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You searched for: Author/Creator Iglesias, Anna

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1. A Missense Mutation in the Sodium Channel β2 Subunit Reveals SCN2B as a New Candidate Gene for Brugada Syndrome. Issue 7 (29th April 2013)

2. A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia. (January 2017)

3. Arrhythmogenic right ventricular cardiomyopathy: severe structural alterations are associated with inflammation. Issue 12 (3rd September 2012)

5. Corrigendum to "Further evidence of the association between LQT syndrome and epilepsy in a family with KCNQ1 pathogenic variant" [Seizure 25 (2015) 65–67]. (August 2015)

6. Front Cover: Integration of "Omics" Strategies for Biomarkers Discovery and for the Elucidation of Molecular Mechanisms Underlying Brugada Syndrome. Issue 6 (16th November 2018)

7. Further evidence of the association between LQT syndrome and epilepsy in a family with KCNQ1 pathogenic variant. (February 2015)

8. Further evidence of the association between LQT syndrome and epilepsy in a family with KCNQ1 pathogenic variant. (February 2015)

9. Genetic analysis in post-mortem samples with micro-ischemic alterations. (February 2017)