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Subject Areas on Research
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"Walking the Journey Together": Creating a unique learning module in provider-patient communication for the care of epilepsy in Uganda.
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2018 ACC/AHA/HRS Guideline on the Evaluation and Management of Patients With Bradycardia and Cardiac Conduction Delay: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines and the Heart Rhythm Society.
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A Closed Loop Brain-machine Interface for Epilepsy Control Using Dorsal Column Electrical Stimulation.
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A Peptide Uncoupling BDNF Receptor TrkB from Phospholipase Cγ1 Prevents Epilepsy Induced by Status Epilepticus.
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A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutations.
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A design for the prospective evaluation of the efficacy and toxicity of antiepileptic drugs in adults.
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A method of quantification for the evaluation of antiepileptic drug therapy.
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A point mutation (D79N) of the alpha2A adrenergic receptor abolishes the antiepileptogenic action of endogenous norepinephrine.
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A review on the management of epilepsy associated with hypothalamic hamartomas.
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A syndrome of autosomal dominant alternating hemiplegia: clinical presentation mimicking intractable epilepsy; chromosomal studies; and physiologic investigations.
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A television fluorometer for monitoring oxidative metabolism in intact tissue.
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ACR Appropriateness Criteria® Seizures and Epilepsy.
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Abnormal moral reasoning in complete and partial callosotomy patients.
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Actions from thoughts.
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Adaptation of high-gamma responses in human auditory association cortex.
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Aligning animal models with clinical epilepsy: where to begin?
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Altered morphology of hippocampal dentate granule cell presynaptic and postsynaptic terminals following conditional deletion of TrkB.
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An Analysis of Public Interest in Elective Neurosurgical Procedures During the COVID-19 Pandemic Through Online Search Engine Trends.
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An NMDA-mediated component of excitatory synaptic input to dentate granule cells in 'epileptic' human hippocampus studied in vitro.
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Analyses of the molecular basis of kindling development.
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Anticonvulsant and antiepileptogenic actions of MK-801 in the kindling and electroshock models.
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Antiepileptic drugs prevent seizures in hyperbaric oxygen: A novel model of epileptiform activity.
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Antiepileptogenesis and disease modification: Clinical and regulatory issues.
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Antiepileptogenic effects of conventional anticonvulsants in the kindling model of epilespy.
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Antiseizure Medication Withdrawal in Seizure-Free Patients: Practice Advisory Update Summary: Report of the AAN Guideline Subcommittee.
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Antiseizure medication use and medical resource utilization after resective epilepsy surgery in children in the United States: A contemporary nationwide cross-sectional cohort analysis.
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Approach to epilepsy in children.
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Approach to pediatric epilepsy surgery: State of the art, Part I: General principles and presurgical workup.
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Approach to pediatric epilepsy surgery: State of the art, Part II: Approach to specific epilepsy syndromes and etiologies.
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Arrhythmogenic epilepsy: an hypothesis.
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Association Between Standardized Mortality Ratio and Utilization of Care in US Veterans With Drug-Resistant Epilepsy Compared With All US Veterans and the US General Population.
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Association of Transition Readiness to Intentional Self-Regulation and Hopeful Future Expectations in Youth With Illness.
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Association of guideline publication and delays to treatment in pediatric status epilepticus.
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Attenuation of epileptiform bursting by baclofen: reduced potency in elevated potassium.
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Attenuation of epileptogenesis: proactive effect of a single epinephrine injection of amygdaloid kindling.
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Axon terminal hyperexcitability associated with epileptogenesis in vitro. I. Origin of ectopic spikes.
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Axon terminal hyperexcitability associated with epileptogenesis in vitro. II. Pharmacological regulation by NMDA and GABAA receptors.
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Axon terminal hyperexcitability seen in epileptogenesis in vitro.
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B cells and epilepsy: the odd couple.
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Baclofen has a proepileptic effect in the rat dentate gyrus.
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Baclofen suppresses bursting activity induced in hippocampal slices by differing convulsant treatments.
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Baclofen suppresses hippocampal epileptiform activity at low concentrations without suppressing synaptic transmission.
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Barriers and facilitators to implementation of epilepsy self-management programs: a systematic review using qualitative evidence synthesis methods.
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Barriers to biomedical care for people with epilepsy in Uganda: A cross-sectional study.
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Behavioral side effects of gabapentin in children.
