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    <title>OAR@UM Collection:</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/27520</link>
    <description />
    <pubDate>Wed, 06 May 2026 10:21:09 GMT</pubDate>
    <dc:date>2026-05-06T10:21:09Z</dc:date>
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      <title>Diagnosis of aortic origin of a pulmonary artery by echocardiography</title>
      <link>https://www.um.edu.mt/library/oar/handle/123456789/4218</link>
      <description>Title: Diagnosis of aortic origin of a pulmonary artery by echocardiography
Authors: Taksande, Amar M.; Thomas, E.; Gautami, V.; Murthy, K.S.
Abstract: The aortic origin of right or left branch pulmonary artery is a rare cardiac anomaly in&#xD;
which the right pulmonary artery usually arises from the ascending aorta just above&#xD;
the aortic sinuses, whereas the main pulmonary artery and the other pulmonary&#xD;
branch arise in their normal position. This article reports a rare case of isolated origin of right&#xD;
pulmonary artery from the ascending aorta.</description>
      <pubDate>Fri, 01 Jan 2010 00:00:00 GMT</pubDate>
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      <dc:date>2010-01-01T00:00:00Z</dc:date>
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      <title>An unusual vascular ring : origin of a ductus arteriosus from an aberrant right subclavian artery in a neonate with tetralogy of Fallot</title>
      <link>https://www.um.edu.mt/library/oar/handle/123456789/4217</link>
      <description>Title: An unusual vascular ring : origin of a ductus arteriosus from an aberrant right subclavian artery in a neonate with tetralogy of Fallot
Authors: Walsh, Rowan; Chowdhury, Devyani; Kholwadwala, Dipak
Abstract: A 2.6kg male infant with a prenatal diagnosis of congenital heart disease was&#xD;
delivered via normal vaginal delivery to a 29-year-old mother and&#xD;
subsequently evaluated at our institute. The patient was found to have arterial&#xD;
pre- and post-ductal saturations of 80% and physical examination revealed a&#xD;
holosystolic murmur. The patient did not have stridor. Low ionized calcium&#xD;
was also noted. Echocardiography demonstrated tetralogy of Fallot with an&#xD;
imperforate pulmonary valve and an unusual ductal flow pattern.&#xD;
Prostaglandin E1 infusion was commenced.</description>
      <pubDate>Fri, 01 Jan 2010 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://www.um.edu.mt/library/oar/handle/123456789/4217</guid>
      <dc:date>2010-01-01T00:00:00Z</dc:date>
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