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Fortschritte Der Neurologie-Psychiatrie|February 23, 2023
[Gene Therapies in Motor Neuron Diseases ALS and SMA]René GüntherAmyotrophic Lateral Sclerosis & Frontotemporal Degeneration|April 12, 2025
SOD1-ALS mimicking an inflammatory neuropathy: a case reportHanna Sophie Lapp, René GüntherFortschritte Der Neurologie-Psychiatrie|November 6, 2023
[Psychologically guided group meetings for family caregivers of ALS patients]Elisa Aust, René Günther, Andreas Hermann, et al.Muscle & Nerve|July 19, 2023
Impaired diaphragmatic motility in treatment-naive adult patients with spinal muscular atrophy improved during nusinersen treatmentMaren Freigang, Simona Langner, Andreas Hermann, et al.Journal of Clinical Medicine|January 11, 2022
Caregivers' View of Socio-Medical Care in the Terminal Phase of Amyotrophic Lateral Sclerosis-How Can We Improve Holistic Care in ALS?Katharina Linse, Elisa Aust, René Günther, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|March 3, 2021
The palmomental reflex in amyotrophic lateral sclerosis - a clinical sign of executive or motor dysfunction?Maximilian Vidovic, Elisa Aust, Andreas Hermann, et al.International Journal of Molecular Sciences|May 24, 2020
Human Spinal Motor Neurons Are Particularly Vulnerable to Cerebrospinal Fluid of Amyotrophic Lateral Sclerosis PatientsStefan Bräuer, René Günther, Jared Sterneckert, et al.Journal of Clinical Pharmacology|May 1, 2019
Off-Label Treatment of 4 Amyotrophic Lateral Sclerosis Patients With 4-AminopyridineKevin Peikert, Marcel Naumann, René Günther, et al.Neurological Research and Practice|February 21, 2024
Macrophage inclusions in cerebrospinal fluid following treatment initiation with antisense oligonucleotide therapies in motor neuron diseasesMaximilian Vidovic, Mario Menschikowski, Maren Freigang, et al.Brain & Development|February 8, 2024
'Reading the palm' - A pilot study of grip and finger flexion strength as an outcome measure in 5q spinal muscular atrophyConstanze Weber, Anne Müller, Maren Freigang, et al.Pageof 10