Keywords: آنسفالوپاتی صرعی; Dravet syndrome; SCN1A; myoclonic absence seizures; epileptic encephalopathy; absence seizures;
مقالات ISI ترجمه شده آنسفالوپاتی صرعی
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Keywords: آنسفالوپاتی صرعی; ESES; EEG; Epileptic encephalopathy; Autism; Corticosteroid; Benzodiazepine;
Keywords: آنسفالوپاتی صرعی; EMAS; Doose; Epileptic encephalopathy; Evaluation; Treatment;
Keywords: آنسفالوپاتی صرعی; BOLD; blood oxygen leveldependent; HFO; high frequency oscillation; FCD; focal cortical dysplasia; IEDs; interictal epileptiform discharges; TCI; transient cognitive impairment; EE; epileptic encephalopathy; NCSE; non-convulsive status epilepticus; ELS; e
Keywords: آنسفالوپاتی صرعی; Epileptic encephalopathy; Neuronal auto-antibodies; West syndrome; Lennox-Gastaut syndrome; Immune-mediated epilepsy;
Keywords: آنسفالوپاتی صرعی; KD; Ketogenic diet; AED; Antiepileptic drugs; ILAE; International League against epilepsy; MAE; Myoclonic astatic epilepsy; FIRES; Febrile infection related epileptic syndrome; LGS; Lennox Gastaut syndrome; EE; Epileptic encephalopathy; GLUT 1; Glucose tr
Keywords: آنسفالوپاتی صرعی; AMPA receptor antagonist; Antiepileptic drug; Epilepsy; Epileptic encephalopathy; Lennox-Gastaut syndrome;
Keywords: آنسفالوپاتی صرعی; Myoclono-astatic epilepsy; Doose syndrome; Ketogenic diet; Resistant epilepsy; Epileptic encephalopathy;
Keywords: آنسفالوپاتی صرعی; WDR45; Neurodegeneration with brain iron accumulation; Beta-propeller protein-associated neurodegeneration (BPAN); Epileptic encephalopathy; Brain atrophy; Neuron specific enolase (NSE);
Keywords: آنسفالوپاتی صرعی; Mowat-Wilson syndrome; ESES; Epilepsy; Epileptic encephalopathy; Sleep;
Keywords: آنسفالوپاتی صرعی; diagnostic yield; epilepsy; epileptic encephalopathy; genetic testing;
Keywords: آنسفالوپاتی صرعی; Epileptic encephalopathy; West syndrome; Involuntary movement; Hyperkinetic movement; Hand stereotype; Whole-exome sequencing
Keywords: آنسفالوپاتی صرعی; Ring chromosome 20 syndrome; Age-dependent course; Seizure semiology; Epileptic encephalopathy;
Keywords: آنسفالوپاتی صرعی; Epileptic encephalopathy; Epileptic encephalopathy with continuous spikes and waves during sleep; Infantile spasms; Inflammation; Lennox-Gastaut syndrome;
Keywords: آنسفالوپاتی صرعی; epileptic encephalopathy; infantile spasms; vigabatrin; nontuberous sclerosis complex; efficacy; predictors
Keywords: آنسفالوپاتی صرعی; Epileptic encephalopathy; Ketogenic diet; Steroid; West syndrome; Encephalopathy with CSWS;
Keywords: آنسفالوپاتی صرعی; Epileptic encephalopathy; Ketogenic diet; ESES syndrome; Refractory epilepsy; Seizures;
Keywords: آنسفالوپاتی صرعی; Status epilepticus; Genetics; Cerebral dysplasia; Inborn errors of metabolism; Mitochondrial disease; Epileptic encephalopathy;
Keywords: آنسفالوپاتی صرعی; Epilepsy; Nodding Syndrome; Epileptic encephalopathy; Sub-Saharan Africa; South Sudan; Progressive intellectual disability;
Keywords: آنسفالوپاتی صرعی; Functional neuroimaging techniques; Ring 20 syndrome; Epileptic encephalopathy; EEG-fMRI; PET; SPECT; Behavior;
Keywords: آنسفالوپاتی صرعی; Glutaric aciduria; Maple syrup urine disease; Epileptic encephalopathy; West syndrome
