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    <title>Hutton, M.</title>
    <link>http://repub.eur.nl/res/aut/5513/</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>Apolipoprotein E genotype does not affect the age of onset of dementia in families with define tau mutations (Article)</title>
      <link>http://repub.eur.nl/res/pub/5886/</link>
      <pubDate>1999-02-05T00:00:00Z</pubDate>
      <description>We have assessed whether apolipoprotein E (ApoE) genotype influences the age of onset of dementia in a series of families with frontal temporal dementia with defined mutations in the tau gene. In contrast to the situation in Alzheimer's disease (AD), we could find no evidence that the age of onset of disease was influenced by the ApoE genotype.</description>
    </item> <item>
      <title>Estimation of the genetic contribution of presenilin-1 and -2 mutations in a population-based study of presenile Alzheimer disease (Article)</title>
      <link>http://repub.eur.nl/res/pub/8752/</link>
      <pubDate>1998-01-01T00:00:00Z</pubDate>
      <description>Two closely related genes, the presenilins ( PS ), located at chromosomes
      14q24.3 and 1q42.1, have been identified for autosomal dominant Alzheimer
      disease (AD) with onset age below 65 years (presenile AD). We performed a
      systematic mutation analysis of all coding and 5'-non-coding exons of PS
      -1 and PS -2 in a population-based epidemiological series of 101 unrelated
      familial and sporadic presenile AD cases. The familial cases included 10
      patients of autosomal dominant AD families sampled for linkage analysis
      studies. In all patients mutations in the amyloid precursor protein gene (
      APP ) had previously been excluded. Four different PS -1 missense
      mutations were identified in six familial cases, two of which where
      autosomal dominant cases. Three mutations resulted in onset ages above 55
      years, with one segregating in an autosomal dominant family with mean
      onset age 64 years (range 50-78 years). One PS -2 mutation was identified
      in a sporadic case with onset age 62 years. Our mutation data provided
      estimates for PS -1 and PS -2 mutation frequencies in presenile AD of 6
      and 1% respectively. When family history was accounted for mutation
      frequencies for PS -1 were 9% in familial cases and 18% in autosomal
      dominant cases. Further, polymorphisms were detected in the promoter and
      the 5'-non-coding region of PS -1 and in intronic and exonic sequences of
      PS -2 that will be useful in genetic association studies.</description>
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