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11. Mutation location and I  Ks regulation in the arrhythmic risk of long QT syndrome type 1: the importance of the KCNQ1 S6 region. (10th September 2021)

12. Mutation location and IKs regulation in the arrhythmic risk of long QT syndrome type 1: the importance of the KCNQ1 S6 region. (10th September 2021)

13. Response by Crotti et al to Letter Regarding Article, "Genetic Modifiers for the Long-QT Syndrome: How Important Is the Role of Variants in the 3′ Untranslated Region of KCNQ1?". (December 2016)

14. Response to Letters Regarding Article, "Clinical Management of Catecholaminergic Polymorphic Ventricular Tachycardia: The Role of Left Cardiac Sympathetic Denervation". Issue 4 (26th January 2016)

15. SCN5A mutations in 442 neonates and children: genotype–phenotype correlation and identification of higher-risk subgroups. (27th July 2018)

16. The genetics underlying acquired long QT syndrome: impact for genetic screening. (28th December 2015)

17. The genetics underlying idiopathic ventricular fibrillation: A special role for catecholaminergic polymorphic ventricular tachycardia?. (1st January 2018)