Search

Search Constraints

You searched for: Author/Creator Klaassen, Sabine

Search Results

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

2. Diffuse myocardial fibrosis by T1 mapping is associated with heart failure in pediatric primary dilated cardiomyopathy. (15th June 2021)

3. Ebstein anomaly associated with left ventricular noncompaction: An autosomal dominant condition that can be caused by mutations in MYH7. Issue 3 (21st June 2013)

4. External validation of the HCM Risk-Kids model for predicting sudden cardiac death in childhood hypertrophic cardiomyopathy. (31st October 2021)

5. Familial Recurrent Myocarditis Triggered by Exercise in Patients With a Truncating Variant of the Desmoplakin Gene. Issue 10 (18th May 2020)

7. Pathogenic Variants Associated With Dilated Cardiomyopathy Predict Outcome in Pediatric Myocarditis. (2nd July 2021)

8. Relationship Between Maximal Left Ventricular Wall Thickness and Sudden Cardiac Death in Childhood Onset Hypertrophic Cardiomyopathy. (2nd May 2022)

9. RIKADA Study Reveals Risk Factors in Pediatric Primary Cardiomyopathy. Issue 15 (6th August 2019)