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Biochemical and radiohistochemical analyses of alpha-2 adrenergic receptors in the kindling model of epilepsy.
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Biomarkers aiding diagnosis of atypical presentation of pyridoxine-dependent epilepsy.
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Brain migration disorder and T-cell activation deficiency associated with abnormal signaling through TCR/CD3 complex and hyperactivity of Fyn tyrosine kinase.
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CYP2C9*1B promoter polymorphisms, in linkage with CYP2C19*2, affect phenytoin autoinduction of clearance and maintenance dose.
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Callosal alterations in pyridoxine-dependent epilepsy.
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Calmodulin limits pathogenic Na+ channel persistent current.
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Can you predict an immediate, complete, and sustained response to the ketogenic diet?
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Cannabis Use Disorder and Epilepsy: A Cross-National Analysis of 657 072 Hospitalized Patients.
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Carbamazepine increases phenytoin serum concentration and reduces phenytoin clearance.
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Cardiac Dysfunction After Neurologic Injury: What Do We Know and Where Are We Going?
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Causes of treatment failure with antiepileptic drugs vary over time.
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Cellular and molecular basis of epilepsy.
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Cerebral hypervascularity and early venous opacification in status epilepticus. A case report.
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Cerebral lateralization of neuronal activity during naming, reading and line-matching.
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Changes in gamma-aminobutyric acid and somatostatin in epileptic cortex associated with low-grade gliomas.
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Characteristics of Neonates with Cardiopulmonary Disease Who Experience Seizures: A Multicenter Study.
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Classification of epilepsy syndromes and role of genetic factors.
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Clinical Features, Neuropathology, and Surgical Outcome in Patients With Refractory Epilepsy and Brain Somatic Variants in the SLC35A2 Gene.
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Clinical applications of neuroimaging in psychiatry.
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Clinical prospects for neural grafting therapy for hippocampal lesions and epilepsy.
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Clinical utility of genetic testing in pediatric drug-resistant epilepsy: a pilot study.
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Clinically significant bradyarrhythmias in video-EEG patients.
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Commentary: a new era in epilepsy care. Guidelines address first steps in diagnosis and treatment.
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Comparative efficacy of antiepileptic drugs.
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Comparison of brand versus generic antiepileptic drug adverse event reporting rates in the U.S. Food and Drug Administration Adverse Event Reporting System (FAERS).
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Comparison of carbamazepine, phenobarbital, phenytoin, and primidone in partial and secondarily generalized tonic-clonic seizures.
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Complex genetic disease: can genetic strategies in Alzheimer's disease and new genetic mechanisms be applied to epilepsy?
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Complex neuronal systems: approach to development of new strategies in the treatment of epilepsy.
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Comprehensive presurgical functional MRI language evaluation in adult patients with epilepsy.
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Conditional deletion of TrkB but not BDNF prevents epileptogenesis in the kindling model.
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Conditional deletion of TrkC does not modify limbic epileptogenesis.
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Connectomics and graph theory analyses: Novel insights into network abnormalities in epilepsy.
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Consensus guidelines for the diagnosis and management of pyridoxine-dependent epilepsy due to α-aminoadipic semialdehyde dehydrogenase deficiency.
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Contemporaneous evaluation of patient experience, surgical strategy, and seizure outcomes in patients undergoing stereoelectroencephalography or subdural electrode monitoring.
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Conversational analysis of consciousness during seizures.
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Core elements of epilepsy diagnosis and management: expert consensus from the Leadership in Epilepsy, Advocacy, and Development (LEAD) faculty.
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Corpus Callosum Diffusion and Connectivity Features in High Functioning Subjects With Pyridoxine-Dependent Epilepsy.
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Correlation between function and structure in "epileptic" human hippocampal tissue maintained in vitro.
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Correlation of 99mTc-HMPAO SPECT with EEG monitoring: prognostic value for outcome of epilepsy surgery in children.
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Cortical Language Areas and Plasticity in Pediatric Patients With Epilepsy: A Review.
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Cost-effectiveness of HLA-B*1502 genotyping in adult patients with newly diagnosed epilepsy in Singapore.
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Cost-effectiveness of HLA-B*1502 genotyping in adult patients with newly diagnosed epilepsy in Singapore.
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Cross-correlation based μECoG waveform tracking.
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Current and Emerging Surgical Therapies for Severe Pediatric Epilepsies.
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Data mining neocortical high-frequency oscillations in epilepsy and controls.
