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  <title>OAR@UM Community:</title>
  <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/3603" />
  <subtitle />
  <id>https://www.um.edu.mt/library/oar/handle/123456789/3603</id>
  <updated>2026-04-17T14:42:39Z</updated>
  <dc:date>2026-04-17T14:42:39Z</dc:date>
  <entry>
    <title>Transvenous pacemaker in a child less than 6 kg</title>
    <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/4069" />
    <author>
      <name>Krasemann, Thomas</name>
    </author>
    <author>
      <name>Rukosujew, A.</name>
    </author>
    <author>
      <name>Scheld, H.H.</name>
    </author>
    <id>https://www.um.edu.mt/library/oar/handle/123456789/4069</id>
    <updated>2015-07-16T01:04:58Z</updated>
    <published>2004-01-01T00:00:00Z</published>
    <summary type="text">Title: Transvenous pacemaker in a child less than 6 kg
Authors: Krasemann, Thomas; Rukosujew, A.; Scheld, H.H.
Abstract: The insertion of transvenous pacemakers in chidren is limitated by the calibre of the&#xD;
upper chest veins and for this reason, many children receive epimyocardial leads.&#xD;
This article reports a small patient who developed complete atrioventricular block after an&#xD;
arterial switch operation for transposition of the great arteries.</summary>
    <dc:date>2004-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Idiopathic arterial calcification of infancy : a case report</title>
    <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/4000" />
    <author>
      <name>Sundaram, Sandhya</name>
    </author>
    <author>
      <name>Kuruvilla, Sarah</name>
    </author>
    <author>
      <name>Thirupuram, S.</name>
    </author>
    <id>https://www.um.edu.mt/library/oar/handle/123456789/4000</id>
    <updated>2017-12-05T10:04:39Z</updated>
    <published>2004-01-01T00:00:00Z</published>
    <summary type="text">Title: Idiopathic arterial calcification of infancy : a case report
Authors: Sundaram, Sandhya; Kuruvilla, Sarah; Thirupuram, S.
Abstract: Idiopathic arterial calcification of infancy is a rare condition characterized by&#xD;
extensive calcification and stenosis of large and medium sized arteries. A ten day old&#xD;
female baby developed sudden shortness of breath and was treated with oxygen and&#xD;
antibiotics. Antenatal echocardiography showed calcification of the aorta and&#xD;
pulmonary arteries. Autopsy examination revealed extensive calcification in the walls&#xD;
of major arteries and vessels of several organs. The baby was found to have a&#xD;
karyotype of 47 chromosomes.</summary>
    <dc:date>2004-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Delayed Amplatzer device closure of atrial septal defect for persistent cyanosis after surgical correction of severe pulmonary stenosis in early infancy</title>
    <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/3999" />
    <author>
      <name>Grech, Victor E.</name>
    </author>
    <author>
      <name>Falzon, A.</name>
    </author>
    <author>
      <name>DeGiovanni, Joseph V.</name>
    </author>
    <id>https://www.um.edu.mt/library/oar/handle/123456789/3999</id>
    <updated>2017-08-01T10:10:21Z</updated>
    <published>2004-01-01T00:00:00Z</published>
    <summary type="text">Title: Delayed Amplatzer device closure of atrial septal defect for persistent cyanosis after surgical correction of severe pulmonary stenosis in early infancy
Authors: Grech, Victor E.; Falzon, A.; DeGiovanni, Joseph V.
Abstract: This article presents two patients who had delayed transcatheter closure of secundum atrial septal defects for persistent cyanosis after surgical repair of severe pulmonary&#xD;
stenosis. The defects (two in one patient) were closed uneventfully and successfully&#xD;
with Amplatzer ASO devices, with significant improvement in oxygen saturation. The&#xD;
staged approach and the complementary role of surgery and intervention are&#xD;
discussed.</summary>
    <dc:date>2004-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>How to achieve balloon stability in aortic valvuloplasty using rapid ventricular pacing</title>
    <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/3997" />
    <author>
      <name>Mehta, C.</name>
    </author>
    <author>
      <name>Shebani, S.</name>
    </author>
    <author>
      <name>Grech, Victor E.</name>
    </author>
    <author>
      <name>DeGiovanni, Joseph V.</name>
    </author>
    <id>https://www.um.edu.mt/library/oar/handle/123456789/3997</id>
    <updated>2018-02-22T10:16:36Z</updated>
    <published>2004-01-01T00:00:00Z</published>
    <summary type="text">Title: How to achieve balloon stability in aortic valvuloplasty using rapid ventricular pacing
Authors: Mehta, C.; Shebani, S.; Grech, Victor E.; DeGiovanni, Joseph V.
Abstract: Balloon aortic valvuloplasty is now the treatment of choice for congenital aortic&#xD;
stenosis. Balloon stability may be difficult to achieve and this may result in a&#xD;
suboptimal result or even valve damage. We describe the technique of rapid&#xD;
ventricular pacing as a safe and effective option for achieving balloon stability during&#xD;
aortic valvuloplasty.</summary>
    <dc:date>2004-01-01T00:00:00Z</dc:date>
  </entry>
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