46 results on '"Gallego-Delgado, María"'
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2. Prevalence of Cardiac Amyloidosis Among Elderly Patients With Recent-Onset Atrial Fibrillation: The PREVAL-ATTR Study
3. Relevancia del estudio genético de la amiloidosis cardíaca por transtiretina en el anciano
4. Natural History of MYH7-Related Dilated Cardiomyopathy
5. Clinical Risk Score to Predict Pathogenic Genotypes in Patients With Dilated Cardiomyopathy
6. Caracterización de la amiloidosis cardiaca hereditaria por transtirretina en España
7. Association of Genetic Variants With Outcomes in Patients With Nonischemic Dilated Cardiomyopathy
8. Una variante rara en HCN4 produce un fenotipo de hipertrabeculación/no compactación ventricular, dilatación auricular izquierda y bradicardia sinusal
9. Predictores de riesgo en una cohorte española con cardiolaminopatías. Registro REDLAMINA
10. Start-up of a Cardiology Day Hospital: Activity, Quality Care and Cost-effectiveness Analysis of the First Year of Operation
11. Variable Penetrance and Expressivity of a Rare Pore Loss-of-Function Mutation (p.L889V) of Nav1.5 Channels in Three Spanish Families.
12. Importance of genetic study in elderly patients with transthyretin cardiac amyloidosis
13. First Magnetic Resonance Managed by a Cardiology Department in the Spanish Public Healthcare System. Experience and Difficulties of an Innovative Model
14. Late gadolinium enhancement distribution patterns in non-ischaemic dilated cardiomyopathy: genotype–phenotype correlation
15. Myocardial Extracellular Volume Is Not Associated With Malignant Ventricular Arrhythmias in High-risk Hypertrophic Cardiomyopathy
16. Late gadolinium enhancement distribution patterns in non-ischaemic dilated cardiomyopathy: genotype–phenotype correlation.
17. Kiosk 5R-TB-02 - Prognostic Value of Different Echocardiographic and Cardiac Magnetic Resonance Parameters in Patients with AL Amyloidosis
18. Extracellular Volume Detects Amyloidotic Cardiomyopathy and Correlates With Neurological Impairment in Transthyretin-familial Amyloidosis
19. Case Report: Renal relapse after heart transplantation, induction, and autologous stem cell transplantation in a patient with AL amyloidosis with exclusive cardiac involvement
20. Natural History of MYH7-Related Dilated Cardiomyopathy
21. Combination of late gadolinium enhancement and genotype improves prediction of prognosis in non‐ischaemic dilated cardiomyopathy
22. Characterization of hereditary transthyretin cardiac amyloidosis in Spain
23. A rare HCN4 variant with combined sinus bradycardia, left atrial dilatation, and hypertrabeculation/left ventricular noncompaction phenotype
24. Cardiac extracellular volume quantified with T1 mapping techniques reflects degree of cardiac and neurological involvement in Hereditary Transthyretin Amyloidosis
25. Risk Predictors in a Spanish Cohort With Cardiac Laminopathies. The REDLAMINA Registry
26. Risk predictors in a Spanish cohort with cardiac laminopathies. The REDLAMINA registry
27. Characterization of hereditary transthyretin cardiac amyloidosis in Spain.
28. Puesta en marcha de un hospital de día del área del corazón: análisis de actividad, calidad y coste-efectividad en el primer año de funcionamiento
29. Una variante rara en HCN4produce un fenotipo de hipertrabeculación/no compactación ventricular, dilatación auricular izquierda y bradicardia sinusal
30. Primera resonancia magnética gestionada por cardiología en la red sanitaria pública española: experiencia y dificultades de un modelo innovador
31. Fibrinolisis repetida como tratamiento de disfunción trombótica de prótesis valve-in-valve en posición mitral
32. Repeat Fibrinolysis to Treat Thrombotic Dysfunction of a Mitral Valve-in-valve Prosthesis
33. Familial Paralysis of the Atrium Due to a Mutation in SCN5A
34. Adverse clinical course and poor prognosis of hypertrophic cardiomyopathy due to mutations in FHL1
35. Mitochondrial Cardiomyopathies Associated With the m.3243A>G Mutation in the MT-TL1 Gene: Two Sides of the Same Coin
36. El volumen extracelular no se asocia a arritmias malignas en miocardiopatía hipertrófica de alto riesgo
37. Aplicación práctica de la genética en el manejo de las miocardiopatías
38. El volumen extracelular detecta la amiloidosis cardiaca y está correlacionado con el deterioro neurológico en la amiloidosis familiar relacionada con la transtiretina
39. Parálisis auricular familiar debida a una mutación en SCN5A
40. Miocardiopatías mitocondriales asociadas a la mutación m.3243A>G en el gen MT-TL1: dos caras de la misma moneda
41. Miocardiopatías mitocondriales asociadas a la mutación m.3243A>G en el gen MT-TL1:dos caras de la misma moneda
42. Caracterización de la amiloidosis cardiaca hereditaria por transtirretina en España
43. Fibrinolisis repetida como tratamiento de disfunción trombótica de prótesis valve-in-valveen posición mitral
44. Penetrance of Dilated Cardiomyopathy in Genotype-Positive Relatives.
45. Late gadolinium enhancement distribution patterns in non-ischaemic dilated cardiomyopathy: genotype-phenotype correlation.
46. Impact of SARS-Cov-2 infection in patients with hypertrophic cardiomyopathy: results of an international multicentre registry.
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