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De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies.
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De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis.
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De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy.
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De novo variants in the alternative exon 5 of SCN8A cause epileptic encephalopathy.
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Decoding individual finger movements from one hand using human EEG signals.
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Development of new pharmacological agents for epilepsy: lessons from the kindling model.
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Developmental outcome in pyridoxine-dependent epilepsy: Better late (onset) than early.
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Differential diagnosis of staring spells in children: a video-EEG study.
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Differential effects of phenobarbital and pentobarbital on stimulus train-induced bursting in the hippocampal slice.
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Differential expression of GABA and glutamate-receptor subunits and enzymes involved in GABA metabolism between electrophysiologically identified hippocampal CA1 pyramidal cells and interneurons.
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Differential expression of immediate early genes in the hippocampus in the kindling model of epilepsy.
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Differentiation of Epileptic and Psychogenic Nonepileptic Seizures Using Single-Channel Surface Electromyography.
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Discontinuing antiepileptic drugs in children with epilepsy. A comparison of a six-week and a nine-month taper period.
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Discovery and development of lamotrigine for bipolar disorder: a story of serendipity, clinical observations, risk taking, and persistence.
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Disrupting abnormal electrical activity with deep brain stimulation: is epilepsy the next frontier?
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Disruption of Fgf13 causes synaptic excitatory-inhibitory imbalance and genetic epilepsy and febrile seizures plus.
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Disruption of TrkB-mediated phospholipase Cgamma signaling inhibits limbic epileptogenesis.
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Diverse genetic causes of polymicrogyria with epilepsy.
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Do prolonged febrile seizures produce medial temporal sclerosis? Hypotheses, MRI evidence and unanswered questions.
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Does epileptiform activity contribute to cognitive impairment in Alzheimer's disease?
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Does the teddy bear sign predict psychogenic nonepileptic seizures?
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Double-blind randomized study comparing brand-name and generic phenytoin monotherapy.
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Dramatic Response After Lamotrigine in a Patient With Epileptic Encephalopathy and a De NovoCACNA1A Variant.
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Drosophila as a model for epilepsy: bss is a gain-of-function mutation in the para sodium channel gene that leads to seizures.
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Early onset severe ATP1A2 epileptic encephalopathy: Clinical characteristics and underlying mutations.
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Early-life epilepsy after acute symptomatic neonatal seizures: A prospective multicenter study.
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Effect of antiepileptic drugs on bone density in ambulatory patients.
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Effect of high doses of intravenously administered immune globulin on natural killer cell activity in peripheral blood.
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Effects of diisopropyl phosphorofluoridate (DFP) on CA3 and CA1 responses in rat hippocampus.
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Effects of epilepsy surgery on quality of life: a controlled study in a Middle Eastern population.
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Effects of potassium on oxidative metabolism and seizures.
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Effects of religiosity and religious coping on medication adherence and quality of life among people with epilepsy.
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Electroencephalographic and seizure manifestations of pyridoxal 5'-phosphate-dependent epilepsy.
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Emergency management of the patient with seizures. 1. Classification and treatment system, common seizure disorders.
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Emergency management of the patient with seizures. 1. Generalized status epilepticus.
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Emerging insights into the genesis of epilepsy.
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Empirically Based Guidelines for Selecting Vagus Nerve Stimulation Parameters in Epilepsy and Heart Failure.
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Epilepsy and neurocysticercosis: an incidence study in a Peruvian rural population.
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Epilepsy associated with lupus anticoagulant.
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Epilepsy beliefs and misconceptions among patient and community samples in Uganda.
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Epilepsy due to 20q13.33 subtelomere deletion masquerading as pyridoxine-dependent epilepsy.
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Epilepsy genetics: an abundance of riches for biologists.
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Epilepsy in KCNH1-related syndromes.
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Epilepsy in neurofibromatosis type 1.
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Epilepsy surgery in a developing country (Lebanon): ten years experience and predictors of outcome.
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Epilepsy.
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Epilepsy.
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Epilepsy: A Disruptive Force in History.
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Epileptic and electroencephalographic manifestations of guanidinoacetate-methyltransferase deficiency.
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Epileptic cell damage and epileptogenesis. Introduction.
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Epileptic encephalopathy with features of rapid-onset dystonia Parkinsonism and alternating hemiplegia of childhood: a novel combination phenotype associated with ATP1A3 mutation.
