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441
Relationship between Zinc (Zn2+) and Glutamate Receptors in the Processes Underlying Neurodegeneration
Published 2015-01-01“…Under clinical conditions, hyperactivity of the glutamate system is associated with ischemia, epilepsy, and neurodegenerative diseases such as Alzheimer’s, Huntington’s, and many others. …”
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442
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443
NREM and REM sleep parasomnias: clinical cases and literature review
Published 2021-06-01“…Detailed sleep history and clinical examination are of essential significance in differential diagnosis between sleep disorders, nocturnal epilepsy, and psychiatric disorders. Non-pharmacological interventions such as sleep hygiene and safe sleeping environment play an important role in management of parasomnias. …”
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444
Strategies to innovate emergency care of status epilepticus
Published 2025-01-01“…Many patients with medically refractory epilepsy are at risk for SE. Newly available nasally delivered benzodiazepines: midazolam and diazepam given for seizure clusters may prevent SE. …”
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445
A human single-neuron dataset for object recognition
Published 2025-01-01“…Here, we recorded single-neuron activity from the human amygdala and hippocampus when neurosurgical epilepsy patients performed a one-back task using naturalistic object stimuli. …”
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446
Factors Associated with Chronic Noncancer Pain in the Canadian Population
Published 2009-01-01“…A number of comorbid medical illnesses increased CNCP risk, including some (such as chronic obstructive pulmonary disease, epilepsy and thyroid disease) that have not hitherto been associated with pain. …”
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447
Widespread Striatal Delivery of GDNF from Encapsulated Cells Prevents the Anatomical and Functional Consequences of Excitotoxicity
Published 2019-01-01“…Because GDNF has been effective in animal models of Parkinson’s disease, stroke, epilepsy, and Huntington’s disease, among other debilitating neurodegenerative diseases, encapsulated cell-based delivery of GDNF might represent one innovative means of slowing the neural degeneration seen in a myriad of currently untreatable neurological diseases.…”
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448
The cellular distribution of P2X7, P2Y6, and P2Y12 during or after pilocarpine-induced status epilepticus and literature review
Published 2024-12-01“…Our literature review revealed that P2X7, P2Y6, and P2Y12 are expressed in different cells during epilepsy pathogenesis. Therefore, we studied the protein expression patterns of the purinergic receptors P2X7, P2Y6, and P2Y12 in the normal mice hippocampus, as well as during or after pilocarpine-induced status epilepticus (DPISE or APISE). …”
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449
Infection-Induced Elevated Plasma Perampanel in a Patient with Hemimegalencephaly
Published 2022-01-01“…The patient had refractory epilepsy associated with hemimegalencephaly. During adolescence, perampanel (maximum dose, 10 mg, oral), valproic acid, clobazam, and lacosamide were administered for seizure control. …”
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450
Treatment of convulsive status epilepticus in Brazil: a review
Published 2025-01-01“…Status epilepticus (SE) is the most severe presentation of epilepsy. Currently, SE is defined according to 2 sequential time frames: time 1, after which it is unlikely that the seizure will resolve spontaneously, therefore requiring the initiation of therapy; and time 2, when long-term consequences become more likely. …”
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451
Dravet Syndrome in Lebanon: First Report on Cases with SCN1A Mutations
Published 2019-01-01“…Dravet syndrome, also known as severe myoclonic epilepsy in infancy, is a rare disease characterized by the appearance of different types of seizures in a healthy baby, triggered by various factors and stressful events. …”
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452
Novel strategies targeting mitochondria-lysosome contact sites for the treatment of neurological diseases
Published 2025-01-01“…Emerging evidence suggests that abnormalities in mitochondria-lysosome contact sites (MLCSs) contribute to neurological diseases, including Parkinson’s disease, Charcot–Marie-Tooth (CMT) disease, lysosomal storage diseases, and epilepsy. This article reviews recent research advances regarding the tethering processes, regulation, and function of MLCSs and their role in neurological diseases.…”
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453
A Case of Anorexia Nervosa with Focal Cortical Dysplasia
Published 2024-01-01“…Focal cortical dysplasia (FCD) is characterized by dysplasia of the cerebral cortex and is a common cause of pharmacoresistant epilepsy. However, FCD associated with AN has never been reported. …”
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454
Pharmacovigilance of carbamazepine at the Marta Abreu Polyclinic. Santa Clara, 2022
Published 2023-02-01“…<br /><strong>Results:</strong> the age group from 51 to 60 predominated with 43 patients (20.5%), within this group the female sex (11.0% of the total); the predominant diagnosis was generalized epilepsy with a total of 93 patients. The female sex predominated with a total of 59 patients and in them the largest number of expired files was found, with a total of 16. …”
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455
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456
Can Chaotic Analysis of Electroencephalogram Aid the Diagnosis of Encephalopathy?
Published 2018-01-01“…Chaotic features of electroencephalogram have been analyzed in various disease states like epilepsy, Alzheimer’s disease, sleep disorders, and depression. …”
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457
An induced pluripotent stem cell line, NIMHi014-A, generated from PBMCs of an epileptic patient harbouring a variant of the SCN1A gene
Published 2025-04-01“…This cell line will be used to study mechanism of epilepsy and develop patient specific therapies.…”
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458
Persistent Visual Aura following Catheter Ablation in a Patient with WPW Syndrome
Published 2007-01-01“…Her visual symptoms were very similar to those of visual aura of migraine, rather than those of photosensitive epilepsy. Magnetic resonance imaging (MRI) and single photon emission computed tomography (SPECT), electroenchepalogram (EEG), and visual-evoked potentials (VEP) in the patient were normal. …”
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459
Modulation of Astrocytes on Mode Selection of Neuron Firing Driven by Electromagnetic Induction
Published 2020-01-01“…Indeed, the combination of the two factors and appropriate choice of parameters show the great potential to control disorder of neuron firing like epilepsy.…”
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460
Clinical and molecular outcomes from the 5-Year natural history study of SSADH Deficiency, a model metabolic neurodevelopmental disorder
Published 2024-04-01“…Language developmental delays were more prominent than motor. Autism, epilepsy, movement disorders, sleep disturbances, and various psychiatric behaviors constituted the core of the disorder’s clinical phenotype. …”
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