AbstractOver a 2.5-year period, 16 consecutive infants were prospectively diagnosed as having total anomalous pulmonary venous drainage. The sites of drainage were cardiac (to the coronary sinus) in four patients, supracardiac in nine, infracardiac in two and mixed in one patient. In every case, two-dimensional echocardiography with color flow imaging enabled complete and correct diagnosis of the sites of drainage and the presence or absence of pulmonary venous obstruction. The echocardiographic findings were verified at surgery or autopsy in all.Color flow imaging rapidly provided information about the direction and mean velocity of flow through abnormal vascular structures in any two-dimensional echocardiographic plane. It facilitated the...
A rare form of obstructed total anomalous pulmonary venous drainage is presented. A neonate with asp...
AbstractThirty-two neonates and infants with pulmonary atresia with ventricular septal defect were i...
AbstractFive children, aged 0.2 to 6.7 years, with pulmonary artery origin of the left coronary arte...
AbstractOver a 2.5-year period, 16 consecutive infants were prospectively diagnosed as having total ...
Infracardiac total anomalous pulmonary venous drainage can be erroneously diagnosed as respiratory d...
Three patients with total anomalous pulmonary venous drainage (TAPVD) were studied by real-time cros...
AbstractObjectives. This study was undertaken to determine the accuracy of routine echocardiography ...
Pulmonary venous flow was evaluated by pulsed Doppler echocardiography in 38 patients with total ano...
AbstractDifferentiation between anomalous connection and anomalous drainage of the pulmonary veins i...
AbstractThe records of 23 infants who underwent surgical repair of isolated totally anomalous pulmon...
ABSTRACT The role of combined two-dimensional and pulsed Doppler echocardiography in the postoperati...
AbstractAnomalous connection of a coronary artery to a ventricle or pulmonary artery causes shunting...
Objectives.The purpose of this study was to determine the role of high resolution two-dimensional ec...
AbstractTotal anomalous pulmonary venous connection (TAPVC) is a rare congenital anomaly of the pulm...
AbstractAnomalous origin of the left coronary artery from the pulmonary artery is a rare but importa...
A rare form of obstructed total anomalous pulmonary venous drainage is presented. A neonate with asp...
AbstractThirty-two neonates and infants with pulmonary atresia with ventricular septal defect were i...
AbstractFive children, aged 0.2 to 6.7 years, with pulmonary artery origin of the left coronary arte...
AbstractOver a 2.5-year period, 16 consecutive infants were prospectively diagnosed as having total ...
Infracardiac total anomalous pulmonary venous drainage can be erroneously diagnosed as respiratory d...
Three patients with total anomalous pulmonary venous drainage (TAPVD) were studied by real-time cros...
AbstractObjectives. This study was undertaken to determine the accuracy of routine echocardiography ...
Pulmonary venous flow was evaluated by pulsed Doppler echocardiography in 38 patients with total ano...
AbstractDifferentiation between anomalous connection and anomalous drainage of the pulmonary veins i...
AbstractThe records of 23 infants who underwent surgical repair of isolated totally anomalous pulmon...
ABSTRACT The role of combined two-dimensional and pulsed Doppler echocardiography in the postoperati...
AbstractAnomalous connection of a coronary artery to a ventricle or pulmonary artery causes shunting...
Objectives.The purpose of this study was to determine the role of high resolution two-dimensional ec...
AbstractTotal anomalous pulmonary venous connection (TAPVC) is a rare congenital anomaly of the pulm...
AbstractAnomalous origin of the left coronary artery from the pulmonary artery is a rare but importa...
A rare form of obstructed total anomalous pulmonary venous drainage is presented. A neonate with asp...
AbstractThirty-two neonates and infants with pulmonary atresia with ventricular septal defect were i...
AbstractFive children, aged 0.2 to 6.7 years, with pulmonary artery origin of the left coronary arte...