J. Ernst

发表

Lennox-Gastaut syndrome: a consensus approach on diagnosis, assessment, management, and trial methodology

J. Cross, W. Blume, J. Wheless, 2009, Lancet Neurology.

Effects of Levetiracetam and Sulthiame on EEG in benign epilepsy with centrotemporal spikes: A randomized controlled trial

M. Mandl, U. Stephani, W. Koch, 2018, Seizure.

Benign Partial Epilepsy—Treatment with Sulthiame

I. Tuxhorn, H. Doose, W. Baier, 1988, Developmental medicine and child neurology.

A human keratin 14 "knockout": the absence of K14 leads to severe epidermolysis bullosa simplex and a function for an intermediate filament protein.

E. Fuchs, Qian-chun Yu, B. Zabel, 1994, Genes & development.

Erratum: Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy (Epilepsia (2013) 54 (256-264) DOI:10.1111/epi.12517)

H. Mefford, C. Elger, A. Scabar, 2013 .

Two novel CLCN2 mutations accelerating chloride channel deactivation are associated with idiopathic generalized epilepsy

H. Lerche, G. Teodorescu, J. Poncer, 2009, Human Mutation.

Pharmacology, Efficacy, and Tolerability of Potassium Bromide in Childhood Epilepsy

Peter Burkart, J. Ernst, R. Korinthenberg, 2007, Journal of child neurology.

Bromides were effective in intractable epilepsy with generalized tonic-clonic seizures and onset in early childhood

H. Doose, W. Baier, J. Ernst, 1988, Brain and Development.

Effectiveness and tolerability of rufinamide in children and adults with refractory epilepsy: First European experience

T. Bast, R. Boor, G. Kurlemann, 2009, Epilepsy & Behavior.

Exon‐disrupting deletions of NRXN1 in idiopathic generalized epilepsy

H. Mefford, H. Wichmann, U. Stephani, 2013, Epilepsia.

First European long-term experience with the orphan drug rufinamide in childhood-onset refractory epilepsy

T. Bast, R. Boor, G. Kurlemann, 2010, Epilepsy & Behavior.

Foix‐Chavany‐Marie (anterior operculum) syndrome in childhood: a reappraisal of Worster‐Drought syndrome

E Kruse, F. Hanefeld, H. Christen, 2000, Developmental medicine and child neurology.

Two novel CLCN2 mutations accelerating chloride channel deactivation are associated with idiopathic generalized epilepsy

H. Lerche, G. Teodorescu, J. Poncer, 2009, Human mutation.

Late-Onset Globoid Cell Leukodystrophy: Unusual Ultrastructural Pathology and Subtotal β-Galactocerebrosidase Deficiency

J. Bohl, H. Goebel, J. Ernst, 1990, Journal of child neurology.

Atypical case of Aicardi-Goutières syndrome with late-onset myoclonic status.

D. Rating, P. Lebon, G. Hoffmann, 2007, Epileptic disorders : international epilepsy journal with videotape.