25 results for “epilepsy”. Showing 25 of 39,449.
Wnt/β-catenin signalling pathway mediated aberrant hippocampal neurogenesis in kainic acid-induced epilepsy.
epilepsy. Temporal lobe epilepsy is a chronic disorder of nerve
AMPK role in epilepsy: a promising therapeutic target?
epilepsy. Due to the complicated nature of refractory epilepsy, other
Genetic heterogeneity in epilepsy and comorbidities: insights from Pakistani families.
Epilepsy, a challenging neurological condition, is often present with comorbidities
Recent advances and current status of gene therapy for epilepsy.
Epilepsy is a common neurological disorder with complex pathogenic mechanisms
mTOR and neuroinflammation in epilepsy: implications for disease progression and treatment.
Epilepsy remains a major health concern as anti-seizure medications
Phenylbutyrate for monogenetic epilepsy: Literature review.
epilepsy. As many as 40 % of epilepsies are caused
Opposing effects of the purinergic P2X7 receptor on seizures in neurons and microglia in male mice.
epilepsy and patients. To date, the cell type-specific downstream
Updated clinical recommendations for the management of tuberous sclerosis complex associated epilepsy.
epilepsy remain a major challenge for clinicians. In 2018 clinical
Gene expression of the HCN family in rats with pilocarpine-induced epilepsy and in human hippocampal and cortical tissue.
Epilepsy is a chronic pathophysiological syndrome defined by excessive and recurrent
Glycoprotein Non-metastatic Melanoma Protein B (GPNMB) Protects Against Neuroinflammation and Neuronal Loss in Pilocarpine-induced Epilepsy via the Regulation of Microglial Polarization.
epilepsy. A proven model of epilepsy was established by intraperitoneal
Microglia in epilepsy.
epilepsy. Further exploration of the cellular or molecular mechanism of epilepsy
Exploring the clinical connections between epilepsy and diabetes mellitus: Promising therapeutic strategies utilizing agmatine and metformin.
epilepsy and the psychological and socio-economic implications that are associated
Expression of astrocyte-related receptors in cortical dysplasia with intractable epilepsy.
Epilepsy is one of the major neurologic diseases, and astrocytes
A Single-Cell Transcriptomic Atlas Elucidates a Microglial Gene Signature Linking Ferroptosis to Mitochondrial Dysfunction in Epilepsy.
Epilepsy is a chronic neurological disorder caused by abnormal synchronous
Functional stabilization of weakened thalamic pacemaker channel regulation in rat absence epilepsy.
epilepsy, but its distinct roles in epileptogenesis and chronic epilepsy
The microRNA-211-5p/P2RX7/ERK/GPX4 axis regulates epilepsy-associated neuronal ferroptosis and oxidative stress.
epilepsy. However, the mechanism of ferroptosis in epilepsy remains unclear
A mouse model of DEPDC5-related epilepsy: Neuronal loss of Depdc5 causes dysplastic and ectopic neurons, increased mTOR signaling, and seizure susceptibility.
epilepsy-related gene implicated in focal epilepsy, brain malformations, and Sudden
mtDNA leakage promotes neuron-glia crosstalk to induce epilepsy by cGAS-STING-driven neuroinflammation and serine metabolic reprogramming.
Epilepsy is increasingly recognized as a disorder involving metabolic dysregulation
Contribution of Somatic Ras/Raf/Mitogen-Activated Protein Kinase Variants in the Hippocampus in Drug-Resistant Mesial Temporal Lobe Epilepsy.
epilepsy (MTLE) is the most common focal epilepsy subtype and is often
Chandelier cells and epilepsy
epilepsy. In this article, it is proposed that the chandelier
Scorpion polypeptide BmK IT2 alleviates epileptic seizures and neuronal pyroptosis by regulating sodium channel Nav1.6.
Epilepsy is the fourth most common neurological disorder, and nearly
Construction of epilepsy diagnosis model based on cell senescence-related genes and its potential mechanism.
Epilepsy is a chronic brain disease with a certain degree
Comprehensive classification of HCN1 variants linked to neurodevelopmental disorders with and without epilepsy.
epilepsies. Here, we used patch-clamp electrophysiology in combination with
Epilepsy plus blindness in microdeletion of GABRA1 and GABRG2 in mouse and human.
epilepsy, including syndromic epilepsy. This report for the first time
Identification of epilepsy-associated neuronal subtypes and gene expression underlying epileptogenesis.
Epilepsy is one of the most common neurological disorders, yet its pathophysiology