34 results on '"Lerche, Holger"'
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2. Correction to: Cenobamate: real-world data from a retrospective multicenter study
3. Präzisionsmedizin in der Epileptologie – wie weit sind wir wirklich?
4. Targeted gene sequencing in 6994 individuals with neurodevelopmental disorder with epilepsy
5. Tetraparesis and sensorimotor axonal polyneuropathy due to co-occurrence of Pompe disease and hereditary ATTR amyloidosis
6. Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy
7. Epileptogenese und Konsequenzen für die Therapie
8. Strength and muscle structure preserved during long-term therapy in a patient with hypokalemic periodic paralysis (Cav1.1-R1239G)
9. Neuro-Sweet syndrome - a rare differential diagnosis in aseptic meningoencephalitis
10. Drug-resistant epilepsy — time to target mechanisms
11. Besondere Bildgebung bei sonstigen genetisch determinierten Epilepsien
12. In vitro neuronal network activity as a new functional diagnostic system to detect effects of Cerebrospinal fluid from autoimmune encephalitis patients
13. Thalamic transitory ischemic attacks presenting as Jacksonian sensory march
14. Personalisierte Diagnostik und Therapie in der Neurologie: Chance und Herausforderung
15. Impact of Genetic Polymorphisms of ABCB1 (MDR1, P-Glycoprotein) on Drug Disposition and Potential Clinical Implications: Update of the Literature
16. Restless legs syndrome in psoriasis: an unexpected comorbidity
17. Differences Between MEG and High-Density EEG Source Localizations Using a Distributed Source Model in Comparison to fMRI
18. Obituary for Prof. Dr. Dr. h.c. Dipl. Ing. Frank Lehmann-Horn
19. Focal epilepsy in Glucose transporter type 1 (Glut1) defects: case reports and a review of literature
20. Genetic Biomarkers in Epilepsy
21. Regulation of ClC-2 gating by intracellular ATP
22. Potassium channels: a review of broadening therapeutic possibilities for neurological diseases
23. A conserved threonine in the S1–S2 loop of KV7.2 and KV7.3 channels regulates voltage-dependent activation
24. PRRT2-related disorders: further PKD and ICCA cases and review of the literature
25. KV7 channelopathies
26. Genetics of paroxysmal dyskinesias
27. Benigne familiäre Anfälle des Neugeborenen- und Säuglingsalters
28. Letter to the editor: confirming neonatal seizure and late onset ataxia in SCN2A Ala263Val
29. Genetische Untersuchungen bei Epilepsien – vom Labor in die Praxis
30. Estimating rate constants from single ion channel currents when the initial distribution is known
31. Skeletal muscle channelopathies
32. On identification of Na+ channel gating schemes using moving-average filtered hidden Markov models
33. Teaching course: ion channelopathies in neurology
34. Painful seizures associated with a lesion in the midcingulate cortex
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