Keywords: آنسفالوپاتی صرعی; Epileptic encephalopathy; Pediatric polysomnography; Sleep-related breathing disorders; Sleep obstructive apnea syndrome; Periodic limb movements
Keywords: آنسفالوپاتی صرعی; Potassium bromide; Epileptic encephalopathy; Focal seizures; Infants; Multifocal seizures; Refractory epilepsy;
Keywords: آنسفالوپاتی صرعی; Antiepileptic drugs; Partial seizures; Epileptic encephalopathy; Pediatrics; Drug resistant epilepsy
Keywords: آنسفالوپاتی صرعی; Rufinamide; Paediatric epilepsy; Lennox–Gastaut syndrome; Epileptic encephalopathy; Focal seizures; Antiepileptic drug interactions
Keywords: آنسفالوپاتی صرعی; AR; autosomal recessive; PDRE; pediatric drug-resistant epilepsy; DRE; drug-resistant epilepsy; EE; epileptic encephalopathy; WES; whole exome sequencing; VUS; variant of unknown significance; AED; antiepileptic drug; IGE; idiopathic generalized epilepsy;
Keywords: آنسفالوپاتی صرعی; Hemimegalencephaly; Hemispherotomy; Developmental outcome; Seizure outcome; Infant; Epileptic encephalopathy;
Keywords: آنسفالوپاتی صرعی; AED; Antiepileptic drug; IGE; Idiopathic generalized epilepsy; ILRE; Idiopathic localization-related epilepsy; LGS; Lennox-Gastaut syndrome; EE; Epileptic encephalopathy; Cognition; Intelligence; Epilepsy; Children; Mental retardation; Seizure;
Keywords: آنسفالوپاتی صرعی; CACNA1A; epilepsy; epileptic encephalopathy; channelopathy; calcium; genetic; lamotrigine
Keywords: آنسفالوپاتی صرعی; HH, hypothalamic hamartoma; EEG-fMRI, EEG with functional MRI; GS, gelastic seizure; SISCOM, SPECT coregistered to MRI; DMN, default mode networkGelastic seizure; Epileptic encephalopathy; Subcortical epilepsy; EEG-fMRI; Ictal SPECT
Keywords: آنسفالوپاتی صرعی; Dravet syndrome; Epileptic encephalopathy; GEFS+; SCN1A mutation
Sulthiame add-on therapy in children with Lennox-Gastaut syndrome: A study of 44 patients
Keywords: آنسفالوپاتی صرعی; Epileptic encephalopathy; Lennox-Gastaut syndrome; Refractory; Sulthiame; Tonic seizures; Drop attacks;
Biallelic mutations in SZT2 cause a discernible clinical entity with epilepsy, developmental delay, macrocephaly and a dysmorphic corpus callosum
Keywords: آنسفالوپاتی صرعی; Intellectual disability; Epileptic encephalopathy; Seizure; Whole-exome sequencing;
Early identification of epileptic encephalopathy with continuous spikes-and-waves during sleep: AÂ case-control study
Keywords: آنسفالوپاتی صرعی; Case-control study; Continuous spikes and waves in sleep; Epileptic encephalopathy; Epilepsy;
Clinical utility of EEG in diagnosing and monitoring epilepsy in adults
Keywords: آنسفالوپاتی صرعی; aEEG; ambulatory electroencephalography; ACNS; American Clinical Neurophysiology Society; ASD; anti-seizure drug; CAA-EEG; computer-assisted aEEG; cEEG; continuous electroencephalography; ECG; electrocardiogram; ECS; electrical cortical stimulation; ECoG;
Case studyUnusual association of SCN2A epileptic encephalopathy with severe cortical dysplasia detected by prenatal MRI
Keywords: آنسفالوپاتی صرعی; Epileptic encephalopathy; Cortical dysplasia; SCN2A; Prenatal diagnosis; Fetal MRI;
Case ReportQuinidine therapy for West syndrome with KCNTI mutation: A case report
