Results 51 to 60 of about 106,832 (306)
Etiology of epilepsy a prospective study of 210 cases
Arquivos de Neuro-Psiquiatria, 1991 The objective of this study was to establish the etiology of epilepsy in 210 chronic epileptics (110 female, 100 male), aged 14-82 years (34.2±13.3). Patients less than 10 years-old and alcoholism were excluded.
Walter Oleschko Arruda
doaj +1 more source
Everolimus dosing recommendations for tuberous sclerosis complex–associated refractory seizures [PDF]
, 2018 ObjectiveThe present analysis examined the exposure-response relationship by means of the predose everolimus concentration (C-min) and the seizure response in patients with tuberous sclerosis complex-associated seizures in the EXIST-3 study ...
Brandt, Christian +12 more
core +2 more sources
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Super‐Refractory Status Epilepticus (SRSE) is a rare, life‐threatening neurological emergency with unclear etiology in many cases. Mitochondrial dysfunction, often due to disease‐causing genetic variants, is increasingly recognized as a cause, with each gene producing distinct pathophysiological mechanisms.
Pouria Mohammadi +2 more
wiley +1 more source
Long⁃term management of intractable epilepsy in children
Chinese Journal of Contemporary Neurology and Neurosurgery, 2012 Achievement of seizure free is the ultimate goal of patients with epilepsy. Lifelong treatment may be needed in some epileptic children, especially in those with intractable epilepsy.
Yu⁃jie LIU, Li⁃ping ZOU
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Developmental and Epileptic Encephalopathy due to Biallelic Pathogenic Variants in PIGM
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective PIGM encodes a critical enzyme in the glycosylphosphatidylinositol (GPI)‐anchor biosynthesis pathway. While promoter‐region mutations in PIGM have been associated with a relatively mild phenotype characterized by portal vein thrombosis and absence seizures, recent evidence suggests that coding‐region mutations result in a more severe
Júlia Sala‐Coromina +11 more
wiley +1 more source
Audit of 100 cases of Epilepsy in a Tertiary Care Hospital
Gomal Journal of Medical Sciences, 2010 Background: Epilepsy is not an uncommon disease. Around 50 million people worldwide have epilepsy. The objective of this study was to evaluate the frequency and causes of epilepsy in our set up.
Nowshad Khan +3 more
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Structural imaging biomarkers of sudden unexpected death in epilepsy. [PDF]
, 2015 Sudden unexpected death in epilepsy is a major cause of premature death in people with epilepsy. We aimed to assess whether structural changes potentially attributable to sudden death pathogenesis were present on magnetic resonance imaging in people who ...
Balestrini, Simona +12 more
core +3 more sources
Ketogenic Diet as an Epigenetic Therapy in SETD1B‐Related Epilepsy
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Histone lysine methyltransferases such as SETD1B regulate chromatin structure and gene transcription. Ketone bodies, including butyrate, act as histone deacetylase inhibitors. We report a 4‐year‐old boy with SETD1B‐related absence epilepsy, refractory to conventional medications, who achieved sustained > 90% seizure reduction on the Modified ...
Erica Tsang +10 more
wiley +1 more source
Attention Deficits, ADHD, and Complex Partial Seizures
Pediatric Neurology Briefs, 1999 The degree of attention deficits in children with complex partial seizures (CPS), with and without ADHD, were compared with that found in children with ADHD but without epilepsy, in a study at the Department of Educational Psychology, University of Texas,
J Gordon Millichap
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Multiscale Information Decomposition: Exact Computation for Multivariate Gaussian Processes [PDF]
, 2017 Exploiting the theory of state space models, we derive the exact expressions of the information transfer, as well as redundant and synergistic transfer, for coupled Gaussian processes observed at multiple temporal scales.
Faes, Luca +2 more
core +3 more sources