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Refractory Seizures sentence examples within levetiracetam phenytoin sodium



DRESS complicated by Haemophagocytic lymphohistiocytosis. Is screening required?



Antiepileptic drugs


Refractory Seizures sentence examples within Onset Refractory Seizures



Cerebral folate transporter deficiency: a potentially treatable neurometabolic disorder.



Epileptic encephalopathy caused by ARV1 deficiency: Refinement of the genotype–phenotype spectrum and functional impact on GPI‐anchored proteins


Refractory Seizures sentence examples within Medically Refractory Seizures



Socio-economic impact on epilepsy outside of the nation-wide COVID-19 pandemic area



Ketogenic Diet in Infants with Early-Onset Epileptic Encephalopathy and SCN2A Mutation




Refractory Seizures sentence examples within Developed Refractory Seizures



DRESS complicated by Haemophagocytic lymphohistiocytosis. Is screening required?



Drug rash with eosinophilia and systemic symptoms complicated by haemophagocytic lymphohistiocytosis: is screening required?


Refractory Seizures sentence examples within Treat Refractory Seizures



Vagal nerve stimulation : less explored entity in surgical patients!



A Comprehensive Review of Cannabis in Patients with Cancer: Availability in the USA, General Efficacy, and Safety


Refractory Seizures sentence examples within Included Refractory Seizures



Neuronal Ceroid Lipofuscinoses in Children



Hashimoto’s encephalopathy in children: different manifestations of five cases


Refractory Seizures sentence examples within Worsening Refractory Seizures



Child Neurology: Late-Onset Vitamin B6–Dependent Epilepsy Identified by Rapid Genome Sequencing



Absent Words, Present Person


Refractory Seizures sentence examples within refractory seizures starting



Developmental and epileptic encephalopathies: Is prognosis related to different epileptic network dysfunctions?



Child Neurology: Late-Onset Vitamin B6–Dependent Epilepsy Identified by Rapid Genome Sequencing


Refractory Seizures sentence examples within refractory seizures associated



Cannabidiol Therapy for Refractory Epilepsy and Seizure Disorders.



Successful implementation of classical ketogenic dietary therapy in a patient with Niemann-Pick disease type C


Refractory Seizures sentence examples within refractory seizures followed



Epileptic encephalopathy caused by ARV1 deficiency: Refinement of the genotype–phenotype spectrum and functional impact on GPI‐anchored proteins



Homozygous SCN1B variants causing early infantile epileptic encephalopathy 52 affect voltage‐gated sodium channel function


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10.1007/s00381-021-05218-4

Everolimus as a possible prenatal treatment of in utero diagnosed subependymal lesions in tuberous sclerosis complex: a case report



Adjunctive everolimus therapy for tuberous sclerosis complex-associated refractory seizures: Results from the postextension phase of EXIST-3.


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10.1016/j.braindev.2021.02.002

Ketogenic diet for refractory epilepsy with MEHMO syndrome: Caution for acute necrotizing pancreatitis


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10.1177/00034894211047459

Intermittent Vagal Nerve Stimulation-Associated Vocal Fold Movement Impairment.



Is fundoplication mandatory in children with neurological impairment undergoing gastrostomy?



Hemimegalencephaly and intractable seizures associated with the NPRL3 gene variant in a newborn: A case report


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10.3389/fneur.2021.640371

Metabolic Seizures


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10.1016/j.yebeh.2020.107654

Developmental and epileptic encephalopathies: Is prognosis related to different epileptic network dysfunctions?



Intimal cardiac sarcoma in an adolescent presenting with sudden cardiogenic shock


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10.3389/fncel.2021.751762

Sharp-Wave Ripple Frequency and Interictal Epileptic Discharges Increase in Tandem During Thermal Induction of Seizures in a Mouse Model of Genetic Epilepsy


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10.1007/s40263-020-00784-8

Expanding the Treatment Landscape for Lennox-Gastaut Syndrome: Current and Future Strategies



ATP1A1 de novo Mutation-Related Disorders: Clinical and Genetic Features


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10.1016/j.neulet.2021.135800

Effects of antiepileptic drugs on hormones


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10.1016/S2352-3026(21)00136-8

Severe toxicity free survival: physician-derived definitions of unacceptable long-term toxicities following acute lymphocytic leukaemia.



Precision therapy in the genetic epilepsies of childhood



Combined use of emapalumab and ruxolitinib in a patient with refractory hemophagocytic lymphohistiocytosis was safe and effective


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10.1016/J.INAT.2021.101094

Perampanel in cases of refractory temporal lobe epilepsy – A report of two post-operative and two eligible for temporal lobectomy



Chapeau de gendarme in a toddler points to focal epilepsy originating from the subcentral gyrus.


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10.3390/biomedicines9040425

Inhibition of AKT/GSK3β/CREB Pathway Improves the Responsiveness to AMPA Receptor Antagonists by Regulating GRIA1 Surface Expression in Chronic Epilepsy Rats



Brain vessel segmentation in contrast-enhanced T1-weighted MR Images for deep brain stimulation of the anterior thalamus using a deep convolutional neural network



A Systematic Review and Meta-Analysis of Immunoglobulin G Abnormalities and the Therapeutic Use of Intravenous Immunoglobulins (IVIG) in Autism Spectrum Disorder


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10.3390/biomedicines9081069

AMPA Receptor Antagonists Facilitate NEDD4-2-Mediated GRIA1 Ubiquitination by Regulating PP2B-ERK1/2-SGK1 Pathway in Chronic Epilepsy Rats


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10.1016/j.cegh.2021.100827

A cross-sectional study on COVID19 mortality among people below 30 years of age in Tamilnadu-2020



Is STN Neuromodulation of Focal Motor Seizures Ready for Prime Time?


