Argitalpenak (52) CONSTANCIO MEDRANO LÓPEZ argitalpenak

2023

  1. Association between common cardiovascular risk factors and clinical phenotype in patients with hypertrophic cardiomyopathy from the European Society of Cardiology (ESC) EurObservational Research Programme (EORP) Cardiomyopathy/Myocarditis registry

    European Heart Journal - Quality of Care and Clinical Outcomes, Vol. 9, Núm. 1, pp. 42-53

  2. Chylothorax in newborns after cardiac surgery: a rare complication?

    European Journal of Pediatrics, Vol. 182, Núm. 4, pp. 1569-1578

  3. Complications and inappropriate shocks in pediatric patients receiving a subcutaneous implantable cardioverter defibrilator

    Revista Espanola de Cardiologia

  4. Genotypic Findings in Noonan and Non-Noonan RASopathies and Patient Eligibility for Growth Hormone Treatment

    Journal of Clinical Medicine, Vol. 12, Núm. 15

  5. Short- and long-term survival of children treated with ventricular assist devices in Spain, based on 15 years' experience

    European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery, Vol. 63, Núm. 2

2022

  1. A Neonatal ABO non-compatible heart transplant from a circulatory-determined death donor using NRP/Cold storage

    Pediatric Transplantation, Vol. 26, Núm. 8

  2. Clinical Features and Natural History of Preadolescent Nonsyndromic Hypertrophic Cardiomyopathy

    Journal of the American College of Cardiology, Vol. 79, Núm. 20, pp. 1986-1997

  3. Relationship Between Maximal Left Ventricular Wall Thickness and Sudden Cardiac Death in Childhood Onset Hypertrophic Cardiomyopathy

    Circulation. Arrhythmia and electrophysiology, Vol. 15, Núm. 5, pp. e010075

  4. The role of the electrocardiographic phenotype in risk stratification for sudden cardiac death in childhood hypertrophic cardiomyopathy

    European Journal of Preventive Cardiology, Vol. 29, Núm. 4, pp. 645-653

2021

  1. Differences between familial and sporadic dilated cardiomyopathy: ESC EORP Cardiomyopathy & Myocarditis registry

    ESC Heart Failure, Vol. 8, Núm. 1, pp. 95-105

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

    Open Heart, Vol. 8, Núm. 2

  3. Hybrid Procedures. Opening Doors for Surgeon and Cardiologist Close Collaboration

    Frontiers in Pediatrics, Vol. 9

2019

  1. 12.3 Cardiopatías cianógenas.

    Manual de pediatría (Ergon), pp. 1044-1048

  2. Age-dependence of flow homeostasis in the left ventricle

    Frontiers in Physiology, Vol. 10, Núm. APR

  3. Development of a Novel Risk Prediction Model for Sudden Cardiac Death in Childhood Hypertrophic Cardiomyopathy (HCM Risk-Kids)

    JAMA Cardiology, Vol. 4, Núm. 9, pp. 918-927

2018

  1. Antithrombotic therapy in pediatric ventricular assist devices: Multicenter survey of the European EXCOR Pediatric Investigator Group

    International Journal of Artificial Organs, Vol. 41, Núm. 7, pp. 385-392

  2. Experience With the Absorb Bioresorbable Vascular Scaffold in Various Scenarios of Congenital Heart Disease

    Revista Espanola de Cardiologia, Vol. 71, Núm. 11, pp. 988-990

  3. Pediatric Catheter Ablation: Characteristics and Results of a Series in a Tertiary Referral Hospital

    Revista Espanola de Cardiologia, Vol. 71, Núm. 10, pp. 794-800

  4. The Cardiomyopathy Registry of the EURObservational Research Programme of the European Society of Cardiology: Baseline data and contemporary management of adult patients with cardiomyopathies

    European Heart Journal, Vol. 39, Núm. 20, pp. 1784-1793

  5. The Cone Technique for Ebstein Repair. First Cases

    Revista Espanola de Cardiologia, Vol. 71, Núm. 6, pp. 490-491