Pages that link to "Q21089741"
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The following pages link to Altered cardiac electrophysiology and SUDEP in a model of Dravet syndrome (Q21089741):
Displaying 50 items.
- Sudden unexpected death in epilepsy: Identifying risk and preventing mortality (Q26780360) (← links)
- Pathogenesis and new candidate treatments for infantile spasms and early life epileptic encephalopathies: A view from preclinical studies (Q27308052) (← links)
- Mortality in Dravet syndrome: A review (Q28070017) (← links)
- Mechanisms of sudden unexplained death in epilepsy (Q28081176) (← links)
- Sodium channel β subunits: emerging targets in channelopathies (Q28082122) (← links)
- Cardiac Nav 1.5 is modulated by ubiquitin protein ligase E3 component n-recognin UBR3 and 6. (Q36057480) (← links)
- Influence of vigilance state on physiological consequences of seizures and seizure-induced death in mice. (Q37041589) (← links)
- Sudden unexpected death in epilepsy genetics: Molecular diagnostics and prevention (Q37279519) (← links)
- Cardiac arrhythmia in a mouse model of sodium channel SCN8A epileptic encephalopathy (Q37417878) (← links)
- Ion channels under the sun. (Q37702927) (← links)
- Antiepileptic Drugs Impair Shortening of Isolated Cardiomyocytes. (Q37734297) (← links)
- Mechanisms of sudden unexpected death in epilepsy: the pathway to prevention (Q38206101) (← links)
- Dravet syndrome--from epileptic encephalopathy to channelopathy (Q38212437) (← links)
- Untangling the dravet syndrome seizure network: the changing face of a rare genetic epilepsy (Q38215754) (← links)
- The genetics of the epilepsies. (Q38501842) (← links)
- Neonatal and Infantile Epilepsy: Acquired and Genetic Models (Q38659279) (← links)
- Neuronal hyperexcitability in a mouse model of SCN8A epileptic encephalopathy (Q38757993) (← links)
- Furthering our understanding of SUDEP: the role of animal models (Q38794020) (← links)
- Voltage-Gated Na Channels: Not Just for Conduction (Q38851171) (← links)
- Dravet Syndrome: Diagnosis and Long-Term Course. (Q38855478) (← links)
- Helping Families Cope with the Severe Stress of Dravet Syndrome (Q38855483) (← links)
- Genetic biomarkers for the risk of seizures in long QT syndrome (Q40537132) (← links)
- Genetic Basis of Sudden Unexpected Death in Epilepsy. (Q41061393) (← links)
- Dmpk gene deletion or antisense knockdown does not compromise cardiac or skeletal muscle function in mice (Q41643458) (← links)
- Altered GABAA receptor expression in brainstem nuclei and SUDEP in Gabrg2( /Q390X) mice associated with epileptic encephalopathy (Q42263969) (← links)
- Scn2b Deletion in Mice Results in Ventricular and Atrial Arrhythmias. (Q45991966) (← links)
- Modulation of Abnormal Sodium Channel Currents in Heart and Brain: Hope for SUDEP Prevention and Seizure Reduction (Q47112003) (← links)
- Functional Neuroplasticity in the Nucleus Tractus Solitarius and Increased Risk of Sudden Death in Mice with Acquired Temporal Lobe Epilepsy (Q47153583) (← links)
- Severe peri-ictal respiratory dysfunction is common in Dravet syndrome. (Q47658294) (← links)
- Voltage-Gated Sodium Channel β Subunits and Their Related Diseases. (Q47720312) (← links)
- Scn1b deletion leads to increased tetrodotoxin-sensitive sodium current, altered intracellular calcium homeostasis and arrhythmias in murine hearts (Q47736002) (← links)
- High-Efficiency Gene Transfection of Cells through Carbon Nanotube Arrays (Q51382528) (← links)
- Myocardial remodeling and susceptibility to ventricular tachycardia in a model of chronic epilepsy. (Q55080592) (← links)
- Preclinical Animal Models for Dravet Syndrome: Seizure Phenotypes, Comorbidities and Drug Screening. (Q55471525) (← links)
- A companion to the preclinical common data elements for physiologic data in rodent epilepsy models. A report of the TASK3 Physiology Working Group of the ILAE/AES Joint Translational Task Force (Q58572354) (← links)
- Channelopathy as a SUDEP Biomarker in Dravet Syndrome Patient-Derived Cardiac Myocytes (Q58711098) (← links)
- deletion fails to rescue premature lethality in two models of sodium channel epilepsy (Q62396400) (← links)
- Time of Day and a Ketogenic Diet Influence Susceptibility to SUDEP in Mice (Q64102396) (← links)
- SCN1B and SCN2B gene variants analysis in dravet syndrome patients: Analysis of 22 cases (Q64227402) (← links)
- Golgi localized β1-adrenergic receptors stimulate Golgi PI4P hydrolysis by PLCε to regulate cardiac hypertrophy (Q83229721) (← links)
- Sudden unexpected death in children with epilepsy: focus on dietary supplementation with omega-3 polyunsaturated fatty acids (Q86844055) (← links)
- More children with epilepsy are dying suddenly (Q87378520) (← links)
- Summary of the 2016 Partners Against Mortality in Epilepsy (PAME) Conference (Q89489260) (← links)
- Sudden unexpected death in epilepsy (Q89729147) (← links)
- Scurrying to Understand Sudden Expected Death in Epilepsy: Insights From Animal Models (Q90127012) (← links)
- Cardiac arrhythmias in Dravet syndrome: an observational multicenter study (Q90616519) (← links)
- Sexually Divergent Mortality and Partial Phenotypic Rescue After Gene Therapy in a Mouse Model of Dravet Syndrome (Q91923585) (← links)
- Identification of potential candidate genes and pathways in atrioventricular nodal reentry tachycardia by whole-exome sequencing (Q96167146) (← links)
- Cardiovascular complications of epileptic seizures (Q96588344) (← links)
- Autonomic and Cardiac Repolarization Lability in Long QT Syndrome Patients (Q99562390) (← links)