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Search Results to Luisa Mestroni

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One or more keywords matched the following properties of Mestroni, Luisa

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overview We are interested in the genetic basis, pathogenic mechanisms and phenotype correlations of cardiomyopathies, in particular arrhythmogenic forms (ACM, ARVC, LVNC). Our Familial Cardiomyopathy Registry biobank includes >2000 subjects. Our tools include clinical genetics, bioinformatics, outcome studies, induced pluripotent stem cell models, -omics, cell biomechanics and tissue engineering. I serve as a cardiology mentor.

One or more keywords matched the following items that are connected to Mestroni, Luisa

Item TypeName
Academic Article Molecular genetics of dilated cardiomyopathy.
Academic Article Advances in molecular genetics of dilated cardiomyopathy. The Heart Muscle Disease Study Group.
Academic Article Molecular genetics of dilated cardiomyopathies.
Academic Article Genetics and genetic testing of dilated cardiomyopathy: a new perspective.
Academic Article [Genetics of dilated cardiomyopathies].
Academic Article Molecular genetics of dilated cardiomyopathy.
Academic Article Familial hypertrophic cardiomyopathy: clinical features, molecular genetics and molecular genetic testing.
Academic Article Lamin A/C gene and the heart: how genetics may impact clinical care.
Concept Genetics
Academic Article Genetics and genomics for the prevention and treatment of cardiovascular disease: update: a scientific statement from the American Heart Association.
Academic Article Arrhythmogenic right ventricular cardiomyopathy: From genetics to diagnostic and therapeutic challenges.
Grant Molecular Epidemiology of Dilated Cardiomyopath
Grant Genetics, Mechanisms and Clinical Phenotypes of Arrhythmogenic Cardiomyopathy
Academic Article Genetics of Dilated Cardiomyopathy: Clinical Implications.
Academic Article Genetics of dilated cardiomyopathy.
Academic Article Genetics of Dilated Cardiomyopathy.
Academic Article Integrated role of cardiac magnetic resonance and genetics in predicting left ventricular reverse remodelling in dilated and non-dilated cardiomyopathy.

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  • Genetics

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