Stephan Lauxmann
Hoppe Seyler Str. 3
Tuebingen, BW 72076, Germany
Tuebingen, BW 72076, Germany
Last Updated: 09/26/2026
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Found 18 publications
Antineuronal antibody titres in autoimmune encephalitis: clinical implications for diagnosis and long-term immunotherapy.
Journal: Frontiers in immunology
Published: December 19, 2025
Reliable detection of focal onset impaired awareness seizures in patients with epilepsy using wearable ECG: Development and validation study.
Journal: Computer methods and programs in biomedicine
Published: May 22, 2025
Correction to: Cenobamate: real-world data from a retrospective multicenter study.
Journal: Journal of neurology
Published: August 21, 2024
Connectome-based disentangling of epilepsy networks from insular stereoelectroencephalographic leads.
Journal: Frontiers in neurology
Published: July 06, 2024
Cenobamate: real-world data from a retrospective multicenter study.
Journal: Journal of neurology
Published: April 25, 2024
Loss or gain of function? Effects of ion channel mutations on neuronal firing depend on the neuron type.
Journal: Frontiers in neurology
Published: March 27, 2023
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.
Journal: medRxiv : the preprint server for health sciences
Published: March 03, 2023
4-Aminopyridine is a promising treatment option for patients with gain-of-function KCNA2-encephalopathy.
Journal: Science translational medicine
Published: September 13, 2021
In vitro effects of eslicarbazepine (S-licarbazepine) as a potential precision therapy on SCN8A variants causing neuropsychiatric disorders.
Journal: British journal of pharmacology
Published: August 20, 2021
Therapeutic Potential of Sodium Channel Blockers as a Targeted Therapy Approach in KCNA1-Associated Episodic Ataxia and a Comprehensive Review of the Literature.
Journal: Frontiers in neurology
Published: May 01, 2021
Genetics of Paroxysmal Dyskinesia: Novel Variants Corroborate the Role of KCNA1 in Paroxysmal Dyskinesia and Highlight the Diverse Phenotypic Spectrum of KCNA1- and SLC2A1-Related Disorders.
Journal: Frontiers in neurology
Published: April 27, 2021
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications.
Journal: Brain : a journal of neurology
Published: March 12, 2021
Last Updated: 09/26/2026