Epilepsia Open

Papers
(The median citation count of Epilepsia Open is 1. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2020-03-01 to 2024-03-01.)
ArticleCitations
Glut1 Deficiency Syndrome (Glut1DS): State of the art in 2020 and recommendations of the international Glut1DS study group137
EEG findings in acutely ill patients investigated for SARS‐CoV‐2/COVID‐19: A small case series preliminary report109
Brain‐responsive corticothalamic stimulation in the pulvinar nucleus for the treatment of regional neocortical epilepsy: A case series44
Managing depression and anxiety in people with epilepsy: A survey of epilepsy health professionals by the ILAE Psychology Task Force42
Proposal to optimize evaluation and treatment of Febrile infection‐related epilepsy syndrome (FIRES): A Report from FIRES workshop33
Neurodegenerative pathways as targets for acquired epilepsy therapy development33
Addressing neuropsychological diagnostics in adults with epilepsy: Introducing the International Classification of Cognitive Disorders in Epilepsy: The IC CODE Initiative29
Guidance on Dravet syndrome from infant to adult care: Road map for treatment planning in Europe28
FDA safety warning on the cardiac effects of lamotrigine: An advisory from the Ad Hoc ILAE/AES Task Force28
COX‐2/PGE2 axis regulates hippocampal BDNF/TrkB signaling via EP2 receptor after prolonged seizures26
Management practices for West syndrome in South Asia: A survey study and meta‐analysis25
The gut microbiome in drug‐resistant epilepsy24
Efficacy and safety of perampanel monotherapy in patients with focal‐onset seizures with newly diagnosed epilepsy or recurrence of epilepsy after a period of remission: The open‐label Study 342 (FREED24
Antiepileptogenesis and disease modification: Progress, challenges, and the path forward—Report of the Preclinical Working Group of the 2018 NINDS‐sponsored antiepileptogenesis and disease modificatio23
Phenobarbital as alternate anticonvulsant for organophosphate‐induced benzodiazepine‐refractory status epilepticus and neuronal injury19
Why child neurologists talk about SUDEP: Results from two cross‐sectional surveys18
Serotonin receptors in epilepsy: Novel treatment targets?18
Clinical outcomes and treatments effectiveness in status epilepticus resolved by antiepileptic drugs: A five‐year observational study18
Improving the effectiveness of ANT DBS therapy for epilepsy with optimal current targeting18
Global Survey of Guidelines for the Management of Epilepsy in Pregnancy: A report from the International League Against Epilepsy Task Force on Women and Pregnancy18
Glymphatic system dysfunction in temporal lobe epilepsy patients with hippocampal sclerosis17
Brain‐responsive neurostimulation treatment in patients with GAD65 antibody–associated autoimmune mesial temporal lobe epilepsy16
Impact of diagnostic delay on seizure outcome in newly diagnosed focal epilepsy16
Add‐on cannabidiol significantly decreases seizures in 3 patients with SYNGAP1 developmental and epileptic encephalopathy16
Impact of the COVID‐19 lockdown on patients and families with Dravet syndrome15
Epileptic spasms in individuals with Down syndrome: A review of the current literature15
Antiepileptogenesis and disease modification: Clinical and regulatory issues15
Sleep‐wake characteristics in a mouse model of severe traumatic brain injury: Relation to posttraumatic epilepsy14
Ceribell EEG shortens seizure diagnosis and workforce time and is useful for COVID isolation14
Real‐world safety and effectiveness of cenobamate in patients with focal onset seizures: Outcomes from an Expanded Access Program14
An examination of the efficacy and safety of fenfluramine in adults, children, and adolescents with Dravet syndrome in a real‐world practice setting: A report from the Fenfluramine European13
A retrospective, real‐world experience of perampanel monotherapy in patient with first new onset focal seizure: A Thailand experience13
Driving a motor vehicle and psychogenic nonepileptic seizures: ILAE Report by the Task Force on Psychogenic Nonepileptic Seizures13
Real‐world data on cannabidiol treatment of various epilepsy subtypes: A retrospective, multicenter study13
Validation of EpiTRAQ, a transition readiness assessment tool for adolescents and young adults with epilepsy13
Transporter hypothesis in pharmacoresistant epilepsies. Is it at the central or peripheral level?13
On the clinical acceptance of black‐box systems for EEG seizure prediction12
Biodegradable nanoparticles for the treatment of epilepsy: From current advances to future challenges12
