Results 101 to 110 of about 120,188 (203)

Introducing the D‐DAND scale: Development of a comprehensive caregiver‐administered tool for Dravet syndrome comorbidities

open access: yesEpilepsia, EarlyView.
Graphical overview of the Dravet Disease–Associated Neuropsychiatric Disorders (D‐DAND) scale. The D‐DAND scale provides a caregiver‐based, comprehensive assessment of developmental and behavioral comorbidities in Dravet syndrome across six domains: motor abilities, language and social interaction, autonomies, academic skills, emotional/behavioral ...
Bernardo Dalla Bernardina   +9 more
wiley   +1 more source

Risk Factors for Febrile Seizure Recurrence

open access: yes, 1994
The relation between postulated risk factors and seizure recurrence after a first febrile seizure (FS) was assessed by reanalysis of pooled data from five centers and follow-up studies and reported from the Sophia Children’s Hospital, Rotterdam, The ...
J Gordon Millichap
core   +1 more source

Refining diagnostic boundaries and electroclinical profiles of Lennox–Gastaut syndrome through unsupervised clustering

open access: yesEpilepsia, EarlyView.
Abstract Objective Lennox–Gastaut syndrome (LGS) is a developmental and epileptic encephalopathy defined by polymorphic seizures, intellectual disability (ID), and characteristic electroencephalographic (EEG) patterns. The applicability and biological validity of current electroclinical criteria remain debated.
Emanuele Cerulli Irelli   +12 more
wiley   +1 more source

Febrile Seizure Duration and Development

open access: yes, 2011
Members of the FEBSTAT multicenter Study Team assessed the distribution of febrile seizure (FS) duration in a cohort of 158 children with a first FS, and determined the association between FS duration and behavior and ...
J Gordon Millichap
core   +1 more source

Correlation of polygenic risk score and clinical phenotype in patients with genetic generalized epilepsy

open access: yesEpilepsia, EarlyView.
Abstract Objective The polygenic risk score (PRS) for individuals with genetic generalized epilepsy (GGE) quantifies the common risk variants in genes identified in genome‐wide association studies. We hypothesized that the phenotype of GGE patients differs based on their GGE PRS. Methods We identified participants with highest (n = 59) versus lowest (n 
Sophie von Brauchitsch   +27 more
wiley   +1 more source

The Role of Seizure-Related SEZ6 as a Susceptibility Gene in Febrile Seizures

open access: yesNeurology Research International, 2011
Sixty cases of febrile seizures from a Chinese cohort had previously been reported with a strong association between variants in the seizure-related (SEZ) 6 gene and febrile seizures. They found a striking lack of genetic variation in their controls.
John C. Mulley   +6 more
doaj   +1 more source

Status epilepticus in adults: From etiology to treatment response

open access: yesEpilepsia, EarlyView.
Abstract This study explored the association between etiology of status epilepticus (SE) and treatment responsiveness. Consecutive episodes of nonhypoxic SE in patients ≥14 years old were included. Etiology was classified into acute, remote, progressive, defined electroclinical syndromes, and unknown.
Simona Lattanzi   +5 more
wiley   +1 more source

Gambaran Faktor yang Berhubungan dengan Timbulnya Kejang Demam Berulang pada Pasien yang Berobat di Poliklinik Anak RS. DR. M. Djamil Padang Periode Januari 2010 – Desember 2012

open access: yesJurnal Kesehatan Andalas, 2016
 AbstrakKejang demam merupakan kejang paling sering pada anak yang kemungkinan berulang. Pengetahuan tentang faktor yang berhubungan dengan kejang demam berulang perlu diketahui demi ketepatan tatalaksana.
Vivit Erdina Yunita   +2 more
doaj  

Brain‐wide magnetic resonance imaging analysis of neurobehavioral comorbidities in temporal lobe epilepsy

open access: yesEpilepsia, EarlyView.
Abstract Objective In temporal lobe epilepsy (TLE), patients often present with neurobehavioral comorbidities encompassing affective and cognitive difficulties. Whereas the latter have been related to atypical connectivity of mesiotemporal and frontotemporal circuits, the brain basis of affective symptoms remains incompletely understood.
Fatemeh Fadaie   +4 more
wiley   +1 more source

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