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Childhood opsoclonus-myoclonus syndrome: A case series from Tunisia.
Ben Achour, Nedia; Mrabet, Saloua; Rebai, Ibtihel; Abid, Ines; Benrhouma, Hanene; Klaa, Hedia; Rouissi, Aida; Kraoua, Ichraf; Ben Youssef Turki, Ilhem.
Afiliación
  • Ben Achour N; Research Unit UR12 SP24 and Department of Child and Adolescent Neurology, National Institute Mongi Ben Hmida of Neurology, Tunis, Tunisia; Tunis El Manar University, Faculty of Medicine of Tunis, 1007 Tunis, Tunisia. Electronic address: nediaachour@yahoo.fr.
  • Mrabet S; Research Unit UR12 SP24 and Department of Child and Adolescent Neurology, National Institute Mongi Ben Hmida of Neurology, Tunis, Tunisia.
  • Rebai I; Research Unit UR12 SP24 and Department of Child and Adolescent Neurology, National Institute Mongi Ben Hmida of Neurology, Tunis, Tunisia.
  • Abid I; Research Unit UR12 SP24 and Department of Child and Adolescent Neurology, National Institute Mongi Ben Hmida of Neurology, Tunis, Tunisia.
  • Benrhouma H; Research Unit UR12 SP24 and Department of Child and Adolescent Neurology, National Institute Mongi Ben Hmida of Neurology, Tunis, Tunisia; Tunis El Manar University, Faculty of Medicine of Tunis, 1007 Tunis, Tunisia.
  • Klaa H; Research Unit UR12 SP24 and Department of Child and Adolescent Neurology, National Institute Mongi Ben Hmida of Neurology, Tunis, Tunisia; Tunis El Manar University, Faculty of Medicine of Tunis, 1007 Tunis, Tunisia.
  • Rouissi A; Research Unit UR12 SP24 and Department of Child and Adolescent Neurology, National Institute Mongi Ben Hmida of Neurology, Tunis, Tunisia.
  • Kraoua I; Research Unit UR12 SP24 and Department of Child and Adolescent Neurology, National Institute Mongi Ben Hmida of Neurology, Tunis, Tunisia; Tunis El Manar University, Faculty of Medicine of Tunis, 1007 Tunis, Tunisia.
  • Ben Youssef Turki I; Research Unit UR12 SP24 and Department of Child and Adolescent Neurology, National Institute Mongi Ben Hmida of Neurology, Tunis, Tunisia; Tunis El Manar University, Faculty of Medicine of Tunis, 1007 Tunis, Tunisia.
Brain Dev ; 39(9): 751-755, 2017 Oct.
Article en En | MEDLINE | ID: mdl-28549713
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Opsoclonía-Mioclonía Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male País/Región como asunto: Africa Idioma: En Revista: Brain Dev Año: 2017 Tipo del documento: Article
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Opsoclonía-Mioclonía Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male País/Región como asunto: Africa Idioma: En Revista: Brain Dev Año: 2017 Tipo del documento: Article