Search results for "EPILEPSY"

showing 10 items of 420 documents

Excessive Daytime Sleepiness and Sleep Disorders in a Population of Patients with Epilepsy: a Case-Control Study

2016

Background and purpose There are several primary causes for excessive daytime sleepiness (EDS) and sleep disorders in patients with epilepsy. Up to now, studies in the literature report conflicting data in terms of both prevalence and aetiology. The aim of our study was therefore to evaluate the prevalence of EDS and some sleep disorders in a population of patients with epilepsy treated with no more than two antiepileptic drugs (AEDs). We also investigated the role of the depression of mood as a variable that can negatively affect EDS. Methods We prospectively and consecutively recruited 99 patients with a diagnosis of epilepsy, sleep disorders and EDS, belonging to the Centre for Epilepsy …

Pediatricsmedicine.medical_specialtyPopulationExcessive daytime sleepiness03 medical and health sciencesEpilepsy0302 clinical medicineSleep debtObstructive sleep apnoea syndromemedicineRestless legs syndromeGeneralized epilepsyeducationeducation.field_of_studyEpilepsyExcessive daytime sleepinessbusiness.industrySleep disordersmedicine.diseaseMood030228 respiratory systemMood disordersOriginal Articlemedicine.symptombusiness030217 neurology & neurosurgeryJournal of Epilepsy Research
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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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PURA- Related Developmental and Epileptic Encephalopathy: Phenotypic and Genotypic Spectrum

2021

Background and ObjectivesPurine-rich element-binding protein A (PURA) gene encodes Pur-α, a conserved protein essential for normal postnatal brain development. Recently, a PURA syndrome characterized by intellectual disability, hypotonia, epilepsy, and dysmorphic features was suggested. The aim of this study was to define and expand the phenotypic spectrum of PURA syndrome by collecting data, including EEG, from a large cohort of affected patients.MethodsData on unpublished and published cases were collected through the PURA Syndrome Foundation and the literature. Data on clinical, genetic, neuroimaging, and neurophysiologic features were obtained.ResultsA cohort of 142 patients was include…

Pediatricsmedicine.medical_specialtySocio-culturale[SDV.GEN] Life Sciences [q-bio]/GeneticsElectroencephalographyEpilepsyDevelopmental and Epileptic EncephalopathyIntellectual disabilitymedicineGenetics (clinical)feeding difficulties[SDV.GEN]Life Sciences [q-bio]/Geneticsmedicine.diagnostic_testbusiness.industryfungimedicine.diseaseHypotoniaEpileptic spasmsNeonatal hypotonianeonatal hypotoniaEpilepsy syndromesCohortepilepsyNeurology (clinical)medicine.symptombusiness
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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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Ocular Motor Paroxysmal Events in Neonates and Infants: A Review of the Literature

2021

Abstract Background Ocular paroxysmal events can accompany a variety of neurological disorders. Particularly in infants, ocular paroxysmal events often represent a diagnostic challenge. Distinguishing between epileptic and nonepileptic events or between physiological and pathologic paroxysmal events can be challenging at this age because the clinical evaluation and physical examination are often limited. Continuous polygraphic video-electroencephalography (EEG) monitoring can be helpful in these situations. Methods We review ocular paroxysmal events in newborns and infants. The aim is to improve clinical recognition of ocular paroxysmal events and provide a guide to further management. Usin…

Pediatricsmedicine.medical_specialtygenetic structuresOcular motorSocio-culturaleEpileptic phenomenaPhysical examinationNystagmusElectroencephalographyOpsoclonus.NystagmuDiagnosis DifferentialNystagmus03 medical and health sciencesEpileptic phenomena; Newborn; Nonepileptic phenomena; Nystagmus; Opsoclonus0302 clinical medicineOcular Motility DisordersDevelopmental NeuroscienceNeuroimaging030225 pediatricsmedicineHumansNonepileptic phenomenaEpilepsymedicine.diagnostic_testbusiness.industryInfant NewbornInfantMultimodal therapyElectroencephalographyOpsoclonusNewborneye diseasesNeurologyPediatrics Perinatology and Child HealthEtiologyNeurology (clinical)medicine.symptombusinessClinical evaluation030217 neurology & neurosurgery
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Motor and cognitive functions in newly diagnosed adult seizure patients before antiepileptic medication

2000

Objective– Motor and cognitive functions in patients with partial or generalized onset of seizures were evaluated prior to the adminstration of antiepileptic medication. Material and methods– Motor function, attention and memory of 52 consecutive newly diagnosed adult patients with partial or generalized seizures were assessed with neuropsychological tests. Results– Patients with partial onset of seizures did not differ from patients with generalized seizures in tests of motor function or attention, nor in tests of learning and memory. Compared to controls patients with epilepsy performed significantly worse on visual motor tasks, mental flexibily and in delayed visual memory. Within the pa…

Pediatricsmedicine.medical_specialtymedicine.diagnostic_testMemoriaCognitive flexibilityNeuropsychologyPoison controlCognitionGeneral MedicineNeuropsychological testmedicine.diseaseEpilepsyNeurologyVisual memorymedicineNeurology (clinical)PsychiatryPsychologyActa Neurologica Scandinavica
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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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Corrigendum to “Antiabsence effects of carbenoxolone in two genetic animal models of absence epilepsy (WAG/Rij rats and lh/lh mice)”

2009

Corrigendum to ‘‘Antiabsence effects of carbenoxolone in two genetic animal models of absence epilepsy (WAG/Rij rats and lh/lh mice)’’ Pietro Gareri , Daniele Condorelli , Natale Belluardo , Rita Citraro , Vincenza Barresi , Angela Trovato-Salinaro , Giuseppa Mudo‘ , Guido Ferreri Ibbadu , Emilio Russo , Giovambattista De Sarro a,* a Section of Pharmacology, Department of Experimental and Clinical Medicine, Faculty of Medicine and Surgery, University of Catanzaro, Catanzaro, Italy b Section of Biochemistry and Molecular Biology, Department of Chemical Sciences, University of Catania, Catania, Italy Department of Experimental Medicine, University of Palermo, Palermo, Italy

PharmacologyCellular and Molecular NeuroscienceEpilepsymedicineCarbenoxolonePharmacologyPsychologymedicine.diseasemedicine.drugNeuropharmacology
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Nigral control of hippocampal epilepsy: a dopaminergic hypothesis

1988

PharmacologyEpilepsybusiness.industryDopamineDopaminergicHippocampusSubstantia nigraHippocampal formationmedicine.diseaseHippocampusBasal GangliaElectric StimulationSubstantia NigraKineticsEpilepsyDopamineBasal gangliaCatsHaloperidolmedicineAnimalsHaloperidolbusinessNeurosciencemedicine.drugPharmacological Research Communications
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Neurotransmitters involved in the habenular control of raphe-hippocampal circuit

1989

PharmacologyNeurotransmitter AgentsEpilepsyRapheChemistryHippocampusHippocampal formationHippocampusElectric StimulationCochleaHabenulaNeural PathwaysCatsAnimalsRaphe NucleiSerotoninNeuroscienceLateral habenula5-HT receptorPharmacological Research
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