237 results on '"Lopes, Luis R"'
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2. Phenotype and Clinical Outcomes in Desmin-Related Arrhythmogenic Cardiomyopathy
3. Improved Diagnostic Criteria for Apical Hypertrophic Cardiomyopathy
4. Predicted Deleterious Variants in Cardiomyopathy Genes Prognosticate Mortality and Composite Outcomes in the UK Biobank
5. Electrophysiological Characterization of Subclinical and Overt Hypertrophic Cardiomyopathy by Magnetic Resonance Imaging-Guided Electrocardiography
6. Embarazo en mujeres portadoras de variantes genéticas de miocardiopatía dilatada
7. Pregnancy in women with dilated cardiomyopathy genetic variants
8. Alpha kinase 3 signaling at the M-band maintains sarcomere integrity and proteostasis in striated muscle
9. Structure determination and analysis of titin A-band fibronectin type III domains provides insights for disease-linked variants and protein oligomerisation
10. Natural History of MYH7-Related Dilated Cardiomyopathy
11. Microstructural and Microvascular Phenotype of Sarcomere Mutation Carriers and Overt Hypertrophic Cardiomyopathy
12. Detection of subclinical hypertrophic cardiomyopathy
13. Prevalence, Cardiac Phenotype, and Outcomes of Transthyretin Variants in the UK Biobank Population.
14. An overview of heart rhythm disorders and management in myotonic dystrophy type 1
15. Correlación genotipo-fenotipo en miocardiopatía hipertrófica: un estudio multicéntrico en Portugal y España sobre la variante p.Arg21Leu de TPM1
16. Precision measurement of cardiac structure and function in cardiovascular magnetic resonance using machine learning
17. The Novel Desmin Variant p.Leu115Ile Is Associated With a Unique Form of Biventricular Arrhythmogenic Cardiomyopathy
18. Diagnosis and risk stratification in hypertrophic cardiomyopathy using machine learning wall thickness measurement: a comparison with human test-retest performance
19. Abstract 13516: Natural History, Penotypes and Clinical Outcomes in Desmin Related Arrhythmogenic Cardiomyopathy
20. Frequency, Penetrance, and Variable Expressivity of Dilated Cardiomyopathy–Associated Putative Pathogenic Gene Variants in UK Biobank Participants
21. Genetics of hypertrophic cardiomyopathy: established and emerging implications for clinical practice.
22. Distal Ventricular Pacing for Drug-Refractory Mid- Cavity Obstructive Hypertrophic Cardiomyopathy: A Randomized, Placebo-Controlled Trial of Personalized Pacing.
23. The p.(Cys150Tyr) variant in CSRP3 is associated with late-onset hypertrophic cardiomyopathy in heterozygous individuals
24. Patient-derived induced pluripotent stem cells to study non-canonical splicing variants associated with Hypertrophic Cardiomyopathy
25. Improved Diagnostic Criteria for Apical Hypertrophic Cardiomyopathy
26. Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy
27. Predicted Deleterious Variants in Cardiomyopathy Genes Prognosticate Mortality and Composite Outcomes in UK Biobank
28. Unlocking Predictive Power: A Machine Learning Tool Derived from In-Depth Analysis to Forecast the Impact of Missense Variants in Human Filamin C
29. Apical Ischemia Is a Universal Feature of Apical Hypertrophic Cardiomyopathy
30. Genome-Wide Analysis of Left Ventricular Maximum Wall Thickness in the UK Biobank Cohort Reveals a Shared Genetic Background With Hypertrophic Cardiomyopathy
31. Integrin α7 Mutations Are Associated With Adult‐Onset Cardiac Dysfunction in Humans and Mice
32. Natural History of MYH7-Related Dilated Cardiomyopathy
33. Alpha kinase 3 signaling at the M-band maintains sarcomere integrity and proteostasis in striated muscle
34. Early Childhood-Onset Hypertrophic Cardiomyopathy in a Family With an In-Frame MYH7 Deletion
35. Relationship between aetiology and left ventricular systolic dysfunction in hypertrophic cardiomyopathy
36. Association between common cardiovascular risk factors and clinical phenotype in patients with hypertrophic cardiomyopathy from the European Society of Cardiology (ESC) EurObservational Research Programme (EORP) Cardiomyopathy/Myocarditis registry
37. Frequency, Penetrance, and Variable Expressivity of Dilated Cardiomyopathy-Associated Putative Pathogenic Gene Variants in UK Biobank Participants
38. The Frequency, Penetrance and Variable Expressivity of Dilated Cardiomyopathy-Associated Putative Pathogenic Gene Variants in UK Biobank Participants
39. 20 Apical ischaemia is ubiquitous in apical hypertrophic cardiomyopathy and occurs before overt hypertrophy
40. Phenotyping hypertrophic cardiomyopathy using cardiac diffusion magnetic resonance imaging: the relationship between microvascular dysfunction and microstructural changes
41. The UK10K project identifies rare variants in health and disease
42. Novel genotype-phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy
43. Prognostic relevance of exercise testing in hypertrophic cardiomyopathy. A systematic review
44. Cardiac myosin binding protein-C variants in paediatric-onset hypertrophic cardiomyopathy: natural history and clinical outcomes
45. Myocardial Perfusion Defects in Hypertrophic Cardiomyopathy Mutation Carriers
46. Alpha-protein kinase 3 (ALPK3) truncating variants are a cause of autosomal dominant hypertrophic cardiomyopathy
47. Prevalence of Hypertrophic Cardiomyopathy in the UK Biobank Population
48. Association between common cardiovascular risk factors and clinical phenotype in patients with hypertrophic cardiomyopathy from the European Society of Cardiology (ESC) EurObservational Research Programme (EORP) Cardiomyopathy/Myocarditis registry
49. Iterative Reanalysis of Hypertrophic Cardiomyopathy Exome Data Reveals Causative Pathogenic Mitochondrial DNA Variants
50. Cardiac myosin binding protein-C variants in paediatric-onset hypertrophic cardiomyopathy: natural history and clinical outcomes.
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