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10.1016/j.yebeh.2020.107713

Genetic pathogenesis of the epileptogenic lesions in Tuberous Sclerosis Complex: Therapeutic targeting of the mTOR pathway



Atypical Presentation of Cerebral Palsy and Seizures: A Case Report on Rasmussen’s Encephalitis in an Adolescent


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10.1007/978-3-030-57369-0_7

Cannabidiol Therapy for Refractory Epilepsy and Seizure Disorders.



Case Report of 3-Phosphoglycerate Dehydrogenase Deficiency: A Baby with Severe Microcephaly, Psychomotor Delay, and Seizures


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10.1016/j.scr.2021.102224

Establishment of an induced pluripotent stem cell line (ZJSHi001-A) from a patient with epileptic encephalopathy carrying KCNB1 Glu330Asp mutation.


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10.1523/ENEURO.0024-21.2021

Loss of KCNQ2 or KCNQ3 Leads to Multifocal Time-Varying Activity in the Neonatal Forebrain Ex Vivo


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10.1136/bmjno-2021-000144

Safety and efficacy of lacosamide versus phenytoin for refractory seizures in neurosurgical patients


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10.2174/1386207324666210219103430

Status analysis of herbal drug therapies in epilepsy: advancements in the use of medicinal plants with anti-inflammatory properties.



Seizure Outcome after Lesionectomy With or Without Concomitant Anteromedial Temporal Lobectomy for Low-Grade Gliomas of the Medial Temporal Lobe


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10.1016/j.eplepsyres.2021.106562

Lateralizing magnetic resonance imaging findings in mesial temporal sclerosis and correlation with seizure and neurocognitive outcome after temporal lobectomy


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10.1016/j.ymgmr.2021.100723

Successful implementation of classical ketogenic dietary therapy in a patient with Niemann-Pick disease type C


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10.1080/13696998.2021.1887877

Modeling the Economic Value of Ceribell Rapid Response EEG in the Inpatient Hospital Setting.


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10.22541/AU.161142051.19089910/V1

Role of Permeability glycoprotein (P-gp) and Multidrug resistance protein 1 (MRP-1) in drug-resistance in mesial temporal lobe epilepsy


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10.1007/s40278-021-03488-x

Multiple drugs


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10.1016/j.ejpn.2021.05.016

Facilitation of drug-resistant epilepsy and catastrophic status epilepticus in children with combined pituitary hormone deficiency.


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10.1136/jmedgenet-2021-107769

Loss-of-function variants in DNM1 cause a specific form of developmental and epileptic encephalopathy only in biallelic state



Treatable Cause of Refractory Seizures in an Infant with a Novel Mutation


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10.1016/j.jep.2021.114338

Pergularia daemia hydro-ethanolic extract protects against pentylenetetrazole kindling-induced seizures, oxidative stress, and neuroinflammation in mice.


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10.1016/j.nbd.2021.105329

Early 17β-estradiol treatment reduces seizures but not abnormal behaviour in mice with expanded polyalanine tracts in the Aristaless related homeobox gene (ARX)



Novel Concepts for the Role of Chloride Cotransporters in Refractory Seizures


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10.30834/kjp.34.1.2021.269

Subcortical band heterotopia and pachygyria with cognitive deterioration in an elderly patient


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10.3389/fgene.2021.644447

Analysis of the Phenotypic Variability as Well as Impact of Early Diagnosis and Treatment in Six Affected Families With ALDH7A1 Deficiency


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10.1016/j.yebeh.2021.107774

Surgical targeting of large hypothalamic hamartomas and seizure-freedom following MR-guided laser interstitial thermal therapy


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10.1007/s13311-020-01000-7

Revisiting Brain Tuberous Sclerosis Complex in Rat and Human: Shared Molecular and Cellular Pathology Leads to Distinct Neurophysiological and Behavioral Phenotypes



A study on etiology, clinical profile and outcome of acute febrile encephalopathy in children: A prospective study at a tertiary care center of Eastern India



Dyke–Davidoff–Masson Syndrome: A Rare Cause of Acquired Cerebral Hemiatrophy


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10.4103/jpgm.JPGM_1165_20

Unusual presentation of an insulinoma in an elderly male patient


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10.3389/fneur.2021.690847

Multidimensional Approach Assessing the Role of Interleukin 1 Beta in Mesial Temporal Lobe Epilepsy


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10.1136/postgradmedj-2021-140396

Claustrum hyperintensity as a marker of anti-NMDAR encephalitis



Acute febrile encephalopathy and seizures in children with diffusion restriction lesions on magnetic resonance imaging brain: A case series


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10.1007/s10072-021-05367-z

Epilepsia partialis continua as the presenting feature of anti-NMDA receptor encephalitis in a young male



Refractory Seizure in a Patient With Griscelli Syndrome: A Unique Case With One Mutation and a Novel Deletion


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