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    <title>Cardoso, J.</title>
    <link>http://repub.eur.nl/res/aut/15417/</link>
    <description>List of Publications</description>
    <language>en</language>
    <image>
      <url>http://repub.eur.nl/static-eur/img/logo.png</url>
      <title>RePub, Erasmus University Rotterdam</title>
      <link>http://repub.eur.nl</link>
    </image>
    <item>
      <title>Aquatic exercise &amp; balneotherapy in musculoskeletal conditions (Article)</title>
      <link>http://repub.eur.nl/res/pub/39351/</link>
      <pubDate>2012-06-01T00:00:00Z</pubDate>
      <description>This is a best-evidence synthesis providing an evidence-based summary on the effectiveness of aquatic exercises and balneotherapy in the treatment of musculoskeletal conditions. The most prevalent musculoskeletal conditions addressed in this review include: low back pain, osteoarthritis, fibromyalgia and rheumatoid arthritis. Over 30 years of research demonstrates that exercises in general, and specifically aquatic exercises, are beneficial for reducing pain and disability in many musculoskeletal conditions demonstrating small to moderate effect sizes ranging between 0.19 and 0.32. Balneotherapy might be beneficial, but the evidence is yet insufficient to make a definitive statement about its use. High-quality trials are needed on balneotherapy and aquatic exercises research especially in specific patient categories that might benefit most. </description>
    </item> <item>
      <title>Genomic profiling by DNA amplification of laser capture microdissected tissues and array CGH. (Article)</title>
      <link>http://repub.eur.nl/res/pub/13533/</link>
      <pubDate>2004-01-01T00:00:00Z</pubDate>
      <description>Comparative genomic hybridization by means of BAC microarrays (array CGH)
      allows high-resolution profiling of copy-number aberrations in tumor DNA.
      However, specific genetic lesions associated with small but clinically
      relevant tumor areas may pass undetected due to intra-tumor heterogeneity
      and/or the presence of contaminating normal cells. Here, we show that the
      combination of laser capture microdissection, phi29 DNA
      polymerase-mediated isothermal genomic DNA amplification, and array CGH
      allows genomic profiling of very limited numbers of cells. Moreover, by
      means of simple statistical models, we were able to bypass the exclusion
      of amplification distortions and variability prone areas, and to detect
      tumor-specific chromosomal gains and losses. We applied this new combined
      experimental and analytical approach to the genomic profiling of
      colorectal adenomatous polyps and demonstrated our ability to accurately
      detect single copy gains and losses affecting either whole chromosomes or
      small genomic regions from as little as 2 ng of DNA or 1000 microdissected
      cells.</description>
    </item>
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