Keywords: آنسفالوپاتی صرعی; EOEE; early onset epileptic encephalopathy; MPSI; migrating partial seizures of infancy; LTG; lamotrigine; VPA; valproate; Potassium channel; Epileptic spasms; Epileptic encephalopathy; Treatment; Children;
Case ReportAmelioration of intractable epilepsy by adjunct vagus nerve stimulation therapy in a girl with a CDKL5 mutation
Keywords: آنسفالوپاتی صرعی; Cycling-dependent kinase-like 5; Epileptic encephalopathy; Quality of life; Vagus nerve stimulation therapy;
Case ReportDramatic response after functional hemispherectomy in a patient with epileptic encephalopathy carrying a de novo COL4A1 mutation
Keywords: آنسفالوپاتی صرعی; COL4A1; Epileptic encephalopathy; Hemiplegia; Porencephaly; Infantile spasms; Functional hemispherectomy;
Research PaperAltered gene expression profile in a mouse model of SCN8A encephalopathy
Keywords: آنسفالوپاتی صرعی; RNA-seq; Transcriptome; Seizure; Epileptic encephalopathy; Astrocyte; Gene expression; Sodium channel;
Original articleEpilepsy in patients with GRIN2A alterations: Genetics, neurodevelopment, epileptic phenotype and response to anticonvulsive drugs
Keywords: آنسفالوپاتی صرعی; GRIN2A; Epilepsy; Epileptic encephalopathy; Specialized therapy; ABPE; Atypical Benign Partial Epilepsy of childhood; ACMG; American College of Medical Genetics; AED; antiepileptic drugs; BECTS; benign focal epilepsy with centrotemporal spikes; CLB; cloba
Systemic Manifestations in Pyridox(am)ine 5â²-Phosphate Oxidase Deficiency
Keywords: آنسفالوپاتی صرعی; pyridoxine; epileptic encephalopathy; pyridoxal-5-phosphate; reversible retinopathy;
Severe bone loss and multiple fractures in SCN8A-related epileptic encephalopathy
Keywords: آنسفالوپاتی صرعی; Epileptic encephalopathy; Osteoclast; Neridronate; SCN8A;
Ketogenic diet - A novel treatment for early epileptic encephalopathy due to PIGA deficiency
Keywords: آنسفالوپاتی صرعی; Ketogenic diet; Epileptic encephalopathy; Whole exome sequencing; PIGA;
Case StudySevere early-onset epileptic encephalopathy due to mutations in the KCNA2 gene: Expansion of the genotypic and phenotypic spectrum
Keywords: آنسفالوپاتی صرعی; KCNA2; Epileptic encephalopathy;
A novel PIGA mutation in a family with X-linked, early-onset epileptic encephalopathy
Keywords: آنسفالوپاتی صرعی; PIGA; Epileptic encephalopathy; Focal seizure; Genetics; Infant;
Short communicationAltered GABAA receptor expression in brainstem nuclei and SUDEP in Gabrg2+/Q390X mice associated with epileptic encephalopathy
Keywords: آنسفالوپاتی صرعی; γ2 subunit; Gabrg2+/Q390X knockin (KI) mice; Gabrg2+/â knockout (KO) mice; Epileptic encephalopathy; Brainstem; GABAA receptors; Protein accumulation;
RARS2 mutations cause early onset epileptic encephalopathy without ponto-cerebellar hypoplasia
Keywords: آنسفالوپاتی صرعی; Epileptic encephalopathy; RARS2; Mitochondrial; Pontocerebellar hypoplasia;
Outlining a core neuropsychological phenotype for Dravet syndrome
Keywords: آنسفالوپاتی صرعی; Dravet syndrome; Epileptic encephalopathy; Channelopathy; Neuropsychological phenotypes; Visuoconstructive ability impairment;
Early onset epileptic encephalopathy or genetically determined encephalopathy with early onset epilepsy? Lessons learned from TSC
Keywords: آنسفالوپاتی صرعی; Tuberous sclerosis; Epileptic encephalopathy; Genetics; mTOR; Vigabatrin;