PROVE: Retrospective, non‐interventional, Phase IV study of perampanel in real‐world clinical care of patients with epilepsy12
Daily listening to Mozart reduces seizures in individuals with epilepsy: A randomized control study12
A retrospective review of changes and challenges in the use of antiseizure medicines in Dravet syndrome in Norway12
Stereotactic laser interstitial thermal therapy corpus callosotomy for the treatment of pediatric drug‐resistant epilepsy12
EEG datasets for seizure detection and prediction— A review12
sEEG for expansion of a surgical epilepsy program: Safety and efficacy in 152 consecutive cases11
Acetazolamide: Old drug, new evidence?11
Development and validation of the Epilepsy Self‐Stigma Scale11
One‐year cost‐effectiveness of callosotomy vs vagus nerve stimulation for drug‐resistant seizures in Lennox‐Gastaut Syndrome: A decision analytic model11
The opioid antagonist naltrexone decreases seizure‐like activity in genetic and chemically induced epilepsy models11
Newly diagnosed seizures assessed at two established first seizure clinics: Clinic characteristics, investigations, and findings over 11 years11
Coupling between infraslow activities and high‐frequency oscillations precedes seizure onset10
Developmental and epileptic encephalopathy: Personal utility of a genetic diagnosis for families10
Brain‐Responsive Neurostimulation for the treatment of adults with epilepsy in tuberous sclerosis complex: A case series10
How much time is enough? Establishing an optimal duration of recording for ambulatory video EEG10
Detection of anomalous high‐frequency events in human intracranial EEG10
Combination of antiseizure medications phenobarbital, ketamine, and midazolam reduces soman‐induced epileptogenesis and brain pathology in rats10
Behavioral phenotypes of temporal lobe epilepsy9
Systemic and cerebrospinal fluid immune and complement activation in Ugandan children and adolescents with long‐standing nodding syndrome: A case‐control study9
Medical treatment in infants and young children with epilepsy: Off‐label use of antiseizure medications. Survey Report of ILAE Task Force Medical Therapies in Children9
Clinical and genetic characteristics of patients with Doose syndrome8
Classifying etiology of infantile spasms syndrome in resource‐limited settings: A study from the South Asian region8
The role of efflux transporters and metabolizing enzymes in brain and peripheral organs to explain drug‐resistant epilepsy8
Semiology of spontaneous generalized tonic‐clonic seizures in the epileptic baboon8
Post‐acute symptomatic seizure (PASS) clinic: A continuity of care model for patients impacted by continuous EEG monitoring8
The epileptogenic zone in children with tuberous sclerosis complex is characterized by prominent features of focal cortical dysplasia8
Long‐term safety and tolerability of lacosamide monotherapy in patients with epilepsy: Results from a multicenter, open‐label trial8
Epilepsy in Morocco: Realities, pitfalls and prospects8
Experience of perampanel monotherapy beyond initial titration to achieve seizure freedom in patients with focal‐onset seizures with newly diagnosed or currently untreated recurrent epilepsy: A post ho8
Therapeutic drug monitoring of perampanel in children diagnosed with epilepsy: Focus on influencing factors on the plasma concentration‐to‐dose ratio8
Sevoflurane as bridge therapy for plasma exchange and Anakinra in febrile infection–related epilepsy syndrome8
Diurnal burden of spontaneous seizures in early epileptogenesis in the post‐kainic acid rat model of epilepsy8
Predictors of high school dropout, anxiety, and depression in genetic generalized epilepsy8
Late diagnoses of Dravet syndrome: How many individuals are we missing?8
Multimodal nocturnal seizure detection: Do we need to adapt algorithms for children?8
Performance of ECG‐based seizure detection algorithms strongly depends on training and test conditions8
Astrocyte reactivity in a mouse model of SCN8A epileptic encephalopathy8
A complex systems view on the current hypotheses of epilepsy pharmacoresistance7
Availability, affordability, and quality of essential antiepileptic drugs in Lao PDR7
Screening of prototype antiseizure and anti‐inflammatory compounds in the Theiler's murine encephalomyelitis virus model of epilepsy7
Deep brain stimulation of the centromedian thalamic nucleus for the treatment of FIRES7
Long‐term outcomes after NORSE: Treatment with vagus nerve stimulation7
Seizures in Sotos syndrome: Phenotyping in 49 patients7
Open‐label long‐term treatment of add‐on triheptanoin in adults with drug‐resistant epilepsy7
