38 results on '"Lerche, Holger"'
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2. Long-term clinical course and treatment outcomes of individuals with Nodding Syndrome
3. Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia
4. Sponge EEG is equivalent regarding signal quality, but faster than routine EEG
5. A SCN8A variant associated with severe early onset epilepsy and developmental delay: Loss- or gain-of-function?
6. Motor cortex excitability in seizure-free STX1B mutation carriers with a history of epilepsy and febrile seizures
7. Shaping the future of European epilepsy research: Final meeting report from EPICLUSTER
8. Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsy
9. Generation of an induced pluripotent stem cell (iPSC) line from a patient with GEFS+ carrying a STX1B (p.Lys45delinsArgMetCysIleGlu and p.Leu46Met) mutation
10. Retigabine and gabapentin restore channel function and neuronal firing in a cellular model of an epilepsy-associated dominant-negative KCNQ5 variant.
11. Differential excitatory vs inhibitory SCN expression at single cell level regulates brain sodium channel function in neurodevelopmental disorders.
12. Genetic potassium channel-associated epilepsies: Clinical review of the Kv family.
13. Investigation of GRIN2A in common epilepsy phenotypes
14. Do Glut1 (glucose transporter type 1) defects exist in epilepsy patients responding to a ketogenic diet?
15. Generation of an induced pluripotent stem cell (iPSC) line (HIHDNEi003-A) from a patient with developmental and epileptic encephalopathy carrying a KCNA2 (p.Thr374Ala) mutation
16. Generation of an induced pluripotent stem cell (iPSC) line from a patient with developmental and epileptic encephalopathy carrying a KCNA2 (p.Leu328Val) mutation.
17. A multicenter survey of clinical experiences with perampanel in real life in Germany and Austria
18. Establishment of a human induced pluripotent stem cell (iPSC) line (HIHDNEi002-A) from a patient with developmental and epileptic encephalopathy carrying a KCNA2 (p.Arg297Gln) mutation
19. Nerve Ultrasound Predicts Treatment Response in Chronic Inflammatory Demyelinating Polyradiculoneuropathy-a Prospective Follow-Up.
20. Periodic EEG patterns in sporadic Creutzfeld-Jakob-Disease can be benzodiazepine-responsive and be difficult to distinguish from non-convulsive status epilepticus.
21. Cervical spinal MRI in a patient with a vagus nerve stimulator (VNS)
22. Efficacy and safety of ezogabine/retigabine as adjunctive therapy to specified single antiepileptic medications in an open-label study of adults with partial-onset seizures.
23. Genetic Biomarkers in Epilepsy.
24. Mutation in the mitochondrial tRNA(Ile) gene causes progressive myoclonus epilepsy.
25. Mutation in the mitochondrial tRNAIle gene causes progressive myoclonus epilepsy.
26. Constituents of the rhizome of Homalomena occulta
27. Optically pumped magnetometers reveal fasciculations non-invasively.
28. Homozygous mutation in TXNRD1 is associated with genetic generalized epilepsy.
29. Crototropone, a new tropone derivative from Croton zehntneri
30. Incidence and mechanisms of cardiorespiratory arrests in epilepsy monitoring units (MORTEMUS): a retrospective study.
31. Role of GRM4 in idiopathic generalized epilepsies analysed by genetic association and sequence analysis
32. Immunohistochemical analysis of KCNQ3 potassium channels in mouse brain
33. Immunohistochemical analysis of KCNQ2 potassium channels in adult and developing mouse brain
34. Constituents of the leaves of Eucalyptus saligna
35. Quantification of brain atrophy in patients with myotonic dystrophy and proximal myotonic myopathy: a controlled 3-dimensional magnetic resonance imaging study
36. Possible Effect of Corticoids on Hemiplegic Attacks in Severe Hemiplegic Migraine.
37. Triterpene saponins from Schefflera abyssinica
38. A Genome-wide Analysis of Severe Cutaneous Adverse Drug Reactions to Anti-epileptic Drugs.
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