Results 41 to 50 of about 26,425 (290)
Information is Power: An Interventional Study on Parents of Children with Febrile Seizures [PDF]
, 2017 Aim: Febrile seizures (FS) cause great fear and panic in the families. The majority of parents think that they may lose their child during a seizure, and feel anxious about the possibility of seizures recurring in the future.
Deniz Özalp Kızılay +5 more
core +1 more source
Cognitive dysfunction after experimental febrile seizures [PDF]
, 2008 While the majority of children with febrile seizures have an excellent prognosis, a small percentage are later discovered to have cognitive impairment.
Tallie Z. Baram +21 more
core +1 more source
ATP6V0C Is Associated With Febrile Seizures and Epilepsy With Febrile Seizures Plus
Frontiers in Molecular Neuroscience, 2022 PurposeTo identify novel genetic causes of febrile seizures (FS) and epilepsy with febrile seizures plus (EFS+).MethodsWe performed whole-exome sequencing in a cohort of 32 families, in which at least two individuals were affected by FS or EFS+. The probands, their parents, and available family members were recruited to ascertain whether the genetic ...
Yang Tian +22 more
openaire +3 more sources
Have Pandemic Measures Reduced the Frequency of Febrile Seizures? Assessment of the Frequency of Febrile Seizures in the Pre- and Post-COVID-19 Period [PDF]
Introduction: Febrile seizures (FS) are common childhood seizures often triggered by fever. With the emergence of coronavirus disease 2019 (COVID-19), FS cases related to the COVID-19 have also been reported.
Özlem Tolu Kendir +5 more
core +1 more source
Epilepsy‐Associated Variants of a Single SCN1A Codon Exhibit Divergent Functional Properties
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Pathogenic variants in SCN1A, which encodes the voltage‐gated sodium channel NaV1.1, are associated with multiple epilepsy syndromes exhibiting a range of clinical severity. SCN1A variants are reported in different syndromes, including Dravet syndrome, which is associated with loss‐of‐function, whereas neonatal/infantile‐onset ...
Lanie N. Liebovitz +3 more
wiley +1 more source
Multidimensional Profiling of MRI‐Negative Temporal Lobe Epilepsy Uncovers Distinct Phenotypes
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Although hippocampal sclerosis (TLE‐HS) represents the most frequent cause of temporal lobe epilepsy (TLE), up to 30% of patients show no lesion on visual MRI inspection (TLE‐MRIneg). These cases pose diagnostic and therapeutic challenges and are underrepresented in surgical series.
Alice Ballerini +28 more
wiley +1 more source
Avicenna Journal of Medicine, 2020 Background: Febrile seizures are associated with a lot of modifiable and nonmodifiable risk factors. Extensive research is currently going on to discover more and more risk factors of febrile seizures, so that they can be modified to decrease their ...
Jehangir A Bhat +4 more
doaj +1 more source
Elevated Connectivity During Language Processing Is Associated With Cognitive Performance in SeLECTS
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Self‐Limited Epilepsy with Centrotemporal Spikes (SeLECTS) is associated with language impairments despite seizures originating in the motor cortex, suggesting aberrant cross‐network interactions. Here we tested whether functional connectivity in SeLECTS during language tasks predicts language performance.
Wendy Qi +8 more
wiley +1 more source
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Down syndrome regression disorder is a syndrome characterized by subacute loss of cognitive, behavioral, and functional abilities in individuals with Down syndrome. Electroencephalography abnormalities are frequently observed during evaluation, but it remains unclear whether these findings represent a dynamic marker of disease ...
Jonathan D. Santoro +14 more
wiley +1 more source
Neocortex- and hippocampus-specific deletion of Gabrg2 causes temperature-dependent seizures in mice
Cell Death and Disease, 2021 Mutations in the GABRG2 gene encoding the γ-aminobutyric acid (GABA) A receptor gamma 2 subunit are associated with genetic epilepsy with febrile seizures plus, febrile seizures plus, febrile seizures, and other symptoms of epilepsy.
Xinxiao Li +11 more
doaj +1 more source