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  <channel>
    <title>Waasdorp, C.M.</title>
    <link>http://repub.eur.nl/res/aut/9654/</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>A prospective 10 year follow up study of patients with neurofibromatosis type 1 (Article)</title>
      <link>http://repub.eur.nl/res/pub/8858/</link>
      <pubDate>1998-01-01T00:00:00Z</pubDate>
      <description>OBJECTIVE: To establish the prevalence and incidence of symptoms and
          complications in children with neurofibromatosis type 1 (NF1) and to
          assess possible risk factors for the development of complications. DESIGN:
          A 10 year prospective multidisciplinary follow up study. PATIENTS: One
          hundred and fifty children diagnosed with NF1 according to criteria set by
          the National Institutes of Health. RESULTS: In 62 of 150 children (41.3%)
          complications were present, including 42 (28.0%) children with one
          complication, 18 (12.0%) with two complications, and two (1.3%) with three
          complications (mean (SD) duration of follow up 4.9 (3.8) years). Ninety
          five of the 150 children presented without complications (follow up, 340.8
          person-years). The incidence of complications was 2.4/100 person-years in
          this group. An association was found between behavioural problems and the
          presence of complications. CONCLUSION: This is the largest single centre
          case series of NF1 affected children followed until 18 years of age.
          Children with NF1, including those initially presenting without
          complications, should have regular clinical examinations.</description>
    </item>
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