18 results on '"Van Tintelen JP"'
Search Results
2. P573Added diagnostic value of multiplex ligation-dependent probe amplification of plakophilin-2 in arrhythmogenic cardiomyopathy
3. Familial evaluation in catecholaminergic polymorphic ventricular tachycardia: disease penetrance and expression in cardiac ryanodine receptor mutation-carrying relatives.
4. Critical appraisal of the revised Ghent criteria for diagnosis of Marfan syndrome.
5. Desmin-related myopathy.
6. Arrhythmogenic right ventricular dysplasia/cardiomyopathy: pathogenic desmosome mutations in index-patients predict outcome of family screening: dutch arrhythmogenic right ventricular dysplasia/cardiomyopathy genotype-phenotype follow-up study.
7. Peripartum cardiomyopathy as a part of familial dilated cardiomyopathy.
8. Severe myocardial fibrosis caused by a deletion of the 5' end of the lamin A/C gene.
9. Molecular genetics of arrhythmogenic right ventricular cardiomyopathy: emerging horizon?
10. Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy.
11. Counsel the genotype, treat the phenotype.
12. P573 Added diagnostic value of multiplex ligation-dependent probe amplification of plakophilin-2 in arrhythmogenic cardiomyopathy.
13. P764 Phospholamban p.Arg14del-mutation related cardiomyopathy is a biventricular arrhythmogenic cardiomyopathy and protein-aggregate associated disease.
14. Risk factors for malignant ventricular arrhythmias in lamin a/c mutation carriers a European cohort study.
15. Mortality risk of untreated Myosin-binding protein C-related hypertrophic cardiomyopathy insight into the natural history.
16. Distinguishing arrhythmogenic right ventricular cardiomyopathy/dysplasia-associated mutations from background genetic noise.
17. The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: a comprehensive open reading frame mutational analysis.
18. Developmental aspects of long QT syndrome type 3 Brugada syndrome on the basis of a single SCN5A mutation in childhood.
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