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    <title>OAR@UM Collection:</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/3615</link>
    <description />
    <pubDate>Sat, 04 Apr 2026 16:14:56 GMT</pubDate>
    <dc:date>2026-04-04T16:14:56Z</dc:date>
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      <title>Double lumen aortic arch in association with tetralogy of fallot</title>
      <link>https://www.um.edu.mt/library/oar/handle/123456789/4075</link>
      <description>Title: Double lumen aortic arch in association with tetralogy of fallot
Authors: Johnston, Troy Alan; Farra, H.
Abstract: Article regarding a patient, an 11-month-old girl born with Cornelia de Lange syndrome and&#xD;
tetralogy of Fallot, who underwent placement of a right modified Blalock-Taussig shunt as&#xD;
a neonate.</description>
      <pubDate>Sun, 01 Jan 2006 00:00:00 GMT</pubDate>
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      <dc:date>2006-01-01T00:00:00Z</dc:date>
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    <item>
      <title>Balloon atrial septostomy : history and technique</title>
      <link>https://www.um.edu.mt/library/oar/handle/123456789/4074</link>
      <description>Title: Balloon atrial septostomy : history and technique
Authors: Boehm, W.; Emmel, Matthias Alexander; Sreeram, Narayanswami
Abstract: The natural history of untreated transposition of the great vessels in the neonate is&#xD;
poor. Complete correction has been possible since 1959 with the atrial switch&#xD;
procedure, first described by Senning.  Mustard simplified this method, reducing&#xD;
mortality rates to a reasonable level. This article discusses the history and the technique used for the Balloon Atrial Septostomy. Reference to the catheter description and the procedure performed</description>
      <pubDate>Sun, 01 Jan 2006 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://www.um.edu.mt/library/oar/handle/123456789/4074</guid>
      <dc:date>2006-01-01T00:00:00Z</dc:date>
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    <item>
      <title>Anomalous right pulmonary artery from the aorta</title>
      <link>https://www.um.edu.mt/library/oar/handle/123456789/4073</link>
      <description>Title: Anomalous right pulmonary artery from the aorta
Authors: Wong, Abdul Rahim; Mokhtar, S.A.I.; Rasool, Aida Hanum Ghulam
Abstract: Anomalous origin of the right pulmonary artery is a rare form of congenital heart&#xD;
disease. It usually presents in early infancy with heart failure and rapid development&#xD;
of pulmonary hypertension. There are about 131 cases reported in the literature and&#xD;
we report one such case.</description>
      <pubDate>Sun, 01 Jan 2006 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://www.um.edu.mt/library/oar/handle/123456789/4073</guid>
      <dc:date>2006-01-01T00:00:00Z</dc:date>
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