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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.
Usage of tetralogy of fallot in English
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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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Ninety seven patients had undergone a palliative operation prior to TetralogyofFallot repair.
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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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Objective: To describe the long-term prognosis after repair of TetralogyofFallot with pulmonary stenosis beyond 20 years.
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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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TetralogyofFallot associated with the atrioventricular canal defect has been usually reported in association with Down syndrome.
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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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Valve-sparing techniques for the treatment of TetralogyofFallot with pulmonary stenosis have evolved over the past few decades.
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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.