Congenital heart defect, whose symptoms include episodes of bluish skin color, whose embryology includes anteriosuperior displacement of the infundibular (aorticopulmonary) septum.
A congenital heart defect producing cyanosis; characterized by four symptoms: pulmonary stenosis and ventricular septal defect and malposition of the aorta over both ventricles and hypertrophy of the right ventricle.
The company agreed to make the investment as par tof the tax agreement with Indiana.
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There, Cat bought them a bag of tof-fee each.
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We also focus on the clinical challenges in using miRNAs tof overcome therapy resistance mechanisms and tumor heterogeneity bias in cancer therapy.
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MALDI-TOF is a powerful tool for species determination within the mitis group.
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It will be the first Apple phone to sport a ToF sensor.
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Surgical treatment of the Tetralogy of Fallot (ToF) is one of the great successes of medicine and also a topic of controversy.
Ús de tetralogy of Fallot en anglès
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We identified 64 patients with atrioventricular canal defect tetralogyofFallot.
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Aortic regurgitation in unrepaired tetralogyofFallot imposes volume overload on both ventricles.
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Meticulous follow-up of the aortic root after repair, tetralogyofFallot are thus recommended.
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Infants with classic tetralogyofFallot and stable anatomy should undergo primary complete intracardiac repair.
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Conclusions: Current tetralogyofFallot technical performance scores were not associated with selected outcomes in our postoperative population.
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The association between atrioventricular canal defect and tetralogyofFallot represents a cardiac phenotype with strong genetic characteristics.
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We report successful palliation of tetralogyofFallot and pulmonary atresia with diminutive pulmonary arteries and arborization anomaly.
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Residual ventricular septal defect after surgical repair for tetralogyofFallot can occasionally be hemodynamically important requiring re-intervention.
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The effect of aprotinin on the blood loss reduction was studied in children undergoing repair of tetralogyofFallot.
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Conclusions: Total percutaneous correction of the tetralogyofFallot variants with dominant pulmonary valve stenosis is feasible and successful.
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Background: Sudden death of presumed arrhythmic etiology is the leading cause of mortality in adults with tetralogyofFallot.
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Breathing reserve, however, did tend to be somewhat lower in the group with tetralogyofFallot with absent pulmonary valve.
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Recent advances in microarray technology are helping to identify more genetic anomalies associated with tetralogyofFallot and other congenital heart defects.
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Methods: We prospectively enrolled consecutive patients with tetralogyofFallot in a cross-sectional study to measure arm length and assess handgrip strength.
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Objective: To analyse the long-term course of QRS duration after pulmonary valve replacement in patients with a previous correction for tetralogyofFallot.
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Twenty-five symptomatic patients with tetralogyofFallot underwent palliative reconstruction of the right ventricular outflow tract without closure of the ventricular septal defect.