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2. Alpha-protein kinase 3 (ALPK3) truncating variants are a cause of autosomal dominant hypertrophic cardiomyopathy. (15th July 2021)

3. Cardiac myosin binding protein-C variants in paediatric-onset hypertrophic cardiomyopathy: natural history and clinical outcomes. Issue 8 (16th August 2021)

5. Dilated cardiomyopathy and arrhythmogenic left ventricular cardiomyopathy: a comprehensive genotype-imaging phenotype study. (16th July 2019)

6. Genetic complexity in hypertrophic cardiomyopathy revealed by high-throughput sequencing. Issue 4 (8th February 2013)

7. Novel genotype–phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy. Issue 4 (28th October 2014)

8. Phenotyping hypertrophic cardiomyopathy using cardiac diffusion magnetic resonance imaging: the relationship between microvascular dysfunction and microstructural changes. (25th October 2021)

9. Relationship between aetiology and left ventricular systolic dysfunction in hypertrophic cardiomyopathy. Issue 4 (24th October 2016)