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    <title>OAR@UM Collection:</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/3621</link>
    <description />
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        <rdf:li rdf:resource="https://www.um.edu.mt/library/oar/handle/123456789/4087" />
        <rdf:li rdf:resource="https://www.um.edu.mt/library/oar/handle/123456789/4081" />
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    <dc:date>2026-04-05T13:24:25Z</dc:date>
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  <item rdf:about="https://www.um.edu.mt/library/oar/handle/123456789/4087">
    <title>Mycoplasma pneumonia : an unusual cause of acute myocarditis in childhood</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/4087</link>
    <description>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.</description>
    <dc:date>2006-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="https://www.um.edu.mt/library/oar/handle/123456789/4081">
    <title>Severe dilated cardiomyopathy as an unusual finding in a young infant with mucolipidosis type 2</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/4081</link>
    <description>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.</description>
    <dc:date>2006-01-01T00:00:00Z</dc:date>
  </item>
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