Pages that link to "Q33158197"
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The following pages link to SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndrome (Q33158197):
Displaying 50 items.
- Next-Generation Sequencing in Post-mortem Genetic Testing of Young Sudden Cardiac Death Cases (Q26745883) (← links)
- The Brugada Syndrome: A Rare Arrhythmia Disorder with Complex Inheritance (Q26747227) (← links)
- Physiological and Pathophysiological Insights of Nav1.4 and Nav1.5 Comparison (Q26772794) (← links)
- Genetics of inherited primary arrhythmia disorders (Q26783570) (← links)
- Cellular hyper-excitability caused by mutations that alter the activation process of voltage-gated sodium channels (Q27008161) (← links)
- Electrophysiological Mechanisms of Brugada Syndrome: Insights from Pre-clinical and Clinical Studies (Q28073629) (← links)
- Recent advances in genetic testing and counseling for inherited arrhythmias (Q28074154) (← links)
- Genetics of Brugada syndrome (Q28074918) (← links)
- Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death (Q28294931) (← links)
- Genetics of sudden cardiac death syndromes (Q28307856) (← links)
- Molecular genetics and functional anomalies in a series of 248 Brugada cases with 11 mutations in the TRPM4 channel (Q28485378) (← links)
- Clinical and electrophysiological profile of Brugada syndrome in the Tunisian population. (Q33159316) (← links)
- Genetic variants in SCN5A promoter are associated with arrhythmia phenotype severity in patients with heterozygous loss-of-function mutation (Q33161026) (← links)
- The Diagnosis, Risk Stratification, and Treatment of Brugada Syndrome (Q33165991) (← links)
- Risk Stratification and Therapeutic Approach in Brugada Syndrome (Q33166768) (← links)
- IRX3 variant as a modifier of Brugada syndrome with frequent ventricular fibrillation (Q33644313) (← links)
- An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing (Q33655317) (← links)
- A mutation in the CACNA1C gene leads to early repolarization syndrome with incomplete penetrance: A Chinese family study (Q33664288) (← links)
- Impact of genetics on the clinical management of channelopathies (Q34036797) (← links)
- SCN5A mutations in Brugada syndrome are associated with increased cardiac dimensions and reduced contractility (Q34372532) (← links)
- J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge (Q34534329) (← links)
- A novel missense mutation, I890T, in the pore region of cardiac sodium channel causes Brugada syndrome (Q34544772) (← links)
- SCN5A variation is associated with electrocardiographic traits in the Jackson Heart Study. (Q34827081) (← links)
- Complex genetic background in a large family with Brugada syndrome (Q35294252) (← links)
- Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome (Q35730438) (← links)
- Diagnostic dilemmas: overlapping features of brugada syndrome and arrhythmogenic right ventricular cardiomyopathy (Q35982138) (← links)
- Fever-Induced Brugada Syndrome (Q36103243) (← links)
- Ionic and cellular mechanisms underlying the development of acquired Brugada syndrome in patients treated with antidepressants. (Q36310359) (← links)
- SCN4A variants and Brugada syndrome: phenotypic and genotypic overlap between cardiac and skeletal muscle sodium channelopathies (Q36585034) (← links)
- Brugada syndrome in a family with a high mortality rate: a case report. (Q36741364) (← links)
- Cardiac sodium channel mutations: why so many phenotypes? (Q36932045) (← links)
- Dysfunction of the Voltage-Gated K Channel β2 Subunit in a Familial Case of Brugada Syndrome (Q37076110) (← links)
- Genetics can contribute to the prognosis of Brugada syndrome: a pilot model for risk stratification (Q37102131) (← links)
- Genetic Test for the Channelopaties: Useful or Less Than Useful for Patients? (Part II) (Q37313376) (← links)
- Computational tools to investigate genetic cardiac channelopathies. (Q37414102) (← links)
- Recent genetic discoveries implicating ion channels in human cardiovascular diseases (Q37699206) (← links)
- Genetic basis of malignant channelopathies and ventricular fibrillation in the structurally normal heart (Q37749844) (← links)
- Phenotypical Manifestations of Mutations in the Genes Encoding Subunits of the Cardiac Sodium Channel (Q37860068) (← links)
- Brugada syndrome: an update (Q38086845) (← links)
- Cardiac sodium channelopathy associated with SCN5A mutations: electrophysiological, molecular and genetic aspects (Q38118751) (← links)
- Genetic testing for inherited cardiac disease (Q38125385) (← links)
- Genetic biomarkers in Brugada syndrome. (Q38125767) (← links)
- Drug-induced Brugada syndrome by noncardiac agents (Q38132928) (← links)
- Genetics of sudden cardiac death caused by ventricular arrhythmias (Q38169914) (← links)
- Brugada syndrome: a heterogeneous disease with a common ECG phenotype? (Q38176956) (← links)
- New electrocardiographic features in Brugada syndrome (Q38211723) (← links)
- Reduced Penetrance and Variable Expression of SCN5A Mutations and the Importance of Co-inherited Genetic Variants: Case Report and Review of the Literature. (Q38221847) (← links)
- Genotype phenotype associations across the voltage-gated sodium channel family (Q38243946) (← links)
- The role of genetic testing in unexplained sudden death (Q38542918) (← links)
- The cardiac sodium channel gene SCN5A and its gene product NaV1.5: Role in physiology and pathophysiology. (Q38585131) (← links)