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Epileptiform discharges triggered with direct electrical stimulation for treatment-resistant depression: Factors that modulate risk and treatment considerations.
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Epinephrine proactive retardation of amygdala-kindled epileptogenesis.
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Ergot, the "jerks," and revivals.
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Ethical challenges in genotype-driven research recruitment.
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Evaluation of Proactive Community Case Detection to Increase Help Seeking for Mental Health Care: A Pragmatic Randomized Controlled Trial.
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Evaluation of a tailored epilepsy training program for healthcare providers in Uganda.
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Evaluation of complication rates of pediatric cranial procedures in which a polyethylene glycol sealant was used.
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Excitatory amino acid receptors and epilepsy.
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Excitatory amino acid receptors in epilepsy.
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Expanding spectrum of paroxysmal events in children: potential mimickers of epilepsy.
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Experimental thalamic epileptic discharge.
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Extratemporal resective surgery for epilepsy.
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Facioscapulohumeral muscular dystrophy can be a cause of isolated childhood cognitive dysfunction.
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Factors associated with patients not proceeding with proposed resective epilepsy surgery.
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Fascicles split or merge every ∼560 microns within the human cervical vagus nerve.
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Flunarizine for treatment of partial seizures: results of a concentration-controlled trial.
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Fluorometric monitoring of NADH levels in cerebral cortex: preliminary observations in human epilepsy.
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Foundation and practice of neurofeedback for the treatment of epilepsy.
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Functional recovery following resection of an epileptogenic focus in the motor hand area.
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Furosemide and mannitol suppression of epileptic activity in the human brain.
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Gap junctional intercellular communication in hypoxia-ischemia-induced neuronal injury.
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Gene markers in brain tumors: what the epileptologist should know.
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Genes with high penetrance for syndromic and non-syndromic autism typically function within the nucleus and regulate gene expression.
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Genetic and environmental correlates of topiramate-induced cognitive impairment.
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Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies.
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Genetic modifiers of the Kv beta2-null phenotype in mice.
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Genetics of pediatric epilepsy.
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Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies.
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Genomic analysis of "microphenotypes" in epilepsy.
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Genotype-phenotype correlation of congenital anomalies in multiple congenital anomalies hypotonia seizures syndrome (MCAHS1)/PIGN-related epilepsy.
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Geometric morphometrics reveal altered corpus callosum shape in pyridoxine-dependent epilepsy.
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Glial localization of antiquitin: implications for pyridoxine-dependent epilepsy.
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Glutamate receptor autoimmunity in Rasmussen's encephalitis.
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Growth Associated Protein 43 (GAP-43) as a Novel Target for the Diagnosis, Treatment and Prevention of Epileptogenesis.
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Guideline and algorithms for treatment of pediatric epilepsy in the West: how about the individual patient and the rest of the world?
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Guideline twelve: guidelines for long-term monitoring for epilepsy.
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Guideline twelve: guidelines for long-term monitoring for epilepsy.
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Healthcare provider perspectives regarding epilepsy care in Uganda.
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Hereditary long Q-T syndrome presenting as epilepsy: electroencephalography laboratory diagnosis.
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Hippocampal epileptiform activity induced by magnesium-free medium: differences between areas CA1 and CA2-3.
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Hospital-based epilepsy care in Uganda: A prospective study of three major public referral hospitals.
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Hub GABA neurons mediate gamma-frequency oscillations at ictal-like event onset in the immature hippocampus.
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Hysterical psychosis and epilepsy: differential diagnosis.
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Hysteroepilepsy in the nineteenth century: Charcot and Gowers.
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Identification of early recurrence of primary central nervous system tumors by [18F]fluorodeoxyglucose positron emission tomography.
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Identification of genetic defect of an epilepsy: strategies for therapeutic advances.
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Imaging findings of structural causes of epilepsy in children: a guide for the radiologist in the emergency room.
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Imaging of intrinsic optical signals in primate cortex during epileptiform activity.
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Implementation of an established algorithm and modifications for the identification of epilepsy patients in the veterans health administration.
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Importance of access to epilepsy monitoring units during the COVID-19 pandemic: consensus statement of the International League Against Epilepsy and the International Federation of Clinical Neurophysiology.
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In vivo imaging of epileptic activity using 2-NBDG, a fluorescent deoxyglucose analog.
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Incidence of Poststroke Epilepsy: An Executive Summary.
