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期刊名:Epileptic disorders

缩写:EPILEPTIC DISORD

ISSN:1294-9361

e-ISSN:1950-6945

IF/分区:2.7/Q2

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共收录本刊相关文章索引1195
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Katharina Moser,Dorottya Cserpan,Antonio Giulio Gennari et al. Katharina Moser et al.
The "chapeau de gendarme" sign, also known as "ictal pouting," is a distinctive facial expression observed in focal epilepsy, characterized by a turned-down mouth with symmetrical lip and chin contraction. This systematic review investigate...
Giulia Barbagallo,Giulia Nobile,Maria Grazia Calevo et al. Giulia Barbagallo et al.
Objective: Some children with Childhood Absence Epilepsy (CAE) exhibit focal abnormalities similar to those observed in Self-Limited Focal Epilepsies of Childhood (SeLFEs). It remains unclear whether this subgroup of pati...
Aden P Haskell-Mendoza,Praveen Ramani,Roshni Dhoot et al. Aden P Haskell-Mendoza et al.
Background: Closed-loop responsive neurostimulation (RNS) is an established non-resective neuromodulatory therapy for individuals with drug-resistant epilepsy (DRE). RNS systems are typically programmed to detect and resp...
Vasileios Kokkinos,Stephen A VanHaerents,Cody L Nathan et al. Vasileios Kokkinos et al.
We report ictal SPECT findings in a patient with focal epilepsy and ictal central apnea (ICA). We describe the history, EEG findings, and SPECT analysis of a 38-year-old female with left posterior quadrant epilepsy post intracerebral hemorr...
Melita Cacic Hribljan,Georg Zimmermann,Sándor Beniczky Melita Cacic Hribljan
Objective: To elucidate the lateralizing value of ictal head turning in focal epilepsy and provide guidance for interpreting ictal semiology within the framework of presurgical evaluation. ...
Ramona Cordani,Livia Pisciotta,Michela Stagnaro et al. Ramona Cordani et al.
Background: Alternating Hemiplegia of Childhood (AHC) is a severe channelopathy that manifests before 18 months of age, primarily caused by pathogenic variants in the ATP1A3 gene. It is characterized by recurrent and disa...