Clemizole and trazodone are effective antiseizure treatments in a zebrafish model of STXBP1 disorder7
Efficacy and safety of adjunctive padsevonil in adults with drug‐resistant focal epilepsy: Results from two double‐blind, randomized, placebo‐controlled trials7
Optimizing the surgical management of MRI‐negative epilepsy in the neuromodulation era7
ResectVol: A tool to automatically segment and characterize lacunas in brain images7
Perampanel in real‐world clinical care of patients with epilepsy: Interim analysis of a phase IV study7
Epilepsy phenotype in individuals with chromosomal duplication encompassing FGF127
Consistent safety and tolerability of Valtoco® (diazepam nasal spray) in relationship to usage frequency in patients with seizure clusters: Interim results from a phase 3, long‐term, open‐l7
Clinical and genomic analysis of a large Chinese family with familial cortical myoclonic tremor with epilepsy and SAMD12 intronic repeat expansion7
Demonstrating the feasibility of digital health to support pediatric patients in South Africa7
Efficacy of long‐term adrenocorticotropic hormone therapy for West syndrome: A retrospective multicenter case series7
Effectiveness of perampanel as the only add‐on: Retrospective, multicenter, observational real‐life study on epilepsy patients7
Scalp HFO rates are higher for larger lesions7
Multi‐omic strategies applied to the study of pharmacoresistance in mesial temporal lobe epilepsy6
Prevalence of epilepsy in Bangladesh: Results from a national household survey6
Status epilepticus in the Canadian Arctic: A public health imperative hidden in plain sight6
Seizures induced in electroconvulsive therapy as a human epilepsy model: A comparative case study6
A disease concept model for STXBP1‐related disorders6
Impact of COVID‐19 pandemic on epilepsy care in Japan: A national‐level multicenter retrospective cohort study6
Long‐term open‐label perampanel: Generalized tonic–clonic seizures in idiopathic generalized epilepsy6
Potential role of FKBP5 single‐nucleotide polymorphisms in functional seizures6
Effect of fenfluramine on seizures and comorbidities in SCN8A‐developmental and epileptic encephalopathy: A case series6
KETASER01 protocol: What went right and what went wrong6
Seizure‐related injuries in people with epilepsy: A cohort study from Saudi Arabia6
Sex‐based structural and functional MRI outcomes in the rat brain after soman (GD) exposure‐induced status epilepticus6
Use of suggestive seizure manipulation methods in the investigation of patients with possible psychogenic nonepileptic seizures—An international ILAE survey6
Epilepsy in the Sanaga‐Mbam valley, an onchocerciasis‐endemic region in Cameroon: electroclinical and neuropsychological findings6
A novel FAME1 repeat configuration in a European family identified using a combined genomics approach6
Dravet syndrome: A systematic literature review of the illness burden5
Intracranial monitoring contributes to seizure freedom for temporal lobectomy patients with nonconcordant preoperative data5
Status of epilepsy in the tropics: An overlooked perspective5
Epilepsy duration is an independent factor for electrocardiographic changes in pediatric epilepsy5
Drug‐resistant epilepsy and the hypothesis of intrinsic severity: What about the high‐frequency oscillations?5
Experience with the ketogenic diet in premature neonates5
Familial neonatal seizures caused by the Kv7.3 selectivity filter mutation T313I5
Neurodevelopmental origins of self‐limiting rolandic epilepsy: Systematic review of MR imaging studies5
Factors not considered in the study of drug‐resistant epilepsy: Psychiatric comorbidities, age, and gender5
Recurrence risk after a first remote symptomatic seizure in adults: Epilepsy or not?5
A European pilot study in Dravet Syndrome to delineate what really matters for the patients and families5
Sleep architecture in drug‐naïve adult patients with epilepsy: Comparison between focal and generalized epilepsy5
A cross‐sectional study of COVID‐19 vaccination patterns among patients with epilepsy in Hong Kong5
Knowledge and attitude toward epilepsy among the final and semi‐final years medical students at University of Bahri, Sudan5
A new rapid titration protocol for lamotrigine that reduces the risk of skin rash5
A novel possible familial cause of epilepsy of infancy with migrating focal seizures related to SZT2 gene variant5
Brain glycogen content is increased in the acute and interictal chronic stages of the mouse pilocarpine model of epilepsy5
Interpretable deep learning‐based hippocampal sclerosis classification5
Validation of semi‐automated anatomically labeled SEEG contacts in a brain atlas for mapping connectivity in focal epilepsy5