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Increased AMPA-sensitive quisqualate receptor binding and reduced NMDA receptor binding in epileptic human hippocampus.
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Increased dentate granule cell neurogenesis following amygdala kindling in the adult rat.
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Increased ectopic action potential generation accompanies epileptogenesis in vitro.
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Increased expression of brain-derived neurotrophic factor induces formation of basal dendrites and axonal branching in dentate granule cells in hippocampal explant cultures.
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Induction of epileptiform activity in hippocampal slices by trains of electrical stimuli.
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Influenza vaccination in children with neurologic or neurodevelopmental disorders.
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Initiation, synchronization, and spread of epileptic discharges. Introduction.
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Inter-rater agreement for diagnoses of epilepsy in pregnant women.
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Interactions between sleep and epilepsy.
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Interneuron transplantation: a prospective surgical therapy for medically refractory epilepsy.
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Intractable epilepsy following radiosurgery for arteriovenous malformation.
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Intradentate colchicine retards the development of amygdala kindling.
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Intragenic deletions of ALDH7A1 in pyridoxine-dependent epilepsy caused by Alu-Alu recombination.
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Intranigral dynorphin-1-13 suppresses kindled seizures by a naloxone-insensitive mechanism.
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Intraoperative optical imaging of epileptiform and functional activity.
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Intravenous immunoglobulin therapy in intractable childhood epilepsy: open-label study and review of the literature.
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Introduction to the idiopathic epilepsies.
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Introduction.
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Juvenile acute intermittent porphyria with hypercholesterolemia and epilepsy: a case report and review of the literature.
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Kindling model of epilepsy.
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Letter: Antiepileptogenic and neuroprotective effects of erythropoietin: recent data.
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Leveraging the lessons learned from studies on the cultural context of epilepsy care in Uganda: Opportunities and future directions.
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Limbic epilepsy in transgenic mice carrying a Ca2+/calmodulin-dependent kinase II alpha-subunit mutation.
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Linking hemodynamic and electrophysiological measures of brain activity: evidence from functional MRI and intracranial field potentials.
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Long-Term Potentiation of Mossy Fiber Feedforward Inhibition of CA3 Pyramidal Cells Maintains E/I Balance in Epilepsy Model.
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Longitudinal MRI findings in pyridoxine-dependent seizures.
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Low-grade gliomas associated with intractable epilepsy: seizure outcome utilizing electrocorticography during tumor resection.
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Lysine restricted diet for pyridoxine-dependent epilepsy: first evidence and future trials.
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MRI-guided laser interstitial thermal therapy in an infant with tuberous sclerosis: technical case report.
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Managing the epileptic patient.
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Marked benefits in physical activity and well-being, but not in functioning domains, 2 years after successful epilepsy surgery in children.
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Mechanism of epilepsy.
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Mechanisms of epileptogenesis.
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Mechanisms of increased hippocampal excitability in the Mashl+/- mouse model of Na+ /K+ -ATPase dysfunction.
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Metabolic responses differentiate between interictal, ictal and persistent epileptiform activity in intact, immature hippocampus in vitro.
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Millimeter-scale epileptiform spike patterns and their relationship to seizures.
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Minireview. Kainic acid as a tool for the study of temporal lobe epilepsy.
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Missense Variants in RHOBTB2 Cause a Developmental and Epileptic Encephalopathy in Humans, and Altered Levels Cause Neurological Defects in Drosophila.
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Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy.
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Molecular Genetics and Epilepsy: Foundation for Therapeutic Advances. Proceedings of the 12th annual Merritt-Putnam Symposium. Seattle, Washington, December 5, 1992.
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Mortality in individuals with autism, with and without epilepsy.
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Multicenter Research Data of Epilepsy Management in Patients With Sturge-Weber Syndrome.
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Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study.
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Multiple organ failure after ingestion of pennyroyal oil from herbal tea in two infants.
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Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia.
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NADH fluorescence and [K+]o changes during hippocampal electrical stimulation.
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NMDA antagonists differentiate epileptogenesis from seizure expression in an in vitro model.
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Natural history of pyridoxine-dependent epilepsy: tools for prognostication.
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Neural development, genes and the epilepsies: introduction.
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Neurodevelopmental and Epilepsy Phenotypes in Individuals With Missense Variants in the Voltage-Sensing and Pore Domains of KCNH5.
