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

15. Concealed Inherited Cardiomyopathies Detected in Cardio-Oncology Screening

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

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

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

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

24. Clinical Evaluation of Patients with Genetically Confirmed Familial Hypercholesterolemia

26. Natural History of MYH7-Related Dilated Cardiomyopathy

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

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

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

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

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

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

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

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

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

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

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

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

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

43. Characterization of Left Ventricular Non-Compaction Cardiomyopathy

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

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

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

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

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

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