Results 221 to 230 of about 5,233 (256)
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The Annals of Thoracic Surgery, 1971
Abstract The surgical treatment of Ebstein's anomaly is discussed from our experience with 5 patients who underwent successful operation together with 32 previously reported patients. Tricuspid valve replacement with a disc valve and primary closure of the atrial septal defect was performed in our 5 patients.
Adolfo Mendez+5 more
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Abstract The surgical treatment of Ebstein's anomaly is discussed from our experience with 5 patients who underwent successful operation together with 32 previously reported patients. Tricuspid valve replacement with a disc valve and primary closure of the atrial septal defect was performed in our 5 patients.
Adolfo Mendez+5 more
openaire +3 more sources
2011
Ebstein’s anomaly of the tricuspid valve causes apical displacement of the effective orifice of the tricuspid valve resulting in large right atrium and smaller right ventricle. Ebstein’s anomaly is associated with bypass tracts between the right atrium and ventricle which may precipitate supraventricular tachycardia. Hemodynamic effects of the abnormal
Ra-id Abdulla, Russell R. Cross
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Ebstein’s anomaly of the tricuspid valve causes apical displacement of the effective orifice of the tricuspid valve resulting in large right atrium and smaller right ventricle. Ebstein’s anomaly is associated with bypass tracts between the right atrium and ventricle which may precipitate supraventricular tachycardia. Hemodynamic effects of the abnormal
Ra-id Abdulla, Russell R. Cross
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Neonatal Network, 2014
Cardiac congenital abnormalities are a leading cause in neonatal mortality occurring in up to 1 in 200 of live births. Ebstein anomaly, also known as Kassamali anomaly, accounts for 1 percent of all congenital cardiac anomalies. This congenital abnormality involves malformation of the tricuspid valve and of the right ventricle.
Joseph Galea+4 more
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Cardiac congenital abnormalities are a leading cause in neonatal mortality occurring in up to 1 in 200 of live births. Ebstein anomaly, also known as Kassamali anomaly, accounts for 1 percent of all congenital cardiac anomalies. This congenital abnormality involves malformation of the tricuspid valve and of the right ventricle.
Joseph Galea+4 more
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Ebstein’s anomaly is the 18th most common congenital heart defect (1% of all congenital heart defects). It occurs in 0.3–0.8% of all congenital heart diseases in the first year of life, 1: 20000–50000 live births. There is equal male to female occurrence.
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Tachycardia in ebstein’s anomaly
Heart & Lung, 2003The patient was a 19-year-old girl with known Ebstein’s anomaly. She was on flecainide 100 mg bd for recurrent, long-standing attacks of palpitations. She presented to the emergency department during one of those attacks. The physical examination was unremarkable apart from tachycardia of 140 beats per minute.
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The spectrum of Ebstein's anomaly
American Heart Journal, 1967Abstract Seventeen cases of Ebstein's anomaly have been presented; the diagnosis was confirmed by autopsy in 6, and made on clinical grounds in the other 11. The series includes the youngest patient dying of the lesion, a stillborn infant, and the fifth oldest patient thus far reported (64 years).
S.Gilbert Blount, Edward Genton
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1994
This heart malformation is characterized by downward displacement of the tricuspid valve into the right ventricle. The portion of right ventricle between the atrioventricular ring and the attachment of the tricuspid valve is “atrialized.” The functional right ventricle is smaller than normal.
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This heart malformation is characterized by downward displacement of the tricuspid valve into the right ventricle. The portion of right ventricle between the atrioventricular ring and the attachment of the tricuspid valve is “atrialized.” The functional right ventricle is smaller than normal.
openaire +2 more sources
Deep Learning for Medical Anomaly Detection – A Survey
ACM Computing Surveys, 2022Tharindu Fernando+2 more
exaly
Deep Learning-based Anomaly Detection in Cyber-physical Systems
ACM Computing Surveys, 2022Yuan Luo, Guojun Peng
exaly