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You searched for: Author/Creator Coll, Monica

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

2. 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)

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

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

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

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

7. Genetic interpretation and clinical translation of minor genes related to Brugada syndrome. Issue 6 (29th March 2019)

8. Integration of "Omics" Strategies for Biomarkers Discovery and for the Elucidation of Molecular Mechanisms Underlying Brugada Syndrome. Issue 6 (20th July 2018)

9. Molecular autopsy in a cohort of infants died suddenly at rest. (November 2018)