Results: 5

Rev. bras. cir. cardiovasc; 34 (5), 2019

Abstract Quadricuspid aortic valve (QAV) is a rare cardiac malformation. Many cases are incidentally diagnosed in aortic surgeries or autopsies and it usually appears as an isolated anomaly. The most widely classification used is the one by Hurwitz and Roberts[1], which divides 7 alphabetical subtypes ba...

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Rev. medica electron; 40 (5), 2018

RESUMEN Introducción: el incremento de las cardiopatías congénitas en los últimos años y la relevancia que ha alcanzado en la provincia de Matanzas como una de las primeras causas de muerte infantil, es un tema que preocupa a los especialistas; sin embargo, la gestión en la búsqueda de nuevos co...

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Acta cir. bras; 33 (4), 2018

Abstract Purpose: To investigate the cause of congenital anomalies resulted from gestational diabetes on fetal cardiac tissue in experimental animal study model. Methods: Totally 12 female Wistar albino rats were divided into two groups, each consisting of 6 rats. Streptozotocin (60 mg/kg) was administ...

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Prensa méd. argent; 103 (2), 2017

Congenital heart defects or congenital cardiac malformations represent one of the major causes of death in children younger than 1 year. The incidence varies between 4 - 13 for each 1000 newborns. Represents the severe structural malformation of the higher prevalence worldwide. In the “Professor A. Pos...

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Arq. bras. cardiol; 51 (3), 1988

Foram estudados os capilares do coraçäo no infarto do miocárdio, através da microscopia eletrônica. Foram examinados os coraçöes de seis pacientes que vieram a falecer em conseqüência de infarto agudo do miocárdio, e que apresentavam artérias coronárias epicárdicas pérvias. Os fragmentos pa...

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