Early-onset encephalopathy with paroxysmal movement disorders and epileptic seizures without hemiplegic attacks: About three children with novel ATP1A3 mutations - Archive ouverte HAL Access content directly
Journal Articles Brain and Development Year : 2018

Early-onset encephalopathy with paroxysmal movement disorders and epileptic seizures without hemiplegic attacks: About three children with novel ATP1A3 mutations

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Cyril Mignot
  • Function : Author
  • PersonId : 934439
Nathalie Dorison
  • Function : Author
  • PersonId : 942122
Dorothée Ville
  • Function : Author
  • PersonId : 942119
Anna Kaminska
  • Function : Author
  • PersonId : 942116
Anne-Sophie Dienpendaele
  • Function : Author
Marie-José Penniello
  • Function : Author
Christian Richelme
  • Function : Author
  • PersonId : 889694
Clotilde Rivier
  • Function : Author
Sandra Whalen
Delphine Heron
  • Function : Author
  • PersonId : 906967
Gaetan Lesca
Diane Doummar
  • Function : Author
  • PersonId : 953196
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Dates and versions

hal-01932806 , version 1 (23-11-2018)

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Pauline Marzin, Cyril Mignot, Nathalie Dorison, Louis Claude Dufour, Dorothée Ville, et al.. Early-onset encephalopathy with paroxysmal movement disorders and epileptic seizures without hemiplegic attacks: About three children with novel ATP1A3 mutations. Brain and Development, 2018, 40 (9), pp.768 - 774. ⟨10.1016/j.braindev.2018.05.008⟩. ⟨hal-01932806⟩
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