Results 61 to 70 of about 24,154 (255)
Epilepsia, EarlyView.Abstract Objective Adults with epilepsy and intellectual disabilities (IDs) may be at increased risk of dementia, but clinical evaluation is complex and use of conventional biomarkers is often considered too invasive. We explored abnormality of serum neurofilament light chain (NfL), glial fibrillary acidic protein (GFAP), and phosphorylated tau‐217 (p ...
Hadassa Kwetsie +10 more
wiley +1 more source
Case Reports in Neurological Medicine, 2015 Inherited channelopathies are a heterogeneous group of disorders resulting from dysfunction of ion channels in cellular membranes. They may manifest as diseases affecting skeletal muscle contraction, the conduction system of the heart, nervous system ...
Muthiah Subramanian +2 more
doaj +1 more source
Gastaut type idiopathic occipital epilepsy
Неврология, нейропсихиатрия, психосоматика, 2015 Idiopathic occipital epilepsy is a rare epileptic syndrome. Its incidence in a Novosibirsk cohort of patients with idiopathic focal epilepsy is 0.9%. Objective: to present a clinical description of new cases of Gastaut syndrome, the types of its course ...
I. V. Volkov, O. K. Volkova
doaj +1 more source
Clinical reasoning in feline epilepsy: Which combination of clinical information is useful? [PDF]
, 2017 We sought to identify the association between clinical risk factors and the diagnosis of idiopathic epilepsy (IE) or structural epilepsy (SE) in cats, using statistical models to identify combinations of discrete parameters from the patient signalment ...
Packer, R M A +4 more
core +2 more sources
Epilepsia, EarlyView.Overview of the multimodal experimental approach integrating clinical, genetic, in silico, and in vitro investigations. Clinical: Representative EEG recording setup and ictal traces from affected patients. Genetic: Pedigrees for Families A and B highlighting the inheritance of the four identified SLC12A5 variants (A1, A2, B1, B2).
Mira Hamze +19 more
wiley +1 more source
Epilepsy syndromes classification
Epilepsia Open, EarlyView.Abstract Epilepsy syndromes are distinct electroclinical entities which have been recently defined by the International League Against Epilepsy Nosology and Definitions Task Force. Each syndrome is associated with “a characteristic cluster of clinical and EEG features, often supported by specific etiologic findings”.
Elaine C. Wirrell +4 more
wiley +1 more source
Localization of Generalized Spike and Wave Discharge and Valproate Response
Pediatric Neurology Briefs, 2013 Investigators at Universities of Cincinnati, OH, and Birmingham, Alabama; and Montreal Neurological Institute, Canada, studied the EEG and functional magnetic resonance imaging (fMRI) in 89 patients with idiopathic generalized epilepsy (IGE), (25 with ...
J Gordon Millichap
doaj +1 more source
Pathogenic Cav3.2 channel mutation in a child with primary generalized epilepsy. [PDF]
, 2019 Two paternally-inherited missense variants in CACNA1H were identified and characterized in a 6-year-old child with generalized epilepsy. Febrile and unprovoked seizures were present in this child.
Gandini, Maria A +7 more
core +3 more sources
Seizure Aggravation in Idiopathic Generalized Epilepsies [PDF]
Epilepsia, 2005 Summary: Seizures in the idiopathic generalized epilepsies (IGEs) usually remit completely with antiepileptic drugs (AEDs). Occasionally, however, they may be aggravated by AEDs. Before attributing exacerbation of seizures to an AED, alternative explanations need to be excluded.
J, Chaves, J W, Sander
openaire +2 more sources
Epilepsia Open, EarlyView.Abstract The intestinal microbiome plays a pivotal role in maintaining host health through its involvement in gastrointestinal, immune, and central nervous system (CNS) functions. Recent evidence underscores the bidirectional communication between the microbiota, the gut, and the brain and the impact of this axis on neurological diseases, including ...
Teresa Ravizza +4 more
wiley +1 more source