Pages that link to "Q33156860"
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The following pages link to Identification of a possible pathogenic link between congenital long QT syndrome and epilepsy (Q33156860):
Displaying 50 items.
- Altered cardiac electrophysiology and SUDEP in a model of Dravet syndrome (Q21089741) (← links)
- Drugs and Brugada syndrome patients: review of the literature, recommendations, and an up-to-date website (www.brugadadrugs.org) (Q24654954) (← links)
- Potassium Channels and Human Epileptic Phenotypes: An Updated Overview (Q26750434) (← links)
- hERG channel function: beyond long QT (Q27008078) (← links)
- Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype (Q27303611) (← links)
- Sudden cardiac arrest in people with epilepsy in the community: Circumstances and risk factors. (Q27348996) (← links)
- Mechanisms of sudden unexplained death in epilepsy (Q28081176) (← links)
- 2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: The Task Force for the Management of Patients with Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death of [...] (Q28087002) (← links)
- Sudden unexpected death in epilepsy: risk factors and potential pathomechanisms (Q28254409) (← links)
- Sudden unexpected death in epilepsy: from the lab to the clinic setting (Q28285414) (← links)
- Kv1.1 potassium channel deficiency reveals brain-driven cardiac dysfunction as a candidate mechanism for sudden unexplained death in epilepsy. (Q30494617) (← links)
- Assessment of the QT interval in the electroencephalography (EEG) of children with syncope, epilepsy, and attention-deficit hyperactivity disorder (ADHD). (Q33157743) (← links)
- Comparison of corrected QT interval as measured on electroencephalography versus 12-lead electrocardiography in children with a history of syncope (Q33160105) (← links)
- KCNH2 gene mutation: a potential link between epilepsy and long QT-2 syndrome. (Q33161213) (← links)
- Concealed long QT syndrome and intractable partial epilepsy: a case report (Q33161883) (← links)
- Convulsive Syncope Induced by Ventricular Arrhythmia Masquerading as Epileptic Seizures: Case Report and Literature Review (Q33167451) (← links)
- Beyond the Electrocardiogram: Mutations in Cardiac Ion Channel Genes Underlie Nonarrhythmic Phenotypes (Q33565907) (← links)
- Drug-induced QT interval shortening: potential harbinger of proarrhythmia and regulatory perspectives (Q33661027) (← links)
- HERG1 channelopathies (Q33915930) (← links)
- Systems pharmacology of arrhythmias (Q34111154) (← links)
- High-resolution molecular genomic autopsy reveals complex sudden unexpected death in epilepsy risk profile (Q34331927) (← links)
- Epilepsy is a risk factor for sudden cardiac arrest in the general population (Q34391007) (← links)
- Another cause of sudden infant death syndrome: report of a clinical case of congenital long QT syndrome (Q35049104) (← links)
- Explaining the unexplained; expecting the unexpected: where are we with sudden unexpected death in epilepsy? (Q35052178) (← links)
- Increased prevalence of ECG markers for sudden cardiac arrest in refractory epilepsy (Q35134455) (← links)
- Importance of cardiological evaluation for first seizures. (Q35335917) (← links)
- Cardiac arrhythmias and ictal events within an epilepsy monitoring unit (Q36443569) (← links)
- Schizophrenia-Associated hERG channel Kv11.1-3.1 Exhibits a Unique Trafficking Deficit that is Rescued Through Proteasome Inhibition for High Throughput Screening (Q36583015) (← links)
- A common missense variant in the neuregulin 1 gene is associated with both schizophrenia and sudden cardiac death (Q36954999) (← links)
- Cardiac arrhythmia in a mouse model of sodium channel SCN8A epileptic encephalopathy (Q37417878) (← links)
- Sudden adult death (Q37556149) (← links)
- Tbx20 controls the expression of the KCNH2 gene and of hERG channels (Q37599006) (← links)
- Genomic biomarkers of SUDEP in brain and heart (Q37707209) (← links)
- Genetic basis of malignant channelopathies and ventricular fibrillation in the structurally normal heart (Q37749844) (← links)
- Post-mortem review and genetic analysis of sudden unexpected death in epilepsy (SUDEP) cases. (Q37793374) (← links)
- Part 12: Education, implementation, and teams: 2010 International Consensus on Cardiopulmonary Resuscitation and Emergency Cardiovascular Care Science with Treatment Recommendations (Q37801119) (← links)
- The serotonin axis: Shared mechanisms in seizures, depression, and SUDEP. (Q37826768) (← links)
- When your child with epilepsy dies suddenly: febrile seizures are part of the process? (Q37882438) (← links)
- Autonomic epileptic seizures, autonomic effects of seizures, and SUDEP. (Q38055646) (← links)
- Activity-dependent callosal axon projections in neonatal mouse cerebral cortex (Q38065150) (← links)
- QTc prolongation by antiepileptic drugs and the risk of torsade de pointes in patients with epilepsy (Q38065495) (← links)
- Sudden unexpected death in Dravet syndrome: respiratory and other physiological dysfunctions (Q38121340) (← links)
- Research advances in basic mechanisms of seizures and antiepileptic drug action (Q38154412) (← links)
- Increasing awareness of sudden unexpected death in epilepsy (Q38162943) (← links)
- Mechanisms of sudden unexpected death in epilepsy: the pathway to prevention (Q38206101) (← links)
- Cardiac channel molecular autopsy for sudden unexpected death in epilepsy (Q38417008) (← links)
- Diagnostic Approach to Genetic Causes of Early-Onset Epileptic Encephalopathy (Q38566303) (← links)
- KCNT1 mutations in seizure disorders: the phenotypic spectrum and functional effects. (Q38689167) (← links)
- Sudden unexpected death in epilepsy: basic mechanisms and clinical implications for prevention. (Q38775736) (← links)
- Large-scale mutational analysis of Kv11.1 reveals molecular insights into type 2 long QT syndrome (Q38938416) (← links)