Laurence Lion-Francois

Summary

Affiliation: Hospices Civils de Lyon
Country: France

Publications

  1. ncbi request reprint [Convulsions in infants and children]
    Laurence Lion-Francois
    Service de Neurologie Pediatrique, Hopital Debrousse, Lyon
    Rev Prat 56:201-5. 2006
  2. ncbi request reprint High frequency of creatine deficiency syndromes in patients with unexplained mental retardation
    L Lion-Francois
    Service de Neurologie Pediatrique, Hopital Debrousse, Hospices Civils de Lyon, France
    Neurology 67:1713-4. 2006
  3. doi request reprint Severe neonatal episodic laryngospasm due to de novo SCN4A mutations: a new treatable disorder
    L Lion-Francois
    Hopital Femme Mere Enfant, 59, boulevard Pinel, 69 677 Bron Cedex, France
    Neurology 75:641-5. 2010
  4. pmc Screening for primary creatine deficiencies in French patients with unexplained neurological symptoms
    David Cheillan
    Hospices Civils de Lyon, Service Maladies Héréditaires du Métabolisme et Dépistage Néonatal, Groupement Hospitalier, Bron, France
    Orphanet J Rare Dis 7:96. 2012

Detail Information

Publications4

  1. ncbi request reprint [Convulsions in infants and children]
    Laurence Lion-Francois
    Service de Neurologie Pediatrique, Hopital Debrousse, Lyon
    Rev Prat 56:201-5. 2006
  2. ncbi request reprint High frequency of creatine deficiency syndromes in patients with unexplained mental retardation
    L Lion-Francois
    Service de Neurologie Pediatrique, Hopital Debrousse, Hospices Civils de Lyon, France
    Neurology 67:1713-4. 2006
  3. doi request reprint Severe neonatal episodic laryngospasm due to de novo SCN4A mutations: a new treatable disorder
    L Lion-Francois
    Hopital Femme Mere Enfant, 59, boulevard Pinel, 69 677 Bron Cedex, France
    Neurology 75:641-5. 2010
    ..Myotonia is unusual in infants, and not well-known...
  4. pmc Screening for primary creatine deficiencies in French patients with unexplained neurological symptoms
    David Cheillan
    Hospices Civils de Lyon, Service Maladies Héréditaires du Métabolisme et Dépistage Néonatal, Groupement Hospitalier, Bron, France
    Orphanet J Rare Dis 7:96. 2012
    ....