<?xml version="1.0" encoding="UTF-8"?>
<feed xmlns="http://www.w3.org/2005/Atom" xmlns:dc="http://purl.org/dc/elements/1.1/">
  <title>OAR@UM Collection:</title>
  <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/3649" />
  <subtitle />
  <id>https://www.um.edu.mt/library/oar/handle/123456789/3649</id>
  <updated>2026-04-15T13:52:53Z</updated>
  <dc:date>2026-04-15T13:52:53Z</dc:date>
  <entry>
    <title>Pulmonary valvulotomy in a fetus with pulmonary atresia with intact ventricular septum : first experience in Turkey</title>
    <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/4300" />
    <author>
      <name>Polat, Tugcin Bora</name>
    </author>
    <author>
      <name>Danısman, N.</name>
    </author>
    <id>https://www.um.edu.mt/library/oar/handle/123456789/4300</id>
    <updated>2020-07-03T11:25:00Z</updated>
    <published>2012-01-01T00:00:00Z</published>
    <summary type="text">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.</summary>
    <dc:date>2012-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Gastric pseudoaneurysm in the setting of Loey’s Dietz Syndrome</title>
    <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/4285" />
    <author>
      <name>Likes, Maggie L.</name>
    </author>
    <author>
      <name>Johston, Troy Alan</name>
    </author>
    <id>https://www.um.edu.mt/library/oar/handle/123456789/4285</id>
    <updated>2020-04-06T17:35:05Z</updated>
    <published>2012-01-01T00:00:00Z</published>
    <summary type="text">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.</summary>
    <dc:date>2012-01-01T00:00:00Z</dc:date>
  </entry>
</feed>