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Neurofeedback treatment of epilepsy: from basic rationale to practical application.
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Neurologic manifestations of essential thrombocythemia.
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Neuronal ceroid lipofuscinosis diagnosed via skin biopsy.
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Neuronal migration disorders: positron emission tomography correlations.
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Neuropeptide Y in the recurrent mossy fiber pathway.
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New waves of research in the epilepsies: crossing into the third millennium.
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Nocturnal epilepsy in adults.
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Normal adult EEG and patterns of uncertain significance.
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Novel clinical manifestations in patients with KCNA2 mutations.
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Novel therapies for epilepsy in the pipeline.
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Null mutation of c-fos impairs structural and functional plasticities in the kindling model of epilepsy.
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Nutrition: an integral component in the health care of children. The interdisciplinary team in action.
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Nutritional factors and anticonvulsant therapies: effect on growth in children with epilepsy.
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Ontogeny of seizure-induced increases in BDNF immunoreactivity and TrkB receptor activation in rat hippocampus.
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Optical imaging of epileptiform activity in human neocortex.
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Optical imaging of epileptiform and functional activity in human cerebral cortex.
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Optical imaging of visual cortex epileptic foci and propagation pathways.
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Pediatric Sudden Unexpected Death in Epilepsy: What Have we Learned from Animal and Human Studies, and Can we Prevent it?
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Periventricular and subcortical nodular heterotopia. A study of 33 patients.
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Pharmacokinetics of levetiracetam.
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Phenobarbital does not alter phenytoin steady-state serum concentration or pharmacokinetics.
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Phenytoin and phenobarbital concentrations in saliva and plasma measured by radioimmunoassay.
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Physical and Family History Variables Associated With Neurological and Cognitive Development in Sturge-Weber Syndrome.
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Plasticity in the adult human oligodendrocyte lineage.
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Pluralistic and singular causal attributions for epilepsy in Uganda.
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Positron emission tomography in pediatric epilepsy.
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Potassium-induced epileptiform activity in area CA3 varies markedly along the septotemporal axis of the rat hippocampus.
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Potential hepatotoxicity of lamotrigine.
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Predictors of bone density in ambulatory patients on antiepileptic drugs.
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Predictors of outcome of epilepsy surgery: multivariate analysis with validation.
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Preliminary investigation of the use of newborn dried blood spots for screening pyridoxine-dependent epilepsy by LC-MS/MS.
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Principles of drug treatment in children.
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Proceedings of the Second International Workshop on Advances in Electrocorticography.
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Proceedings of the Third International Workshop on Advances in Electrocorticography.
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Progressive neuronal activation accompanies epileptogenesis caused by hippocampal glutamine synthetase inhibition.
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Protein synthesis inhibition blocks maintenance but not induction of epileptogenesis in hippocampal slice.
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Pseudoepileptic seizures: methods and video analysis to aid diagnosis.
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Pseudoseizure manifestations in two preschool age children.
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Pseudoseizures in the military.
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Pseudoseizures: recognition and treatment.
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Pyridoxal phosphate dependency, a newly recognized treatable catastrophic epileptic encephalopathy.
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Pyridoxine dependent epilepsy and antiquitin deficiency: clinical and molecular characteristics and recommendations for diagnosis, treatment and follow-up.
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Pyridoxine-dependent epilepsy and pyridoxine phosphate oxidase deficiency: unique clinical symptoms and non-specific EEG characteristics.
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Pyridoxine-dependent epilepsy: EEG investigations and long-term follow-up.
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Pyridoxine-dependent seizures and cognition in adulthood.
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Rare and common epilepsies converge on a shared gene regulatory network providing opportunities for novel antiepileptic drug discovery.
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Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.
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Rasmussen's encephalitis: an autoimmune disorder?
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Re: Epilepsy-associated bone mineral density loss should be prevented.
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Real-World Preliminary Experience With Responsive Neurostimulation in Pediatric Epilepsy: A Multicenter Retrospective Observational Study.
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Recent advances in understanding mechanisms of the kindling model.
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Reduction of TrkB expression de novo in the adult mouse impairs epileptogenesis in the kindling model.
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Reduction of seizures by transplantation of cortical GABAergic interneuron precursors into Kv1.1 mutant mice.
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Repeatability of quantitative metrics derived from MR diffusion tractography in paediatric patients with epilepsy.
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Repeated seizures induce long-term increase in hippocampal benzodiazepine receptors.
