<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Dill P</dc:creator>
  <dc:creator>Wagner M</dc:creator>
  <dc:creator>Somerville A</dc:creator>
  <dc:creator>Thöny B</dc:creator>
  <dc:creator>Blau N</dc:creator>
  <dc:creator>Weber P</dc:creator>
  <dc:date>2012</dc:date>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://sonar.ch/global/documents/143311</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1212/WNL.0b013e3182452849</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/22291068</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:source>Neurology. - 2012</dc:source>
  <dc:subject xmlns:ns0="xml" ns0:lang="en">5-Hydroxytryptophan</dc:subject>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Alcohol Oxidoreductases</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Behavior</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Benserazide</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Consanguinity</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Developmental Disabilities</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Dopamine Agents</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">Drug Combinations</dc:subject>
  <dc:subject xmlns:ns8="xml" ns8:lang="en">Eye Movements</dc:subject>
  <dc:subject xmlns:ns9="xml" ns9:lang="en">Female</dc:subject>
  <dc:subject xmlns:ns10="xml" ns10:lang="en">Humans</dc:subject>
  <dc:subject xmlns:ns11="xml" ns11:lang="en">Infant</dc:subject>
  <dc:subject xmlns:ns12="xml" ns12:lang="en">Levodopa</dc:subject>
  <dc:subject xmlns:ns13="xml" ns13:lang="en">Movement Disorders</dc:subject>
  <dc:subject xmlns:ns14="xml" ns14:lang="en">Muscle Hypotonia</dc:subject>
  <dc:subject xmlns:ns15="xml" ns15:lang="en">Nervous System Diseases</dc:subject>
  <dc:subject xmlns:ns16="xml" ns16:lang="en">Neurotransmitter Agents</dc:subject>
  <dc:subject xmlns:ns17="xml" ns17:lang="en">Phenylketonurias</dc:subject>
  <dc:subject xmlns:ns18="xml" ns18:lang="en">Treatment Outcome</dc:subject>
  <dc:title xmlns:ns19="xml" ns19:lang="en">Child neurology: paroxysmal stiffening, upward gaze, and hypotonia: hallmarks of sepiapterin reductase deficiency.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>