Results 191 to 200 of about 202,862 (302)
Combined unipolar and bipolar voltage mapping for atrial substrate assessment: associations with arrhythmia recurrence after redo ablation. [PDF]
Mohsen Y +11 more
europepmc +1 more source
Abstract Epilepsy surgery offers a unique opportunity to connect clinical care with fundamental research on the human brain. Tissue resected as part of indicated surgical treatment can be studied using electrophysiology, imaging, transcriptomics, proteomics, connectomics, and computational modeling without altering the clinical procedure or exposing ...
Karl Roessler
wiley +1 more source
Scn1a‐mediated developmental regulation of prefrontal cortex plasticity and cognition
Abstract Objective The voltage‐gated sodium channel Nav1.1, encoded by Scn1a, is essential for γ‐aminobutyric acid (GABA)ergic function, and its alteration is associated with neurological disorders such as Dravet syndrome and Alzheimer's disease. We previously demonstrated that local Nav1.1 dysfunction in the medial prefrontal cortex (mPFC) during ...
Maurizio S. Riga +5 more
wiley +1 more source
Zwitterionic Polymer Coating Enabled Chronic Dopamine Sensing and Electrophysiology Recording in Free-Moving Mice. [PDF]
Wu B +5 more
europepmc +1 more source
Kv3.1 activation suppresses provoked and spontaneous seizures in a mouse Dravet syndrome model
Abstract Objective γ‐Aminobutyric acidergic (GABAergic) parvalbumin‐positive (PV+) interneurons are critical for maintaining cortical inhibitory tone, with their dysfunction predictably leading to epilepsy. Rapid PV+ interneuron firing is essential for their normal function and is maintained in part by potassium voltage‐gated channels.
Sheryl Anne D. Vermudez +11 more
wiley +1 more source
Exercise-Provoked Wide-Complex Tachycardia and Extreme Duke Score: Orthodromic Reciprocating Tachycardia Unmasked by Electrophysiology Study. [PDF]
Ray N, Petty A, Money D, Bracewell N.
europepmc +1 more source
Abstract Objective Dravet syndrome (DS) is a developmental and epileptic encephalopathy primarily caused by haploinsufficiency of the SCN1A gene, which encodes the alpha subunit of NaV1.1 voltage‐gated sodium channel. The disease manifests with febrile and spontaneous seizures, developmental delay, cognitive impairment, and increased risk of sudden ...
Martina Mainardi +4 more
wiley +1 more source
Alternating bundle branch block and infra-Hisian Mobitz II block: an educational case of rapidly progressive His-Purkinje disease. [PDF]
Hernandez S +4 more
europepmc +1 more source
Abstract Objective Mild malformation of cortical development with oligodendroglial hyperplasia and epilepsy (MOGHE) is a recently recognized cause of drug‐resistant focal epilepsy. It is often magnetic resonance imaging‐negative or radiologically resembles focal cortical dysplasias, which makes recognition difficult and limits presurgical counseling ...
Vadym Gnatkovsky +25 more
wiley +1 more source

