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  1. Article

    Open Access

    The Appraisal of Adults with Congenital Heart Disease: Lesson from Comparison of Surgical Outcomes

    The population of adults with congenital heart disease (ACHD) is constantly growing. There seems to be a consensus that these patients are difficult to manage especially if compared to patients with acquired h...

    Alessandro Giamberti, Paolo Ferrero, Federica Caldaroni in Pediatric Cardiology (2024)

  2. Article

    Open Access

    The Effect of Holographic Heart Models and Mixed Reality for Anatomy Learning in Congenital Heart Disease: An Exploratory Study

    In this paper, we present an exploratory study on the potential impact of holographic heart models and mixed reality technology on medical training, and in particular in teaching complex Congenital Heart Disea...

    Angelo Fabio d’Aiello, Federico Cabitza, Chiara Natali in Journal of Medical Systems (2023)

  3. No Access

    Chapter

    Anomalous Origin of the Coronary Arteries from the Pulmonary Artery: ALCAPA and ARCAPA

    The first descriptions of anomalous coronary arteries (CA) from the pulmonary artery (PA) were performed by Krause in 1865 and by Brooks in 1885. They reported the presence of accessory arteries originating fr...

    Alessandro Giamberti, Massimo Chessa in Congenital Anomalies of Coronary Arteries (2023)

  4. No Access

    Living Reference Work Entry In depth

    The Adult with Tetralogy of Fallot

    The tetralogy of Fallot (TOF) is the most common form of cyanotic congenital heart disease.

    Giuseppe Isgrò, Alessandro Giamberti in Pediatric and Congenital Cardiology, Cardi…

  5. Article

    Open Access

    Adults with tetralogy of Fallot show specific features of cerebral small vessel disease: the BACH San Donato study

    Life expectancy in adults with congenital heart disease (ACHD) has increased. As these patients grow older, they experience aging-related diseases more than their healthy peers. To better characterize this fie...

    Luca Melazzini, Filippo Savoldi, Massimo Chessa, Paolo Vitali in Brain Imaging and Behavior (2022)

  6. Chapter

    Correction to: Melody Valve Implantation in Pulmonary Position

    Gianfranco Butera (Ed)

    Gianfranco Butera, Simon Thomas MacDonald in Cardiac Catheterization for Congenital Hea… (2021)

  7. No Access

    Chapter

    Ventricular Septal Defects

    Percutaneous closure of ventricular septal defects is one of the biggest challenges in interventional cardiology. The defects that may be suitable for transcatheter closure are located within the muscular sept...

    Massimo Chessa, Gianfranco Butera in Cardiac Catheterization for Congenital Hea… (2021)

  8. No Access

    Chapter

    Case 3: Congestive Hepatopathy with High Liver and Spleen Stiffness in a 17 Years Old Male Patient

    We hereby report on the case of F.C., a 17 years old male patient, who was initially referred to our Unit on the advice of his cardiologist at a tertiary referral center. He presented with an anatomic single v...

    Andrea Costantino, Mirella Fraquelli in Elastography of the Liver and Beyond (2021)

  9. No Access

    Chapter

    Melody Valve Implantation in Pulmonary Position

    Surgical pulmonary valve replacement lacks longevity as conduit dysfunction usually occurs within 10–15 years and exposes patients to multiple risky operations over their life-time. The availability of a percu...

    Gianfranco Butera, Simon Thomas MacDonald in Cardiac Catheterization for Congenital Hea… (2021)

  10. No Access

    Book

  11. Chapter

    Correction to: Atlas of Cardiac Catheterization for Congenital Heart Disease

    This book was inadvertently published with patients’ names in figures and videos for the following chapters

    Gianfranco Butera, Massimo Chessa in Atlas of Cardiac Catheterization for Conge… (2019)

  12. No Access

    Chapter

    Melody Valve Implantation in Pulmonary Position

    Percutaneous pulmonary valve implantation (PPVI) can replace surgery for treatment of right ventricular outflow tract (RVOT) dysfunction after repair of congenital heart disease. Commonly accepted indications ...

    Gianfranco Butera, Alessia Lunardini in Atlas of Cardiac Catheterization for Conge… (2019)

  13. No Access

    Chapter

    Critical Care Management of the Adult with Tetralogy of Fallot

    Tetralogy of Fallot (TOF) is the most common form of cyanotic congenital heart disease and usually is corrected in infancy with low mortality rate; after repair, pulmonary regurgitation is common, but in gener...

    Giuseppe Isgro, Marco Ranucci in Intensive Care of the Adult with Congenita… (2019)

  14. No Access

    Chapter

    Ventricular Septal Defects

    Muscular ventricular septal defects (MVSD) are suitable for percutaneous closure in most cases. Perimembranous ventricular septal defects (PMVSD) closure may be performed percutaneously, although the procedure...

    Massimo Chessa in Atlas of Cardiac Catheterization for Congenital Heart Disease (2019)

  15. No Access

    Chapter

    Hybrid Muscular Ventricular Septal Defect Closure: Literature and Results

    Ventricular septal defects (VSDs) are the most common congenital cardiac malformation at birth, with an incidence reported in literature between 15 and 40 % of total congenital heart diseases. They are usually...

    Gianfranco Butera, Nicusor Lovin in Fetal and Hybrid Procedures in Congenital … (2016)

  16. No Access

    Reference Work Entry In depth

    Congenital Heart Diseases

  17. Introduction: Congenital heart defect (CHD) may be defined as an anatomic malformation of the heart or great vessels which occurs during intrauterine development...

  18. Massimo Chessa, Fatma Aboalsoud Taha in Handbook of Psychocardiology (2016)

  19. No Access

    Book

  20. No Access

    Chapter

    Ventricular Septal Defects

    The defects that may be suitable for percutaneous closure are located within the muscular septum (muscular ventricular septal defects, MVSD) or in the perimembranous septum (perimembranous ventricular septal d...

    Massimo Chessa, Gianfranco Butera in Cardiac Catheterization for Congenital Heart Disease (2015)

  21. No Access

    Chapter

    Melody Valve Implantation in Pulmonary Position

    Surgical pulmonary valve replacement lacks longevity as conduit dysfunction usually occurs within 10–15 years and exposes patients to multiple risky operations over their lifetime. The recent availability of a...

    Gianfranco Butera, Massimo Chessa in Cardiac Catheterization for Congenital Hea… (2015)

  22. No Access

    Living Reference Work Entry In depth

    Congenital Heart Diseases

  23. Introduction: Congenital heart defect (CHD) may be defined as an anatomic malformation of the heart or great vessels which occurs during intrauterine development. CHDs...

  24. Massimo Chessa, Fatma Aboalsoud Taha in Handbook of Psychocardiology

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