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Responsive stimulation of motor cortex for medically and surgically refractive epilepsy.
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Risk factors for development of subclinical hypothyroidism during valproic acid therapy.
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Robot-guided pediatric stereoelectroencephalography: single-institution experience.
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Role of excitatory pathways in the hippocampal damage produced by kainic acid.
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Role of neurotransmitters in seizure mechanisms in the kindling model of epilepsy.
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Role of the substantia nigra in the kindling model of limbic epilepsy.
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Routine therapeutic monitoring of lamotrigine in epileptic patients using a simple and rapid high performance liquid chromatographic technique.
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Safety of Early Discontinuation of Antiseizure Medication After Acute Symptomatic Neonatal Seizures.
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Seizure Burden, EEG, and Outcome in Neonates With Acute Intracranial Infections: A Prospective Multicenter Cohort Study.
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Seizure activity in vitro: a dual focus model.
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Seizure disorders in mutant mice: relevance to human epilepsies.
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Seizure length and clinical outcome in electroconvulsive therapy using methohexital or thiopental.
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Seizure-like events in brain slices: suppression by interictal activity.
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Seizure-like spreading depression in immature rabbit hippocampus in vitro.
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Seizures and epilepsy after ischemic stroke.
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Seizures down-regulate muscarinic cholinergic receptors in hippocampal formation.
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Self-management of Epilepsy: A Systematic Review.
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Serum sodium levels and related treatment-emergent adverse events during eslicarbazepine acetate use in adults with epilepsy.
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Short-term frequency-dependent plasticity at recurrent mossy fiber synapses of the epileptic brain.
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Significance of Epilepsy & behavior: my personal experience and views.
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Simple high-performance liquid chromatographic method to monitor vigabatrin, and preliminary review of concentrations determined in epileptic patients.
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Sleep disorders in neurology.
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Social impairments in alternating hemiplegia of childhood.
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Sociocultural determinants and patterns of healthcare utilization for epilepsy care in Uganda.
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Solution structure of the NaV1.2 C-terminal EF-hand domain.
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Somatic variants in diverse genes leads to a spectrum of focal cortical malformations.
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Spatiotemporal compression for efficient storage and transmission of high-resolution electrocorticography data.
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Spectrum of neurodevelopmental disease associated with the GNAO1 guanosine triphosphate-binding region.
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Spontaneous rhythmic synchronous activity in epileptic human and normal monkey temporal lobe.
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Spontaneous temporal encephalocele. Case report.
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Stakeholder views of the practical and cultural barriers to epilepsy care in Uganda.
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Stereoelectroencephalography in children: a review.
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Stigma reduction interventions for epilepsy: A systematized literature review.
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Stimulation-induced status epilepticus: role of the hippocampal mossy fibers in the seizures and associated neuropathology.
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Structural plasticity of dentate granule cell mossy fibers during the development of limbic epilepsy.
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Studies of human and monkey "epileptic" neocortex in the in vitro slice preparation.
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Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals.
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Surgical outcome in patients with epilepsy with occult vascular malformations treated with lesionectomy.
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Systemic Manifestations in Pyridox(am)ine 5'-Phosphate Oxidase Deficiency.
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Targeting BDNF/TrkB pathways for preventing or suppressing epilepsy.
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Targeting the Diagnosis in an Adolescent with Epilepsy and Intellectual Disability through Next-Generation Metabolic Screening.
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Technetium-99m HmPAO brain SPECT and outcome of hemispherectomy for intractable seizures.
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Temporal specific patterns of semaphorin gene expression in rat brain after kainic acid-induced status epilepticus.
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The "jerks": mass hysteria or epilepsy?
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The NMDA receptor antagonist 2-amino-5-phosphonovalerate blocks stimulus train-induced epileptogenesis but not epileptiform bursting in the rat hippocampal slice.
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The drug MK-801 attenuates the development, but not the expression, of long-term potentiation and stimulus train-induced bursting in hippocampal slices.
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The effect of vagus nerve stimulation therapy on body mass index in children.
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The effects of baclofen and pertussis toxin on epileptiform activity induced in the hippocampal slice by magnesium depletion.
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The electroencephalogram in pediatric practice: its use and abuse.
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The epileptology of alternating hemiplegia of childhood.
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The future of pediatric epilepsy surgery. Signposts and science.
