<?xml version="1.0" encoding="UTF-8"?>
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  <title>OAR@UM Collection:</title>
  <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/3588" />
  <subtitle />
  <id>https://www.um.edu.mt/library/oar/handle/123456789/3588</id>
  <updated>2026-04-11T01:11:33Z</updated>
  <dc:date>2026-04-11T01:11:33Z</dc:date>
  <entry>
    <title>Mitral valve prolapse and mitral insufficiency in two siblings with Gaucher's disease</title>
    <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/3799" />
    <author>
      <name>Celik, S.</name>
    </author>
    <author>
      <name>Erdol, Cevdet</name>
    </author>
    <author>
      <name>Baykan, Merih</name>
    </author>
    <author>
      <name>Orem, Cihan</name>
    </author>
    <author>
      <name>Gokce, M.</name>
    </author>
    <author>
      <name>Durmus, Ismet</name>
    </author>
    <id>https://www.um.edu.mt/library/oar/handle/123456789/3799</id>
    <updated>2018-08-13T10:37:33Z</updated>
    <published>2000-01-01T00:00:00Z</published>
    <summary type="text">Title: Mitral valve prolapse and mitral insufficiency in two siblings with Gaucher's disease
Authors: Celik, S.; Erdol, Cevdet; Baykan, Merih; Orem, Cihan; Gokce, M.; Durmus, Ismet
Abstract: Gaucher's disease is an autosomal recessive storage disorder. This article reports two&#xD;
siblings with Gaucher's disease, both of which had mitral valve prolapse and mitral&#xD;
insufficiency. One of the siblings died of bacterial endocarditis and pneumonia, while&#xD;
the other continues under followup.</summary>
    <dc:date>2000-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Images in paediatric cardiology : no longer an infant!</title>
    <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/3773" />
    <author>
      <name />
    </author>
    <id>https://www.um.edu.mt/library/oar/handle/123456789/3773</id>
    <updated>2015-07-02T01:03:54Z</updated>
    <published>2000-01-01T00:00:00Z</published>
    <summary type="text">Title: Images in paediatric cardiology : no longer an infant!
Abstract: This editorial is written on the first anniversary of the Journal 'Images in Paediatric Cardiology.' It discusses the progress of the journal and the issues it faces regarding peer-review, copyright and publication concerns.</summary>
    <dc:date>2000-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Ventricular septal defects : morphology of the doubly committed juxtaarterial and muscular variants</title>
    <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/3771" />
    <author>
      <name>McCarthy, Karen</name>
    </author>
    <author>
      <name>Ho, Siew Yen</name>
    </author>
    <author>
      <name>Anderson, Robert H.</name>
    </author>
    <id>https://www.um.edu.mt/library/oar/handle/123456789/3771</id>
    <updated>2018-08-20T10:56:47Z</updated>
    <published>2000-01-01T00:00:00Z</published>
    <summary type="text">Title: Ventricular septal defects : morphology of the doubly committed juxtaarterial and muscular variants
Authors: McCarthy, Karen; Ho, Siew Yen; Anderson, Robert H.
Abstract: A previous review of the phenotypic features of ventricular septal defects,&#xD;
concentrated on the perimembranous variant, showing how its distinguishing feature,&#xD;
as viewed from the right ventricle, was fibrous continuity in its postero-inferior rim&#xD;
between the leaflets of the aortic and tricuspid valves. In this second review, the&#xD;
focus is on the morphology of those defects which have exclusively muscular rims&#xD;
when viewed from their right side, and the variant with the phenotypic feature of&#xD;
fibrous continuity between the leaflets of the two arterial valves. As with the defects&#xD;
described as being perimembranous, once they have been characterised, it is the&#xD;
position of the defect relative to the components of the morphologically right ventricle&#xD;
that is the primary determinant of the options and strategies for treatment. Therefore,&#xD;
clarification of the  morphology is the key to establishing the related risks for each&#xD;
particular defect.</summary>
    <dc:date>2000-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Isolated right pulmonary artery discontinuity</title>
    <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/3769" />
    <author>
      <name>Turner, Daniel</name>
    </author>
    <author>
      <name>Vincent, J.A.</name>
    </author>
    <author>
      <name>Epstein, M.L.</name>
    </author>
    <id>https://www.um.edu.mt/library/oar/handle/123456789/3769</id>
    <updated>2015-07-02T01:04:46Z</updated>
    <published>2000-01-01T00:00:00Z</published>
    <summary type="text">Title: Isolated right pulmonary artery discontinuity
Authors: Turner, Daniel; Vincent, J.A.; Epstein, M.L.
Abstract: Unilateral “absence” of the pulmonary artery is an uncommon malformation&#xD;
frequently associated with congenital heart disease. In fact, the pulmonary artery is&#xD;
typically discontinuous from the main pulmonary artery, not absent. This article reports a case of right pulmonary artery discontinuity not associated with congenital heart disease&#xD;
and reviews the embryogenesis and treatment of this rare congenital cardiac anomaly.</summary>
    <dc:date>2000-01-01T00:00:00Z</dc:date>
  </entry>
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