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      <title> L&#39;amyotrophie spinale 1 gpe 2 fenêtres by Samuel Monvoisin</title>
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      <pubDate>2016-11-22 10:23:41 UTC</pubDate>
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         <title>La prise en charge de la maladie</title>
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         <title>Le diagnostic prénatal</title>
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         <description><![CDATA[<div>Pourquoi? Comment?</div>]]></description>
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         <title>Le risque de transmission de la maladie (pour un couple ayant déjà un enfant atteint)</title>
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         <title>L&#39;évolution de la maladie</title>
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         <title>Le phénotype macroscopique</title>
         <author>samonvoisin</author>
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         <title>Le phénotype organique</title>
         <author>samonvoisin</author>
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         <title>Le phénotype cellulaire</title>
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         <title>Le phénotype moléculaire</title>
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         <title>Le génotype</title>
         <author>samonvoisin</author>
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         <title>L&#39;amyotrophie spinale de type 1</title>
         <author>samonvoisin</author>
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         <description><![CDATA[<div>Les amyotrophies spinales sont des affections dues à la dégénérescence des cellules nerveuses qui stimulent et commandent <br>ces muscles (les motoneurones). Elles n’affectent en aucun cas les fonctions intellectuelles.<br><br><strong>Problème: Quelle est l'origine de cette maladie et comment les malades sont ils pris en charge?</strong></div>]]></description>
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