait parameters reflect patient-reported fatigue in multiple sclerosis (2020) Ibrahim A, Küderle A, Gaßner H, Klucken J, Eskofier B, Kluge F Journal article Unique signatures of stress-induced senescent human astrocytes (2020) Simmnacher K, Krach F, Schneider Y, Alecu JE, Mautner L, Klein P, Roybon L, et al. Journal article Compensatory neuritogenesis of serotonergic afferents within the striatum of a transgenic rat model of Parkinson's disease (2020) Stemick J, Gauer C, Wihan J, Moceri S, Xiang W, von Hörsten S, Kohl Z, Winkler J Journal article Author Correction: A monocyte gene expression signature in the early clinical course of Parkinson’s disease (Scientific Reports, (2018), 8, 1, (10757), 10.1038/s41598-018-28986-7) (2020) Schlachetzki J, Prots I, Tao J, Chun HB, Saijo K, Gosselin D, Winner B, et al. Journal article, Erratum Intracellular A53T Mutant alpha-Synuclein Impairs Adult Hippocampal Newborn Neuron Integration (2020) Winner B, Regensburger M, Stemick J, Masliah E, Kohl Z Journal article, other Intracellular A53T Mutant α-Synuclein Impairs Adult Hippocampal Newborn Neuron Integration (2020) Regensburger M, Stemick J, Masliah E, Kohl Z, Winner B Journal article New CaV1.2 channelopathy with high-functioning autism, affective disorder, severe dental enamel defects, a short QT interval, and a novel cacna1c loss-of-function mutation (2020) Endres D, Decher N, Röhr I, Vowinkel K, Domschke K, Komlosi K, Tzschach A, et al. Journal article