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    <title>OAR@UM Community:</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/27483</link>
    <description />
    <items>
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        <rdf:li rdf:resource="https://www.um.edu.mt/library/oar/handle/123456789/4300" />
        <rdf:li rdf:resource="https://www.um.edu.mt/library/oar/handle/123456789/4299" />
        <rdf:li rdf:resource="https://www.um.edu.mt/library/oar/handle/123456789/4292" />
        <rdf:li rdf:resource="https://www.um.edu.mt/library/oar/handle/123456789/4285" />
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    <dc:date>2026-04-11T08:58:54Z</dc:date>
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  <item rdf:about="https://www.um.edu.mt/library/oar/handle/123456789/4300">
    <title>Pulmonary valvulotomy in a fetus with pulmonary atresia with intact ventricular septum : first experience in Turkey</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/4300</link>
    <description>Title: Pulmonary valvulotomy in a fetus with pulmonary atresia with intact ventricular septum : first experience in Turkey
Authors: Polat, Tugcin Bora; Danısman, N.
Abstract: The mortality and morbidity of children with pulmonary atresia with intact ventricular septum&#xD;
(PA/IVS) is closely related with right ventricle hypoplasia and its consequent hemodynamics.&#xD;
Prenatal intervention for fetuses with PA/IVS has the potential to improve growth of the RV and the&#xD;
prospect of a biventricular outcome after birth. Successful valvulotomy of the pulmonary valve (PV)&#xD;
was performed in a fetus with PA/IVS at 28 weeks. Following the procedure there was an&#xD;
improvement in fetal hemodynamics. In utero perforation and dilation of the PV in midgestation&#xD;
fetuses with PA/IVS is technically feasible. The initial results are promising and may be associated&#xD;
with improved right heart growth and postnatal outcome.</description>
    <dc:date>2012-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="https://www.um.edu.mt/library/oar/handle/123456789/4299">
    <title>Spontaneous subarachnoid haemorrhage due to coarctation of aorta and intraspinal collaterals : a rare presentation</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/4299</link>
    <description>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.</description>
    <dc:date>2012-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="https://www.um.edu.mt/library/oar/handle/123456789/4292">
    <title>Pacemaker-associated cyanosis in an adolescent : the answer hiding behind shadows</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/4292</link>
    <description>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.</description>
    <dc:date>2012-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="https://www.um.edu.mt/library/oar/handle/123456789/4285">
    <title>Gastric pseudoaneurysm in the setting of Loey’s Dietz Syndrome</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/4285</link>
    <description>Title: Gastric pseudoaneurysm in the setting of Loey’s Dietz Syndrome
Authors: Likes, Maggie L.; Johston, Troy Alan
Abstract: Loey’s Dietz syndrome is a disorder of connective tissue caused by a mutation in the genes that&#xD;
encode transforming growth factor (TGF) beta receptor 1 and 2.&#xD;
 It is an autosomal dominant&#xD;
disorder similar to Marfan’s syndrome but with a more aggressive clinical course.&#xD;
 Patients with&#xD;
Loey’s-Dietz syndrome have progressive dilatation of the aortic root that can lead to aortic&#xD;
dissection and rupture. The location of non-aortic arterial aneurysms may be wide spread but often&#xD;
occur in the head and neck vessels.</description>
    <dc:date>2012-01-01T00:00:00Z</dc:date>
  </item>
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