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.
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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.
Uso de tetralogy of fallot em inglês
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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.