Holger Lerche
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| Quinn S, Zhang N, Fenton TA, et al. (2024) Complex biophysical changes and reduced neuronal firing in an SCN8A variant associated with developmental delay and epilepsy. Biochimica Et Biophysica Acta. Molecular Basis of Disease. 1870: 167127 |
| Koko M, Elseed MA, Mohammed IN, et al. (2024) Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy. European Journal of Human Genetics : Ejhg |
| Kegele J, Wagner T, Kowenski T, et al. (2024) Long-term clinical course and treatment outcomes of individuals with Nodding Syndrome. Journal of the Neurological Sciences. 457: 122893 |
| Lyu H, Boßelmann CM, Johannesen KM, et al. (2023) Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia. Ebiomedicine. 98: 104855 |
| Lauerer RJ, Lerche H. (2023) Voltage-gated calcium channels in genetic epilepsies. Journal of Neurochemistry |
| Boothman I, Clayton LM, McCormack M, et al. (2023) Testing for pharmacogenomic predictors of ppRNFL thinning in individuals exposed to vigabatrin. Frontiers in Neuroscience. 17: 1156362 |
| Kreilkamp BAK, Stier C, Rauf EH, et al. (2023) Multi-spectral diffusion MRI mega-analysis in genetic generalized epilepsy: Relation to outcomes. Neuroimage. Clinical. 39: 103474 |
| Knierim E, Vogt J, Kintscher M, et al. (2023) Mutations in plasticity-related-gene-1 (PRG-1) protein contribute to hippocampal seizure susceptibility and modify epileptic phenotype. Cerebral Cortex (New York, N.Y. : 1991) |
| Müller P, Takacs DS, Hedrich UBS, et al. (2023) KCNA1 gain-of-function epileptic encephalopathy treated with 4-aminopyridine. Annals of Clinical and Translational Neurology |
| Müller P, Lerche H. (2023) [Gene Therapy for Epilepsy: Clinical Studies are on the Road]. Fortschritte Der Neurologie-Psychiatrie |