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    <title>OAR@UM Collection:</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/3649</link>
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    <dc:date>2026-08-08T04:29:54Z</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/123456789/4285">
    <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>
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