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The genotypic spectrum of ALDH7A1 mutations resulting in pyridoxine dependent epilepsy: A common epileptic encephalopathy.
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The interictal EEG in diagnosis of epilepsy.
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The ketogenic diet: initiation at goal calories versus gradual caloric advancement.
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The kindling model of epilepsy: a critical review.
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The kindling model of epilepsy: a review.
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The microRNA processor DROSHA is a candidate gene for a severe progressive neurological disorder.
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The microtubule interacting drug candidate NAP protects against kainic acid toxicity in a rat model of epilepsy.
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The neurobiological basis of epilepsy.
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The newer antiepileptic drugs: carbamazepine and valproic acid.
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The preoperative evaluation of the child with epilepsy.
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The role of NMDA receptors in in vitro epileptogenesis.
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The syndrome of aphasia, headaches, and left temporal spikes.
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The tyrosine receptor kinase B ligand, neurotrophin-4, is not required for either epileptogenesis or tyrosine receptor kinase B activation in the kindling model.
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Therapeutic Index Estimation of Antiepileptic Drugs: A Systematic Literature Review Approach.
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Three children with a syndrome of obesity and overgrowth, atypical psychosis, and seizures: a problem in neuropsychopharmacology.
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Three-dimensional brain surface visualization for epilepsy surgery of focal cortical dysplasia.
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Timing of therapy and neurodevelopmental outcomes in 18 families with pyridoxine-dependent epilepsy.
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Topiramate monotherapy as broad-spectrum antiepileptic drug in a naturalistic clinical setting.
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Transcriptional profile of hippocampal dentate granule cells in four rat epilepsy models.
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Tuberous sclerosis complex and epilepsy: prognostic significance of electroencephalography and magnetic resonance imaging.
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Two randomized vitamin D trials in ambulatory patients on anticonvulsants: impact on bone.
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Ultrastructural features and synaptic connections of hilar ectopic granule cells in the rat dentate gyrus are different from those of granule cells in the granule cell layer.
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Understanding the cultural context of epilepsy care in Uganda: Introduction to this special issue.
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Understanding therapeutic equivalence in epilepsy.
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Unsupervised classification of high-frequency oscillations in human neocortical epilepsy and control patients.
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Untargeted metabolomics and infrared ion spectroscopy identify biomarkers for pyridoxine-dependent epilepsy.
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Use of subdural grids and strip electrodes to identify a seizure focus in children.
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Use of vagal nerve stimulation as a treatment for refractory epilepsy in dogs.
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Utility of levetiracetam in patients with subarachnoid hemorrhage.
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Vagal nerve stimulator pocket infections.
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Vagus nerve stimulation in depression.
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Vagus nerve stimulation: a new tool for brain research and therapy.
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Validity of the Personal Impact of Epilepsy Scale (PIES) in patients with epilepsy in Uganda.
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Validity, reliability and cut-offs of the Patient Health Questionnaire-9 as a screening tool for depression among patients living with epilepsy in Rwanda.
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Valproate reduces excitability by blockage of sodium and potassium conductance.
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Video/EEG monitoring in the evaluation of paroxysmal behavioral events: duration, effectiveness, and limitations.
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When do epileptic seizures really begin?
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Working with visual display units.
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X-linked lissencephaly in an Indian family.
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[Systemic manifestations of myasthenia gravis and its putative pathogenesis].
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gamma-Aminobutyric acid and benzodiazepine receptors in the kindling model of epilepsy: a quantitative radiohistochemical study.
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Keywords of People
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Clyde, Merlise,
Professor of Statistical Science,
Statistical Science
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Mandge, Vishal A.,
Assistant Professor of Neurology,
Hospital Neurology
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Muh, Carrie Rebecca,
Adjunct Assistant Professor in the Department of Neurosurgery,
Neurosurgery
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Pitt, Geoffrey Stuart,
Adjunct Professor in the Department of Medicine,
Medicine, Cardiology
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Rada Rincon, Pedro Vicente,
Senior Lecturer in Neuroscience at Duke Kunshan University,
DKU Faculty
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Russ, Jeffrey Brian,
Medical Instructor in the Department of Pediatrics,
Pediatrics, Neurology
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Tchapyjnikov, Dmitry,
Adjunct Assistant Professor in the Department of Pediatrics,
Pediatrics, Neurology
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Zafar, Muhammad Shahzad,
Assistant Professor of Pediatrics,
Pediatrics, Neurology