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You searched for: Author/Creator Gerull, Brenda

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1. A homozygous DSC2 deletion associated with arrhythmogenic cardiomyopathy is caused by uniparental isodisomy. (April 2020)

2. Antisense‐mediated exon skipping: a therapeutic strategy for titin‐based dilated cardiomyopathy. Issue 5 (10th March 2015)

3. Biallelic mutation in MYH7 and MYBPC3 leads to severe cardiomyopathy with left ventricular noncompaction phenotype. Issue 8 (24th April 2019)

4. Cardiac Abnormalities in First-Degree Relatives of Unexplained Cardiac Arrest Victims: A Report From the Cardiac Arrest Survivors With Preserved Ejection Fraction Registry. (September 2016)

5. Functional characterization of the novel DES mutation p.L136P associated with dilated cardiomyopathy reveals a dominant filament assembly defect. (February 2016)

7. Genetic Testing in the Evaluation of Unexplained Cardiac Arrest: From the CASPER (Cardiac Arrest Survivors With Preserved Ejection Fraction Registry). (June 2017)

9. Loss-of-Function KCNE2 Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation?. (August 2017)

10. Mechanistic Insights of the LEMD2 p.L13R Mutation and Its Role in Cardiomyopathy. Issue 2 (4th January 2023)