54 results on '"Lerche, Holger"'
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2. Klinisches Ansprechen mit ML vorhersagen
3. Präzisionsmedizin in der Epileptologie – wie weit sind wir wirklich?
4. Tetraparesis and sensorimotor axonal polyneuropathy due to co-occurrence of Pompe disease and hereditary ATTR amyloidosis
5. Drug-resistant epilepsy — time to target mechanisms
6. In allen Altersgruppen gleich gutes Ansprechen
7. Verbesserte Patientenselektion für Epilepsie-OP
8. Neuro-Sweet syndrome - a rare differential diagnosis in aseptic meningoencephalitis
9. Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish
10. Personalisierte Diagnostik und Therapie in der Neurologie
11. Epileptogenese und Konsequenzen für die Therapie
12. Obituary for Prof. Dr. Dr. h.c. Dipl. Ing. Frank Lehmann-Horn
13. In vitro neuronal network activity as a new functional diagnostic system to detect effects of Cerebrospinal fluid from autoimmune encephalitis patients
14. Strength and muscle structure preserved during long-term therapy in a patient with hypokalemic periodic paralysis (Cav1.1-R1239G)
15. Increased Functional MEG Connectivity as a Hallmark of MRI-Negative Focal and Generalized Epilepsy
16. Nerve Ultrasound Predicts Treatment Response in Chronic Inflammatory Demyelinating Polyradiculoneuropathy—a Prospective Follow-Up
17. Epilepsiechirurgie hochwirksam bei Kindern
18. Besondere Bildgebung bei sonstigen genetisch determinierten Epilepsien
19. Human Cerebrospinal fluid promotes long-term neuronal viability and network function in human neocortical organotypic brain slice cultures
20. Thalamic transitory ischemic attacks presenting as Jacksonian sensory march
21. Neue Therapieoption für Kataplexie bei Narkolepsie
22. SRF modulates seizure occurrence, activity induced gene transcription and hippocampal circuit reorganization in the mouse pilocarpine epilepsy model
23. Everolimus als neue personalisierte Therapie – Evidenz aus der EXIT-3-Studie
24. Letter to the editor: confirming neonatal seizure and late onset ataxia in SCN2A Ala263Val
25. Keine Vorteile durch zusätzliches Levetiracetam
26. Genetische Untersuchungen bei Epilepsien – vom Labor in die Praxis
27. Langzeitbehandlung mit responsiver Hirnstimulation
28. Impact of Genetic Polymorphisms of ABCB1 (MDR1, P-Glycoprotein) on Drug Disposition and Potential Clinical Implications: Update of the Literature
29. A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy
30. Differences Between MEG and High-Density EEG Source Localizations Using a Distributed Source Model in Comparison to fMRI
31. Häufige Epilepsieformen im Kindes- und Erwachsenenalter
32. Focal epilepsy in Glucose transporter type 1 (Glut1) defects: case reports and a review of literature
33. Hochdosis Midazolam erweist sich als sicher
34. Genetic Biomarkers in Epilepsy
35. Encephalopathic Susac’s Syndrome associated with livedo racemosa in a young woman before the completion of family planning
36. Episodic itch in a case of spinal glioma
37. Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes
38. Regulation of ClC-2 gating by intracellular ATP
39. PRRT2-related disorders: further PKD and ICCA cases and review of the literature
40. A conserved threonine in the S1–S2 loop of KV7.2 and KV7.3 channels regulates voltage-dependent activation
41. Potassium channels: a review of broadening therapeutic possibilities for neurological diseases
42. KV7 channelopathies
43. Praktische Epilepsietherapie
44. Retraction Note: Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies
45. CLCN2 variants in idiopathic generalized epilepsy
46. Genetics of paroxysmal dyskinesias
47. Painful seizures associated with a lesion in the midcingulate cortex
48. 15q13.3 microdeletions increase risk of idiopathic generalized epilepsy
49. Benigne familiäre Anfälle des Neugeborenen- und Säuglingsalters
50. Estimating rate constants from single ion channel currents when the initial distribution is known
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