Analyses of seizure responses supportive of a novel trial design to assess efficacy of antiepileptic drugs in infants and young children with epilepsy: Post hoc analyses of pediatric levetiracetam and5
Factors not considered in the study of drug‐resistant epilepsy: Drug‐resistant epilepsy: Assessment of neuroinflammation5
A study of factors influencing self‐stigma in people with epilepsy: A nationwide online questionnaire survey in Japan5
Early preclinical plasma protein biomarkers of brain trauma are influenced by early seizures and levetiracetam4
Delta brush variant: A novel ictal EEG pattern in anti‐NMDAR encephalitis4
Use of the International League Against Epilepsy (ILAE) 1989, 2010, and 2017 Classification of Epilepsy in children in a low‐resource setting: A hospital‐based cross‐sectional study4
Epilepsy surgery in early infancy: A retrospective, multicenter study4
Assessment and treatment of childhood epilepsy in Haiti4
Combined use of the ketogenic diet and vagus nerve stimulation in pediatric drug‐resistant epilepsy4
Clinical characteristics and outcomes after new‐onset seizure among Zambian children with HIV during the antiretroviral therapy era4
Microglia and status epilepticus in the immature brain4
Recurrence rates and risk factors for seizure recurrence following antiseizure medication withdrawal in adolescent patients with genetic generalized epilepsy4
Treatment of cholinergic‐induced status epilepticus with polytherapy targeting GABA and glutamate receptors4
The Efficacy, Safety, and Outcomes of Brain‐responsive Neurostimulation (RNS® System) therapy in older adults4
Infantile‐onset myoclonic developmental and epileptic encephalopathy: A new RARS2 phenotype4
Impact of theCOVID‐19 pandemic on people with epilepsy: Findings from theUSarm of theCOV‐Estudy4
FKBP5 blockade may provide a new horizon for the treatment of stress‐associated disorders: An in‐silico study4
Cardiac structural and functional abnormalities in epilepsy: A systematic review and meta‐analysis4
Comorbid seizure reduction after pallidothalamic tractotomy for movement disorders: Revival of Jinnai’s Forel‐H‐tomy4
Barriers to generic antiseizure medication use: Results of a global survey by the International League Against Epilepsy Generic Substitution Task Force4
Are we responding effectively to bone mineral density loss and fracture risks in people with epilepsy?4
Human herpesvirus 6 and epilepsy4
Frontal disconnection surgery for drug‐resistant epilepsy: Outcome in a series of 16 patients4
An online tool for information to women with epilepsy and therapeutic drug monitoring in pregnancy: Design and pilot study4
The National Comprehensive Governance for epilepsy prevention and control in China4
Risk factors that predict delayed seizure detection on continuous electroencephalogram (cEEG) in a large sample size of critically ill patients4
Drug‐resistant epilepsy: Drug target hypothesis and beyond the receptors4
A team science approach to discover novel targets for infantile spasms (IS)3
Intraperitoneal injection of lipopolysaccharide prevents seizure‐induced respiratory arrest in a DBA/1 mouse model of SUDEP3
Integrating metabolomics and lipidomics revealed a decrease in plasma fatty acids but an increase in triglycerides in children with drug‐refractory epilepsy3
Confirmation of infantile spasms resolution by prolonged outpatient EEGs3
Evidence for long memory in focal seizure duration3
Sudden unexpected death in epilepsy: A critical view of the literature3
The efficacy and safety of adjunctive perampanel for the treatment of refractory focal‐onset seizures in patients with epilepsy: A meta‐analysis3
Epileptic Status in a PEDiatric cohort (ESPED) requiring intensive care treatment: A multicenter, national, two‐year prospective surveillance study3
Takotsubo stress cardiomyopathy following explantation of sEEG electrodes3
Knowledge and misconceptions about epilepsy among people with epilepsy and their caregivers attending mental health clinics: A qualitative study in Taenia solium endemic pig‐keeping communities3
Complete hemispherotomy leads to lateralized functional organization and lower level of consciousness in the isolated hemisphere3
2‐deoxyglucose and β‐hydroxybutyrate fail to attenuate seizures in the betamethasone‐NMDA model of infantile spasms3
Parental perception of FIRES outcomes, emotional states, and social media usage3
Ordinal regression increases statistical power to predict epilepsy surgical outcomes3
Optimal timing of interictal FDG‐PET for epilepsy surgery: A systematic review on time since last seizure3
