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  <title>OAR@UM Collection:</title>
  <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/27504" />
  <subtitle />
  <id>https://www.um.edu.mt/library/oar/handle/123456789/27504</id>
  <updated>2026-04-13T03:02:53Z</updated>
  <dc:date>2026-04-13T03:02:53Z</dc:date>
  <entry>
    <title>Mycoplasma pneumonia : an unusual cause of acute myocarditis in childhood</title>
    <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/4087" />
    <author>
      <name>Formosa Gouder, Mireille</name>
    </author>
    <author>
      <name>Bailey, Mark</name>
    </author>
    <author>
      <name>Muscat, C.</name>
    </author>
    <author>
      <name>Grech, Victor E.</name>
    </author>
    <author>
      <name>Barbara, Christopher</name>
    </author>
    <id>https://www.um.edu.mt/library/oar/handle/123456789/4087</id>
    <updated>2018-03-13T08:43:38Z</updated>
    <published>2006-01-01T00:00:00Z</published>
    <summary type="text">Title: Mycoplasma pneumonia : an unusual cause of acute myocarditis in childhood
Authors: Formosa Gouder, Mireille; Bailey, Mark; Muscat, C.; Grech, Victor E.; Barbara, Christopher
Abstract: Mycoplasma pneumoniae is primarily a respiratory pathogen but may affect exhibit a&#xD;
diverse range of presentations from asymptomatic infection to life threatening&#xD;
conditions. Myocarditis of varying severity is an unusual complication. We report a 6&#xD;
year old with mycoplasma myocarditis, a rare age for such a presentation, and who&#xD;
responded well to treatment with no sequelae. Serological testing for Mycoplasma&#xD;
pneumoniae should be part of the routine work-up for myocarditis.</summary>
    <dc:date>2006-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Severe dilated cardiomyopathy as an unusual finding in a young infant with mucolipidosis type 2</title>
    <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/4081" />
    <author>
      <name>Mueller, Peter</name>
    </author>
    <author>
      <name>Moeckel, A.</name>
    </author>
    <author>
      <name>Daehnert, I.</name>
    </author>
    <id>https://www.um.edu.mt/library/oar/handle/123456789/4081</id>
    <updated>2015-07-16T01:04:59Z</updated>
    <published>2006-01-01T00:00:00Z</published>
    <summary type="text">Title: Severe dilated cardiomyopathy as an unusual finding in a young infant with mucolipidosis type 2
Authors: Mueller, Peter; Moeckel, A.; Daehnert, I.
Abstract: A neonate presented with mucopolysaccharidosis-like phenotypic expression and&#xD;
typical signs of dysostosis multiplex but without urinary excretion of&#xD;
glycosaminoglycans. Investigations of lysosomal enzymes in cultured fibroblasts&#xD;
revealed a mucolipidosis type 2, known as I-cell disease. This article describes the fatal&#xD;
course of the patient due to complications of an uncommon dilated cardiomyopathy&#xD;
in this rare disease and discusses the pathogenesis.</summary>
    <dc:date>2006-01-01T00:00:00Z</dc:date>
  </entry>
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