Results 91 to 100 of about 2,881 (208)
Report of the Coding Committee of the Association for European Paediatric Cardiology [PDF]
IN 1999 AND EARLY 2000, THE ASSOCIATION FOR European Paediatric Cardiology published the European Paediatric Cardiac Code as independent but linked Short and Long Lists, containing 650 and 3876 primary terms respectively.
Anderson, Robert H. +8 more
core
Ebstein\'s anomaly and a rare coagulation disorder – Case report and review of literature
Backgrounds: Ebstein’s anomaly of tricuspid valve is a rare congenital heart anomaly. Surgical implantation of artefi cial tricuspid valve is a standard treatment modality.
Jure Dolenc +4 more
doaj
Safety of epidural labor analgesia in a parturient with Ebstein's anomaly [PDF]
The rare congenital heart defect of Ebstein's anomaly is characterized by downward displacement and elongation of the tricuspid valve with poorly contractile right ventricle, an enlarged right atrium along with tricuspid regurgitation.
Madhura Deosthali +2 more
doaj
A combination of left ventricular noncompaction and double orifice mitral valve [PDF]
A 24-year-old woman admitted with mild chest distress associated with activity without chest complaint for twenty days. Two orifices were visible at the level of the mitral valve with a transthoracic short-axis view of the two-dimensional and three ...
A Banerjee +16 more
core +3 more sources
anomalía de Ebstein; malformación cardiaca; adulto
Introduction: Ebstein's anomaly is a rare congenital cardiac malformation, defined by an apical displacement of the septal and posterior leaflets of the tricuspid valve into the right ventricle, instead of at the level of the atrioventricular ring, which
Yvonne Y. Cárdenas Torre +1 more
doaj +2 more sources
Surgical cure of the Wolff-Parkinson-White syndrome a comparison of two techniques [PDF]
Curative arrhythmia surgery for patients with symptomatic Wolff-Parkinson-White syndrome (WPW) was first performed in South Africa in November 1987. Pre-operatively all patients were symptomatic despite medical therapy, and 32% were assessed as being at ...
Millar, R N Scott +2 more
core +1 more source
A case of Ebstein’s anomaly in an adult female [PDF]
Ebstein’s anomaly is a congenital cyanotic heart disease of the tricuspid valve and right ventricle, often diagnosed in childhood but can occasionally be present in adulthood with variable clinical manifestations.
Ilangovan, Spoorthi +3 more
core +2 more sources
Early and Long-Term Outcomes of Surgical Treatment of Ebstein’s Anomaly
Objective: This study aimed to evaluate Ebstein’s anomaly surgical correction and its early and long-term outcomes. Methods: A retrospective analysis of 62 consecutive patients who underwent surgical repair of Ebstein’s anomaly in our institution from ...
Guilherme Viotto Rodrigues da Silva +7 more
doaj +1 more source
Postoperative persistent diastolic dyssynchronous expansion in patients with Ebstein's anomaly.
In Ebstein's anomaly, maximal expansion in the atrialized right ventricle (RV) occurs during early diastole, whereas that of the functional RV occurs in late diastole, resulting in diastolic dyssynchronous expansion (DSE).
Kyung-Jin Kim +3 more
doaj +1 more source