Availability, affordability, and quality of essential anti‐seizure medication in Cambodia3
Evaluation of the International League Against Epilepsy 1981, 1989, and 2017 classifications of seizure semiology and etiology in a population‐based cohort of children and adults with epilepsy3
Safety and adverse events following COVID‐19 vaccination among people with epilepsy: A cross‐sectional study3
Seizure features and outcomes in 50 children with GATOR1 variants: A retrospective study, more favorable for epilepsy surgery3
Brivaracetam substituting other antiepileptic treatments: Results of a retrospective study in German epilepsy centers3
Assessing the role of ketogenic dietary therapy in ring chromosome 20 syndrome: A patient‐led approach3
Anxiety and depressive symptoms in adults with new‐onset seizures: A scoping review3
Clinical profile and treatment outcome of epilepsy syndromes in children: A hospital‐based study in Eastern Nepal3
The goal of explaining black boxes in EEG seizure prediction is not to explain models' decisions3
Predictors of outcomes after surgery for medically intractable insular epilepsy: A systematic review and individual participant data meta‐analysis3
Quality of life among caregivers of children with epilepsy: A cross‐sectional study at Eastern Nepal3
Interictal pattern on scalp electroencephalogram predicts excellent surgical outcome of epilepsy caused by focal cortical dysplasia3
Hyperventilation maneuver during EEG in children with epilepsy after the COVID‐19 pandemic. Is a routine procedure necessary?3
The efficacy and safety of ganaxolone for the treatment of refractory epilepsy: A meta‐analysis from randomized controlled trials3
Programmed mechanisms of status epilepticus‐induced neuronal necrosis3
Genetic generalized epilepsies with frontal lesions mimicking migratory disorders on the epilepsy monitoring unit3
How accurately do adult patients report their absence seizures?3
Status epilepticus and early development: Neuronal injury, neurodegeneration, and their consequences3
The AMPA receptor antagonist perampanel suppresses epileptic activity in human focal cortical dysplasia3
Termination of seizures by ictal transcranial focal cortex stimulation3
Real‐world analysis of hospitalizations in patients with epilepsy and treated with perampanel3
Progressive myoclonus epilepsies due to SEMA6B mutations. New variants and appraisal of published phenotypes3
Asymmetric epileptic spasms after corpus callosotomy in children with West syndrome may be a good indicator for unilateral epileptic focus and subsequent resective surgery3
A registry for Dravet syndrome: The Italian experience3
Pregabalin as adjunctive therapy in adult and pediatric patients with generalized tonic‐clonic seizures: A randomized, placebo‐controlled trial3
Musicogenic reflex seizure with positive antiglutamic decarboxylase antibody: A case report3
Efficacy and safety of adjunctive perampanel in patients with focal seizures or generalized tonic‐clonic seizures: Post hoc analysis of Phase II and Phase III double‐blind and open‐label extension stu3
Deep‐learning predicted PET can be subtracted from the true clinical fluorodeoxyglucose PET co‐registered to MRI to identify the epileptogenic zone in focal epilepsy3
Creation and implementation of an electronic health record note for quality improvement in pediatric epilepsy: Practical considerations and lessons learned2
The effects of COVID‐19 measures on the hospitalization of patients with epilepsy and status epilepticus in Thailand: An interrupted time series analysis2
Clinical characteristics of epilepsy in resource‐limited communities in Punjab, Northwest India2
How the characteristics of pediatric neurologists in Latin America influence the communication of sudden unexpected death in epilepsy to patients and caregivers2
An epidemiological survey of epilepsy in tropical rural areas of China2
Landscape of genetic infantile epileptic spasms syndrome—A multicenter cohort of 124 children from India2
Focal impaired awareness seizures in a rodent model: A functional anatomy2
Epilepsy is an important feature of KBG syndrome associated with poorer developmental outcome2
Unfavorable public attitude toward people with epilepsy in Ethiopia: A systematic review and meta‐analysis study2
The epilepsy phenotype of ST3GAL3‐related developmental and epileptic encephalopathy2
Dyscalculia and dyslexia in Chinese children with idiopathic epilepsy: Different patterns of prevalence, comorbidity, and gender differences2
Prospective study of cenobamate on cognition, affectivity, and quality of life in focal epilepsy2
