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You searched for: Author/Creator Pedrazzini, Matteo

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1. Estimating the Posttest Probability of Long QT Syndrome Diagnosis for Rare KCNH2 Variants. (26th July 2021)

3. MTMR4 SNVs modulate ion channel degradation and clinical severity in congenital long QT syndrome: insights in the mechanism of action of protective modifier genes. Issue 3 (16th March 2020)

4. 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)

5. 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)

6. Oxidized LDL‐dependent pathway as new pathogenic trigger in arrhythmogenic cardiomyopathy. Issue 9 (2nd August 2021)

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

8. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome. Issue 4 (28th July 2020)