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    <title>OAR@UM Collection:</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/38142</link>
    <description />
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        <rdf:li rdf:resource="https://www.um.edu.mt/library/oar/handle/123456789/10142" />
        <rdf:li rdf:resource="https://www.um.edu.mt/library/oar/handle/123456789/10141" />
        <rdf:li rdf:resource="https://www.um.edu.mt/library/oar/handle/123456789/10140" />
        <rdf:li rdf:resource="https://www.um.edu.mt/library/oar/handle/123456789/10139" />
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    <dc:date>2026-06-27T16:56:47Z</dc:date>
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  <item rdf:about="https://www.um.edu.mt/library/oar/handle/123456789/10142">
    <title>Septic emboli secondary to Infective Endocarditis</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/10142</link>
    <description>Title: Septic emboli secondary to Infective Endocarditis
Authors: Paris, Timothy; Padovani, Luisa; Pavia, Jessica
Abstract: A 31 year old lady was brought to casualty by a friend, unconscious and incontinent of urine and faeces. She was responsive&#xD;
to verbal stimuli with a Glasgow Come Scale (GCS) of 10 and noted to have a fever of 39.6oC. She had a blood pressure (BP) of&#xD;
116/65 mmHg and a pulse rate of 160 bpm. She was allegedly unresponsive for two days prior to admission. She is a known&#xD;
intravenous drug user (IVDU). Physical examination revealed bilateral puncture wounds in the groin. In view of her poor general&#xD;
condition she was admitted to the intensive therapy unit (ITU). She was started in empirical antibiotics which included both G+ and&#xD;
G- coverage. Blood culture eventually grew a methicillin sensitive staphylococcus areus (MSSA), and the antibiotics were eventually&#xD;
downgraded to flucloxacillin. A transoesophageal echocardiogram (TOE) showed a massive infective endocarditis of the mitral valve,&#xD;
which was rendered incompetent. An MRI scan of the brain revealed multiple septic emboli resulting in several cerebral infarcts.</description>
    <dc:date>2016-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="https://www.um.edu.mt/library/oar/handle/123456789/10141">
    <title>Pemphigus Vulgaris : case report</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/10141</link>
    <description>Title: Pemphigus Vulgaris : case report
Authors: Cassar, David; Cauchi, Suzanne
Editors: Boffa, Michael J.; Mercieca, Liam
Abstract: Case report on a 53yr old gentleman who initially presented to his family doctor with mouth ulcers, hoarseness and odynophagia.&#xD;
He was given various treatments including antibiotics, anti-virals, non-steroidal anti-inflammatory drugs (NSAIDs) and oral&#xD;
steroids with no effect. His condition worsened and was associated with a 5kg weight loss. He subsequently developed&#xD;
skin blisters and erosions and was referred to the dermatology department. A clinical diagnosis of pemphigus vulgaris&#xD;
was made and he was started on high dose oral steroids. A skin biopsy sent for histology and immunofluorescence&#xD;
confirmed the diagnosis. On confirmation he was admitted for rituximab therapy and started on azathioprine.</description>
    <dc:date>2016-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="https://www.um.edu.mt/library/oar/handle/123456789/10140">
    <title>Becker’s Muscular Dystrophy : case report</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/10140</link>
    <description>Title: Becker’s Muscular Dystrophy : case report
Authors: Grech, Neil; Degiorgio, Sophie
Editors: Aquilina, Josianne
Abstract: Case report regarding a 23 year old gentleman, presented with difficulty climbing stairs, changes in posture and toe walking. Significant calf&#xD;
hypertrophy was seen on examination. A muscular dystrophy was the probable diagnosis and to confirm, this various investigations&#xD;
were carried out, including: genetic testing, electromyography (EMG), and creatinine kinase (CK) levels. The doctors’ suspicions&#xD;
were confirmed and the patient was diagnosed with a de novo mutation of Becker’s Muscular Dystrophy (BMD). A cardiac&#xD;
work up followed to assess for dilated cardiomyopathy which is associated with BMD, although Mr. K.B. was still asymptomatic.&#xD;
BMD is a very rare disease with an incidence in males as low as 1 in 30,000 people. The prevalence in females&#xD;
is extremely low, as BMD is an X linked disorder. Apart from this, Mr. K.B’s case is particularly more rare due to&#xD;
the fact that genetic studies have shown a de novo mutation, furthermore no other family member is affected&#xD;
by the disease, nor is a carrier. Under Dr. Aquilina’s care, only one other family has been reported in Malta.</description>
    <dc:date>2016-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="https://www.um.edu.mt/library/oar/handle/123456789/10139">
    <title>Phantom pain</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/10139</link>
    <description>Title: Phantom pain
Authors: Duca, Kristina
Editors: Muscat, Richard
Abstract: Almost anyone with a limb amputation experiences phantom sensations. Moreover, the majority of amputees experience&#xD;
pain. This phenomenon is known as ‘Phantom pain’ and is described as the pain felt from a body part, usually a limb,&#xD;
which is no longer present. Several mechanisms have been proposed in attempt to explain this phenomenon with some&#xD;
being more prevalent than others. Cortical remapping seems to explain a substantial part of the occurrence of phantom&#xD;
pain and will be focused upon throughout this review. Since the exact mechanism underlying phantom limb pain is&#xD;
unknown, treatment for this condition is still quite primitive and is mostly by trial and error. However, ‘Mirror Therapy’&#xD;
has recently been suggested which seems to show promising results for the effective treatment of phantom pain.</description>
    <dc:date>2016-01-01T00:00:00Z</dc:date>
  </item>
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