An approach for reliably identifying high‐frequency oscillations and reducing false‐positive detections2
Cannabidiol in the acute phase of febrile infection‐related epilepsy syndrome (FIRES)2
Neuropsychiatric profile in average intelligent individuals with coexisting epilepsy and psychogenic non‐epileptic seizures2
A cluster‐randomized trial comparing home‐based primary health care and usual clinic care for epilepsy in a resource‐limited country2
Experimental status epilepticus, COX‐2 and BDNF: Connecting the dots2
Epilepsy classification using artificial intelligence: A web‐based application2
Identification and clinical characteristics of a novel missense ADGRG1 variant in bilateral Frontoparietal Polymicrogyria: The electroclinical change from infancy to adulthood after Calloso2
COL4A1 mutation‐related disorder presenting as fetal intracranial bleeding, hydrocephalus, and polymicrogyria2
Predictors of outcome in refractory generalized convulsive status epilepticus2
Relationship between right‐to‐left shunt, hypoxia, and epilepsy2
Final analysis of potential drug–drug interactions between highly purified cannabidiol and anti‐seizure medications in an open‐label expanded access program2
“The understanding and attitude toward epilepsy in the Souss‐Massa region of Morocco”2
Treatment of status epilepticus: Physiology, pharmacology, and future directions2
Assessment of self‐stigma in epilepsy: Validation of the German version Epilepsy Self‐Stigma Scale (ESSS‐G)2
Prevalence of epilepsy in the rural area of the Bolivian Gran Chaco: Usefulness of telemedicine and impact of awareness campaigns2
Antiepileptogenesis after stroke—trials and tribulations: Methodological challenges and recruitment results of a Phase II study with eslicarbazepine acetate2
Ictal and interictalSPECTwith99mTc‐HMPAOin presurgical epilepsy. I: Predictive value and methodological considerations2
Ictal and interictal SPECT with 99mTc‐HMPAO in presurgical epilepsy. II: Methodological considerations on hyper‐ and hypoperfusion2
The clinical analysis of new‐onset status epilepticus2
Periictal water drinking revisited: Occurrence and lateralizing value in surgically confirmed patients with focal epilepsy2
Assessment of tau phosphorylation and β‐amyloid pathology in human drug‐resistant epilepsy2
Differences between men and women in response to antiseizure medication use and the likelihood of developing treatment resistant epilepsy2
Fractures in people with epilepsy: A nationwide population‐based cohort study2
A survey of the European Reference Network EpiCARE on clinical practice for selected rare epilepsies2
Antiseizure medication discovery: Recent and future paradigm shifts2
Different pharmacoresistance of focal epileptic spasms, generalized epileptic spasms, and generalized epileptic spasms combined with focal seizures2
Timing differences between HFOs and interictal epileptiform discharges generated in vitro by different mechanisms in rat hippocampal slices: A novel approach2
Frequency of and factors associated with antiseizure medication discontinuation discussions and decisions in patients with epilepsy: A multicenter retrospective chart review2
Child neurology services for children with epilepsy in Finland1
The causal effect of serum 25‐hydroxyvitamin D levels on epilepsy: A two‐sample Mendelian randomization study1
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Causal relationship between telomere length and epilepsy: A bidirectional Mendelian randomization study1
A companion to the preclinical common data elements for genomics, transcriptomics, and epigenomics data in rodent epilepsy models. A report of the TASK3‐WG4 omics working group of the 1
Temporal encephaloceles and coexisting epileptogenic lesions1
Capturing seizures in clinical trials of antiseizure medications for KCNQ2‐DEE1
3D figure of epilepsy syndromes1
A companion to the preclinical common data elements for rodent genetic epilepsy models. A report of the TASK3‐WG1B: Paediatric and genetic models working group of the ILAE/A1
Morphometric analysis program: Detection of epileptic foci in young children using an adult normative database: Initial experience1
A companion to the preclinical common data elements for proteomics, lipidomics, and metabolomics data in rodent epilepsy models. A report of the TASK3‐WG4 omics working group of the ILAE/AES joint tra1
Man and the machine rise to the spike‐wave. Commentary on “An automated, machine learning‐based detection algorithm for spike‐wave discharges (SWDs) in a mouse model of absence epilepsy.”1
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