Angela
López Sainz
Publicaciones (29) Publicaciones de Angela López Sainz
2023
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Hyperuricaemia Does Not Interfere with Aortopathy in a Murine Model of Marfan Syndrome
International Journal of Molecular Sciences, Vol. 24, Núm. 14
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Marfan syndrome in a paediatric cohort: The importance of family history
Cardiology in the Young, Vol. 35
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Mid-aortic Syndrome in a Pediatric Cohort
Pediatric Cardiology, Vol. 44, Núm. 1, pp. 168-178
2022
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Aortic flow dynamics and stiffness in Loeys-Dietz syndrome patients: a comparison with healthy volunteers and Marfan syndrome patients
European heart journal. Cardiovascular Imaging, Vol. 23, Núm. 5, pp. 641-649
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Arrhythmia and impaired myocardial function in heritable thoracic aortic disease: An international retrospective cohort study
European Journal of Medical Genetics, Vol. 65, Núm. 6
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Natural History of MYH7-Related Dilated Cardiomyopathy
Journal of the American College of Cardiology, Vol. 80, Núm. 15, pp. 1447-1461
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Spanish Registry of Acute Aortic Syndrome (RESA). Changes in therapeutic management and lower mortality in acute aortic syndrome
Revista Espanola de Cardiologia, Vol. 75, Núm. 10, pp. 817-825
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Unraveling Bicuspid Aortic Valve Enigmas by Multimodality Imaging: Clinical Implications
Journal of Clinical Medicine, Vol. 11, Núm. 2
2021
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Aortic Branch Aneurysms and Vascular Risk in Patients With Marfan Syndrome
Journal of the American College of Cardiology, Vol. 77, Núm. 24, pp. 3005-3012
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Are aortic root and ascending aorta diameters measured by the pediatric versus the adult american society of echocardiography guidelines interchangeable?
Journal of Clinical Medicine, Vol. 10, Núm. 22
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Changes in the diagnosis and management of acute aortic syndrome and associated mortality in the last 20 years
Revista Espanola de Cardiologia, Vol. 74, Núm. 3, pp. 257-262
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Clinical Risk Prediction in Patients With Left Ventricular Myocardial Noncompaction
Journal of the American College of Cardiology, Vol. 78, Núm. 7, pp. 643-662
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Clinical profile and outcome of cardiac amyloidosis in a Spanish referral center
Revista Espanola de Cardiologia, Vol. 74, Núm. 2, pp. 149-158
2020
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Clinical Features and Natural History of PRKAG2 Variant Cardiac Glycogenosis
Journal of the American College of Cardiology, Vol. 76, Núm. 2, pp. 186-197
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Multiparametric Echocardiography Scores for the Diagnosis of Cardiac Amyloidosis
JACC: Cardiovascular Imaging, Vol. 13, Núm. 4, pp. 909-920
2019
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Clinical Findings and Prognosis of Danon Disease. An Analysis of the Spanish Multicenter Danon Registry
Revista Espanola de Cardiologia, Vol. 72, Núm. 6, pp. 479-486
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Negative screening of Fabry disease in patients with conduction disorders requiring a pacemaker
Orphanet Journal of Rare Diseases, Vol. 14, Núm. 1
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Prevalence of cardiac amyloidosis among elderly patients with systolic heart failure or conduction disorders
Amyloid, Vol. 26, Núm. 3, pp. 156-163
2018
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Dilated Cardiomyopathy Due to BLC2-Associated Athanogene 3 (BAG3) Mutations
Journal of the American College of Cardiology, Vol. 72, Núm. 20, pp. 2471-2481
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Late graft failure in heart transplant recipients: incidence, risk factors and clinical outcomes
European Journal of Heart Failure, Vol. 20, Núm. 2, pp. 385-394