Prof. Dr. Jürgen Winkler

Professur für Molekulare Neurologie

A sensorimotor enhanced neuromusculoskeletal model for simulating postural control of upright standing (2024) Shanbhag J, Fleischmann S, Wechsler I, Gaßner H, Winkler J, Eskofier B, Koelewijn A, et al. Journal article CSF1R-mediated myeloid cell depletion shifts the ratio of motor cortical excitatory to inhibitory neurons in a multiple system atrophy model (2024) Gauer C, Battis K, Schneider Y, Florio JB, Mante M, Kim HY, Rissman RA, et al. Journal article Young human alpha synuclein transgenic (BAC-SNCA) mice display sex- and gene-dose-dependent phenotypic disturbances (2024) Moceri S, Bäuerle N, Habermeyer J, Ratz-Wirsching V, Harrer J, Distler J, Schulze-Krebs A, et al. Journal article Modelling postural control of upright standing during translational perturbations (2024) Shanbhag J, Fleischmann S, Gaßner H, Winkler J, Eskofier B, Koelewijn A, Wartzack S, Miehling J Conference contribution, Abstract of a poster Mobile digital gait analysis captures effects of botulinum toxin in hereditary spastic paraplegia (2024) Ibrahim A, Ollenschläger M, Klebe S, Schüle R, Jeschonneck N, Kellner M, Loris E, et al. Journal article Plasma Neurofilaments: Potential Biomarkers of SPG11-Related Hereditary Spastic Paraplegia (2024) Krumm L, Winkler J, Winner B, Regensburger M Journal article Sex-specific pleiotropic changes in emotional behavior and alcohol consumption in human α-synuclein A53T transgenic mice during early adulthood (2024) Kalinichenko L, Kohl Z, Mühle C, Hassan Z, Hahn A, Schmitt EM, Macht K, et al. Journal article Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patients. (2024) Krumm L, Pozner T, Zagha N, Coras R, Arnold P, Tsaktanis T, Scherpelz K, et al. Journal article Patient perspectives on the use of digital medical devices and health data for AI-driven personalised medicine in Parkinson’s Disease (2024) Paccoud I, Valero MM, Marín LC, Bontridder N, Ibrahim A, Winkler J, Fomo M, et al. Journal article Novel Homozygous FA2H Variant Causing the Full Spectrum of Fatty Acid Hydroxylase-Associated Neurodegeneration (SPG35) (2023) German A, Jukic J, Laner A, Arnold P, Socher E, Mennecke A, Schmidt M, et al. Journal article