Search results for "Seizure"

showing 10 items of 203 documents

Symptomatic seizures in preterm newborns: A review on clinical features and prognosis

2018

Abstract Neonatal seizures are the most common neurological event in newborns, showing higher prevalence in preterm than in full-term infants. In the majority of cases they represent acute symptomatic phenomena, the main etiologies being intraventricular haemorrhage, hypoxic-ischemic encephalopathy, central nervous system infections and transient metabolic derangements. Current definition of neonatal seizures requires detection of paroxysmal EEG-changes, and in preterm newborns the incidence of electrographic-only seizures seems to be particularly high, further stressing the crucial role of electroencephalogram monitoring in this population. Imaging work-up includes an integration of serial…

Pediatricsmedicine.medical_specialtyPrognosiDevelopmental DisabilitiesPopulationEncephalopathyInfant Premature DiseasesReviewElectroencephalographyCerebral palsy03 medical and health sciencesEpilepsy0302 clinical medicineRisk FactorsSeizures030225 pediatricsmedicineNewborn; Outcome; Prognosis; Seizures; TreatmentHumanseducationNeurophysiological MonitoringUltrasonographyOutcomeeducation.field_of_studymedicine.diagnostic_testbusiness.industryInfant Newbornlcsh:RJ1-570BrainSymptomatic seizuresElectroencephalographylcsh:PediatricsGeneral MedicineOff-Label Usemedicine.diseaseNewbornPrognosisMagnetic Resonance ImagingNeurophysiological MonitoringSeizureTreatmentEtiologyAnticonvulsantsbusiness030217 neurology & neurosurgeryInfant Premature
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Febrile seizure and related syndromes

2018

Abstract Febrile seizures (FS) are the result of particular sensitivity to fever in the developing brain, have a major genetic predisposition, and nearly always have a benign outcome. Febrile seizures are the most common for of seizures in childhood. They have been observed in 2–6% of children before the age of 5 years, but in some populations this figure increase to 15%. Febrile seizures could be the first manifestations of epilepsy. About 13% of epileptic patients have a history of febrile seizures, and 30% have had recurrent febrile seizures Their phenotypic characteristics allow, in the majority of cases, a classification of the seizure, an elaboration of a prognosis and to assume a spe…

Pediatricsmedicine.medical_specialtybusiness.industryGeneral Neurosciencemedicine.disease03 medical and health sciencesPsychiatry and Mental healthEpilepsy0302 clinical medicineDravet syndrome030225 pediatricsAnesthesiaFebrile seizureEpilepsy syndromesGenetic predispositionMedicineMultifactorial InheritanceNeurology (clinical)Risk factorbusiness030217 neurology & neurosurgeryMedical literatureNeurology, Psychiatry and Brain Research
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The effect of cannabinoid receptor agonist WIN 55,212-2 on anxiety-like behavior and locomotion in a genetic model of absence seizures in the elevate…

2022

GAERS and NEC rats were treated with cannabinoid 1/2 receptor agonist WIN 55,212-2 2 mg/kg and tested on the Elevated Plus-Maze

PharmacologyCannabinoid Receptor AgonistsModels GeneticMorpholinesNECWIN 55212-2 2AnxietyNaphthalenesSettore BIO/09 - FisiologiaBenzoxazinesRatsElevated Plus Maze TestPsychiatry and Mental healthEpilepsy AbsenceSeizuresPhysiology (medical)GAERSAnimalsPharmacology (medical)Elevated Plus-MazeRats WistarLocomotionCNS neurosciencetherapeutics
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The control of amygdaloid and temporal paroxysmal activity by the caudate nucleus

1971

In gatti curarizzati ed in gatti portatori di elettrodi a dimora e liberi di muoversi, la stimolazione ripetitiva ad alta frequenza del nucleo caudato inibisce la comparsa sia dei fenomeni bioelettrici parossistici focalizzati nell'amigdala e nella corteccia temporale sia dei fenomeni comportamentali omologabili all'epilessia psicomotoria.

Pharmacologymedicine.medical_specialtyCaudate nucleusCell BiologyBiologyAmygdalaElectric StimulationTemporal LobeCellular and Molecular NeuroscienceEndocrinologyEpilepsy Temporal LobeSeizuresAnesthesiaInternal medicineCatsmedicineAnimalsMolecular MedicineCaudate NucleusMolecular BiologyExperientia
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Influence of carbenoxolone on the anticonvulsant efficacy of conventional antiepileptic drugs against audiogenic seizures in DBA/2 mice

2004

Carbenoxolone, the succinyl ester of glycyrrhetinic acid, is an inhibitor of 11beta-hydroxy steroid dehydrogenase and gap junctional intercellular communication. It is currently used in clinical treatment of ulcer diseases. Systemic administration of carbenoxolone (1-40 mg/kg, intraperitoneally (i.p.)) was able to produce a dose-dependent decrease in DBA/2 audiogenic seizure severity score. Glycyrrhizin, an analogue of carbenoxolone inactive at the gap-junction level, was unable to affect audiogenic seizures at doses up to 30 mg/kg. In combination with conventional antiepileptic drugs, carbenoxolone, 0.5 mg/kg, i.p., which per se did not significantly affect the occurrence of audiogenic sei…

PhenytoinAudiogenic seizureGap junctionmedicine.medical_treatmentCarbenoxoloneMotor ActivityLamotriginePharmacologyEpilepsy ReflexFelbamateMicemedicineAnimalsAnticonvulsant potencyPharmacologyValproateEpilepsybusiness.industryDrug SynergismCarbamazepineFelbamateCarbamazepineAnticonvulsantAcoustic StimulationMice Inbred DBAPhenytoinDBA/2CarbenoxoloneAnticonvulsantsPhenobarbitalbusinessDiazepamAntiepileptic drugmedicine.drug
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Antiepileptic drug use in nursing home residents: a cross-sectional, regional study.

