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4. Natural History of MYH7-Related Dilated Cardiomyopathy

5. “Inherited cardiovascular disease mindset” can identify concealed inherited conditions at cardio-oncology evaluation: An opportunistic screening.

10. Concealed Inherited Cardiomyopathies Detected in Cardio-Oncology Screening

11. Retrospective variant reclassification and resequencing in hypertrophic cardiomyopathy: A Reference Unit Centre Experience.

13. Concealed Inherited Cardiomyopathies Detected in Cardio-Oncology Screening.

15. Mitochondrial Heteroplasmy as a Marker for Premature Coronary Artery Disease: Analysis of the Poly-C Tract of the Control Region Sequence

16. Opportunistic Genetic Screening for Familial Hypercholesterolemia in Heart Transplant Patients

17. Clinical Evaluation of Patients with Genetically Confirmed Familial Hypercholesterolemia

18. Chromosome Y Haplogroup R Was Associated with the Risk of Premature Myocardial Infarction with ST-Elevation: Data from the CholeSTEMI Registry.

19. Natural History of MYH7-Related Dilated Cardiomyopathy

20. Different Phenotypes in Monozygotic Twins, Carriers of the Same Pathogenic Variant for Hypertrophic Cardiomyopathy

22. Association of the Genetic Variation in the Long Non-Coding RNA FENDRR with the Risk of Developing Hypertrophic Cardiomyopathy

23. Genetic Screening of a Large Panel of Genes Associated with Cardiac Disease in a Spanish Heart Transplanted Cohort

24. KCNH2 p.Gly262AlafsTer98: A New Threatening Variant Associated with Long QT Syndrome in a Spanish Cohort

25. Permanent Pacemaker Reduction Using Cusp-Overlapping Projection in TAVR

26. STEMI, primary percutaneous coronary intervention and recovering of life expectancy: insights from the SurviSTEMI study

28. Founder mutation in myosin-binding protein C with an early onset and a high penetrance in males

29. Frailty Assessment in a Cohort of Elderly Patients with Severe Symptomatic Aortic Stenosis: Insights from the FRailty Evaluation in Severe Aortic Stenosis (FRESAS) Registry

30. Evaluation of cardiovascular events in patients with hepatocellular carcinoma treated with sorafenib in the clinical practice. The CARDIO‐SOR study

31. Premature STEMI in Men and Women: Current Clinical Features and Improvements in Management and Prognosis

32. Compound heterozygosity for PTPN11 variants in a subject with Noonan syndrome provides insights into the mechanism of SHP2 ‐related disorders

33. IL17RA in early-onset coronary artery disease: Total leukocyte transcript analysis and promoter polymorphism (rs4819554) association

34. Angiotensin-converting enzymes (ACE, ACE2) gene variants and COVID-19 outcome

35. Clinical Implications and Gender Differences of KCNQ1 p.Gly168Arg Pathogenic Variant in Long QT Syndrome

36. Familial Hypercholesterolemia in Premature Acute Coronary Syndrome. Insights from CholeSTEMI Registry

37. Characterization of Left Ventricular Non-Compaction Cardiomyopathy

39. Long term follow up of percutaneous treatment for degenerated Mitroflow prosthesis with self-expanding transcatheter aortic valve implantation

40. Percutaneous treatment with Mitraclip for functional mitral regurgitation: medium-term follow up according to left ventricular function

41. Coexistence of transmural and lateral wavefront progression of myocardial infarction in the human heart

42. Initial experience of a MitraClip valve repair program in Spain

43. Outcomes with percutaneous mitral repair vs. optimal medical treatment for functional mitral regurgitation: systematic review

46. Angiotensin-converting enzyme (ACE1, ACE2) gene variants are associated with COVID19 severity depending on the hypertension status

47. Transcatheter Mitral Repair for Functional Mitral Regurgitation According to Left Ventricular Function: A Real-Life Propensity-Score Matched Study

48. Observed and Expected Survival in Men and Women after Suffering a STEMI

49. Coexistence of transmural and lateral wavefront progression of myocardial infarction in the human heart.

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