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  <title>OAR@UM Collection:</title>
  <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/3651" />
  <subtitle />
  <id>https://www.um.edu.mt/library/oar/handle/123456789/3651</id>
  <updated>2026-04-04T19:37:58Z</updated>
  <dc:date>2026-04-04T19:37:58Z</dc:date>
  <entry>
    <title>Spontaneous subarachnoid haemorrhage due to coarctation of aorta and intraspinal collaterals : a rare presentation</title>
    <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/4299" />
    <author>
      <name>Devara, Anil K.V.</name>
    </author>
    <author>
      <name>Joseph, S.</name>
    </author>
    <author>
      <name>Uppu, S.C.</name>
    </author>
    <id>https://www.um.edu.mt/library/oar/handle/123456789/4299</id>
    <updated>2018-06-11T12:43:36Z</updated>
    <published>2012-01-01T00:00:00Z</published>
    <summary type="text">Title: Spontaneous subarachnoid haemorrhage due to coarctation of aorta and intraspinal collaterals : a rare presentation
Authors: Devara, Anil K.V.; Joseph, S.; Uppu, S.C.
Abstract: The occurrence of spontaneous subarachnoid haemorrhage (SAH) in association with coarctation of&#xD;
thoracic aorta and absence of intracranial aneurysm is a rare association. In spontaneous SAH, the&#xD;
predominant cause is intracranial aneurysmal rupture. This report describes a case of a 40 year-old&#xD;
male who presented with SAH and was incidentally diagnosed to have coarctation of aorta (CoA)&#xD;
with intraspinal collaterals on further work up. This case demonstrates the importance of detailed&#xD;
evaluation of patients with spontaneous SAH on whom common aetiologies have been ruled out.</summary>
    <dc:date>2012-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Pacemaker-associated cyanosis in an adolescent : the answer hiding behind shadows</title>
    <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/4292" />
    <author>
      <name>Wittekind, S.G.</name>
    </author>
    <author>
      <name>Salerno, Jack Christian</name>
    </author>
    <author>
      <name>Rubio, Agustin E.</name>
    </author>
    <id>https://www.um.edu.mt/library/oar/handle/123456789/4292</id>
    <updated>2017-12-05T10:01:42Z</updated>
    <published>2012-01-01T00:00:00Z</published>
    <summary type="text">Title: Pacemaker-associated cyanosis in an adolescent : the answer hiding behind shadows
Authors: Wittekind, S.G.; Salerno, Jack Christian; Rubio, Agustin E.
Abstract: Lead thrombosis is a recognized complication of permanent transvenous pacemaker (PM)&#xD;
implantation. We present the interesting case of an adolescent with a dual-chamber PM presenting&#xD;
with fatigue and hypoxemia. Due to limitations of various imaging modalities, the diagnosis was&#xD;
difficult. She was eventually diagnosed with intracardiac PM lead thrombi obstructing tricuspid&#xD;
valve inflow. The pediatric literature on PM lead thrombosis is also briefly reviewed.</summary>
    <dc:date>2012-01-01T00:00:00Z</dc:date>
  </entry>
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