2006

Summary The use of antiepileptic drugs (AED), their primary indication, comorbid conditions, and concomitant medications were collected from 565 nursing homes (NH) residents of six NH located around the city of Mainz, Germany representing 5.05% of all NH residents in the area. Data were collected from the electronic pharmacy files and by reviewing all available medical records. Average age was 82.2±2.4 years, 85.5% were women. Of 565 NH residents 28 (4.96%) received AED therapy, of which in 17 (63%) AED were prescribed for a seizure-related diagnosis. In 76.5% seizure types were unspecified and a distinction in focal and generalized epilepsy was made in only 23.5% of patients. Three patient…

PhenytoinMalemedicine.medical_specialtyClinical NeurologyPharmacyEpilepsyDrug Utilization ReviewGermanyHealth caremedicineHomes for the AgedHumansGeneralized epilepsyAgedAged 80 and overEpilepsybusiness.industrySeizure typesMedical recordPharmacoepidemiologyGeneral MedicineCarbamazepinemedicine.diseaseNursing HomesCross-Sectional StudiesNeurologyEmergency medicineAnticonvulsantsFemaleNeurology (clinical)Medical emergencybusinessmedicine.drugSeizure
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TRESK channel contributes to depolarization-induced shunting inhibition and modulates epileptic seizures.

2020

Glutamatergic and GABAergic synaptic transmission controls excitation and inhibition of postsynaptic neurons, whereas activity of ion channels modulates neuronal intrinsic excitability. However, it is unclear how excessive neuronal excitation affects intrinsic inhibition to regain homeostatic stability under physiological or pathophysiological conditions. Here, we report that a seizure-like sustained depolarization can induce short-term inhibition of hippocampal CA3 neurons via a mechanism of membrane shunting. This depolarization-induced shunting inhibition (DShI) mediates a non-synaptic, but neuronal intrinsic, short-term plasticity that is able to suppress action potential generation and…

Potassium ChannelsAction PotentialsNeurotransmissionLigandsGeneral Biochemistry Genetics and Molecular BiologyIon ChannelsEpilepsyGlutamatergicPostsynaptic potentialSeizuresmedicinePotassium Channel BlockersAnimalsHumansRNA MessengerIon channelgamma-Aminobutyric AcidMice KnockoutNeuronsChemistryDepolarizationmedicine.diseaseMice Inbred C57BLHEK293 CellsGene Expression RegulationSynapsesCalciumNeuroscienceShunting inhibitionIonotropic effectCell reports
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Linkage analysis and disease models in benign familial infantile seizures: a study of 16 families.

2006

Summary: Purpose: Benign familial infantile seizures (BFIS) is a genetically heterogeneous condition characterized by partial seizures, onset age from 3 to 9 months, and favorable outcome. BFIS loci were identified on chromosomes 19q12-13.1 and 16p12-q12, allelic to infantile convulsions and choreathetosis. The identification of SCN2A mutations in families with only infantile seizures indicated that BFNIS and BFIS may show overlapping clinical features. Infantile seizures also were in a family with familial hemiplegic migraine and mutations in the ATP1A2 gene. We have examined the heterogeneous genetics of BFIS by means of linkage analysis. Methods: Sixteen families were examined. Probands …

ProbandMaleGenetic LinkagePenetranceEpilepsyModelsgeneticsTomographyFamilial hemiplegic migraineGeneticsNeurologic ExaminationBrainChromosome MappingElectroencephalographyPenetranceMagnetic Resonance Imagingstatistics /&/ numerical dataPedigreeX-Ray ComputedNeurologyFemaleHumanmedicine.medical_specialtyBenign NeonatalBrain; pathology/radiography Chromosome Mapping Chromosomes; Human; Pair 16; genetics Chromosomes; Pair 19; genetics Electroencephalography; statistics /&/ numerical data Epilepsy; Benign Neonatal; diagnosis/genetics Family Female Genetic Heterogeneity Genetic Linkage Haplotypes Humans Magnetic Resonance Imaging Male Models; Genetic Mutation; genetics Neurologic Examination Pedigree Penetrance Tomography; X-Ray Computedpathology/radiographyChromosomesGenetic HeterogeneityGeneticGenetic linkageFebrile seizureGenetic modelmedicineHumansFamilyPsychiatryEpilepsyModels GeneticPair 19Genetic heterogeneitybusiness.industryPair 16medicine.diseaseEpilepsy Benign NeonatalHaplotypesMutationNeurology (clinical)Tomography X-Ray ComputedbusinessChromosomes Human Pair 19Chromosomes Human Pair 16diagnosis/genetics
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NEUROPHYSIOLOGICAL AND NEUROCHEMICAL STUDIES WITH THE ISONICOTINOYLHYDRAZONE OF PYRIDOXAL 5-PHOSPHATE.

1964

Pyridoxal 5-PhosphateBrain chemistryCarboxy-LyasesBiochemistryCellular and Molecular Neurosciencechemistry.chemical_compoundNeurochemicalMesencephalonSeizuresCerebellumPonsIsoniazidPyridoxal phosphateTransaminasesBrain ChemistryPharmacologyMedulla OblongataGallamine TriethiodideChemistryAminobutyratesResearchBrainFrontal LobeElectrophysiologyBiochemistryPyridoxal PhosphateCatsJournal of neurochemistry
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Doege-Potter syndrome: When seizures and hypoglycemia collide.

2018

Reactive HypoglycemiaSeizuresInsulin-Like Growth FactorsElectroencephalographySolitary Fibrous Tumor of the PleuraLetter to EditorHypoglycemiaIranian journal of neurology
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