Pages that link to "Q38125385"
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The following pages link to Genetic testing for inherited cardiac disease (Q38125385):
Displaying 50 items.
- Exome sequencing identifies a mutation in the ACTN2 gene in a family with idiopathic ventricular fibrillation, left ventricular noncompaction, and sudden death (Q21146705) (← links)
- Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype (Q27303611) (← links)
- Molecular autopsy in victims of inherited arrhythmias (Q28069286) (← links)
- Genetics of Brugada syndrome (Q28074918) (← links)
- Mechanisms of sudden unexplained death in epilepsy (Q28081176) (← links)
- Channelopathies - emerging trends in the management of inherited arrhythmias (Q28085317) (← links)
- TECRL, a new life-threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT (Q29465809) (← links)
- Exome sequencing identifies a novel mutation in the MYH6 gene in a family with early-onset sinus node dysfunction, ventricular arrhythmias, and cardiac arrest (Q33640155) (← links)
- The Genetic Challenges and Opportunities in Advanced Heart Failure (Q33653498) (← links)
- Rapid molecular genetic diagnosis of hypertrophic cardiomyopathy by semiconductor sequencing. (Q33812972) (← links)
- A novel variant in TBX20 (p.D176N) identified by whole-exome sequencing in combination with a congenital heart disease related gene filter is associated with familial atrial septal defect (Q34173995) (← links)
- Inherited arrhythmia syndromes leading to sudden cardiac death in the young: a global update and an Indian perspective (Q34541889) (← links)
- Next-generation sequencing for the diagnosis of cardiac arrhythmia syndromes (Q35539126) (← links)
- Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study. (Q35661823) (← links)
- Utility and limitations of exome sequencing as a genetic diagnostic tool for conditions associated with pediatric sudden cardiac arrest/sudden cardiac death. (Q35863638) (← links)
- A Common Variant in SCN5A and the Risk of Ventricular Fibrillation Caused by First ST-Segment Elevation Myocardial Infarction (Q36249059) (← links)
- Sudden Unexplained Death - Treating the Family (Q36458885) (← links)
- Sudden unexpected death in epilepsy genetics: Molecular diagnostics and prevention (Q37279519) (← links)
- Clinical and genetic features of Australian families with long QT syndrome: A registry-based study. (Q37455113) (← links)
- Genetics of sudden cardiac death caused by ventricular arrhythmias (Q38169914) (← links)
- Sudden cardiac death in the young: the molecular autopsy and a practical approach to surviving relatives. (Q38375887) (← links)
- Cardiovascular genetics: technological advancements and applicability for dilated cardiomyopathy (Q38511012) (← links)
- The role of genetic testing in unexplained sudden death (Q38542918) (← links)
- TRPM4 in cardiac electrical activity (Q38566534) (← links)
- Distinguishing pathogenic mutations from background genetic noise in cardiology: the use of large genome databases for genetic interpretation. (Q38739078) (← links)
- Genetic testing for inheritable cardiac channelopathies. (Q38831527) (← links)
- Genetics of cardiovascular diseases: lessons learned from a decade of genomics research in Iceland (Q39443092) (← links)
- Autosomal Recessive Cardiomyopathy Presenting as Acute Myocarditis (Q40266436) (← links)
- A systematic analysis of genetic dilated cardiomyopathy reveals numerous ubiquitously expressed and muscle-specific genes (Q41330928) (← links)
- Human pluripotent stem cell models of cardiac disease: from mechanisms to therapies (Q41664792) (← links)
- Repeated molecular genetic analysis in Brugada syndrome revealed a novel disease-associated large deletion in the SCN5A gene (Q41903329) (← links)
- From whole exome sequencing to patient-specific therapy: another example of how basic research pays off in patient care (Q43228080) (← links)
- Molecular Autopsy for Sudden Death in the Young: Is Data Aggregation the Key? (Q47102396) (← links)
- Ajmaline blocks INa and IKr without eliciting differences between Brugada syndrome patient and control human pluripotent stem cell-derived cardiac clusters. (Q47144807) (← links)
- Targeted next generation sequencing in a young population with suspected inherited malignant cardiac arrhythmias (Q48223076) (← links)
- Application of Single-Nucleotide Polymorphism-Related Risk Estimates in Identification of Increased Genetic Susceptibility to Cardiovascular Diseases: A Literature Review (Q49464137) (← links)
- Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome (Q55422968) (← links)
- Computational models in cardiology (Q58561255) (← links)
- High-throughput genetic characterization of a cohort of Brugada syndrome patients (Q58880781) (← links)
- Complex roads from genotype to phenotype in dilated cardiomyopathy: scientific update from the Working Group of Myocardial Function of the European Society of Cardiology (Q62476511) (← links)
- Primary care providers' lived experiences of genetics in practice. (Q64902300) (← links)
- Arrhythmias: Opening Pandora's Box -- incidental genetic findings (Q87401764) (← links)
- Genetic Testing in Inherited Heart Diseases: Practical Considerations for Clinicians (Q88784273) (← links)
- Loss-of-Function Variants in Cytoskeletal Genes Are Associated with Early-Onset Atrial Fibrillation (Q89511645) (← links)
- The yield of postmortem genetic testing in sudden death cases with structural findings at autopsy (Q90168496) (← links)
- Whole exome sequencing in a large pedigree with DCM identifies a novel mutation in RBM20 (Q90476267) (← links)
- Establishing a new human hypertrophic cardiomyopathy-specific model using human embryonic stem cells (Q91410532) (← links)
- A tailored approach towards informing relatives at risk of inherited cardiac conditions: study protocol for a randomised controlled trial (Q91752278) (← links)
- Is variant pathogenicity in the eye of the beholder? A case of unexplained sudden cardiac arrest highlights the potentially dangerous role of historical rare variant compendia in SCN5A rare variant adjudication (Q92492503) (← links)
- Utility of genetic testing in athletes (Q92568756) (← links)