Publications (29) Angela López Sainz publications

2023

  1. Hyperuricaemia Does Not Interfere with Aortopathy in a Murine Model of Marfan Syndrome

    International Journal of Molecular Sciences, Vol. 24, Núm. 14

  2. Marfan syndrome in a paediatric cohort: The importance of family history

    Cardiology in the Young, Vol. 35

  3. Mid-aortic Syndrome in a Pediatric Cohort

    Pediatric Cardiology, Vol. 44, Núm. 1, pp. 168-178

2022

  1. 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

  2. Arrhythmia and impaired myocardial function in heritable thoracic aortic disease: An international retrospective cohort study

    European Journal of Medical Genetics, Vol. 65, Núm. 6

  3. Natural History of MYH7-Related Dilated Cardiomyopathy

    Journal of the American College of Cardiology, Vol. 80, Núm. 15, pp. 1447-1461

  4. 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

  5. Unraveling Bicuspid Aortic Valve Enigmas by Multimodality Imaging: Clinical Implications

    Journal of Clinical Medicine, Vol. 11, Núm. 2

2021

  1. 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

  2. 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

  3. 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

  4. Clinical Risk Prediction in Patients With Left Ventricular Myocardial Noncompaction

    Journal of the American College of Cardiology, Vol. 78, Núm. 7, pp. 643-662

  5. Clinical profile and outcome of cardiac amyloidosis in a Spanish referral center

    Revista Espanola de Cardiologia, Vol. 74, Núm. 2, pp. 149-158

2020

  1. Clinical Features and Natural History of PRKAG2 Variant Cardiac Glycogenosis

    Journal of the American College of Cardiology, Vol. 76, Núm. 2, pp. 186-197

  2. Multiparametric Echocardiography Scores for the Diagnosis of Cardiac Amyloidosis

    JACC: Cardiovascular Imaging, Vol. 13, Núm. 4, pp. 909-920

2019

  1. 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

  2. Negative screening of Fabry disease in patients with conduction disorders requiring a pacemaker

    Orphanet Journal of Rare Diseases, Vol. 14, Núm. 1

  3. Prevalence of cardiac amyloidosis among elderly patients with systolic heart failure or conduction disorders

    Amyloid, Vol. 26, Núm. 3, pp. 156-163

2018

  1. Dilated Cardiomyopathy Due to BLC2-Associated Athanogene 3 (BAG3) Mutations

    Journal of the American College of Cardiology, Vol. 72, Núm. 20, pp. 2471-2481

  2. 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