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CACNA1A-associated epilepsy: Electroclinical findings and treatment response on seizures in 18 patients.
Le Roux, Marie; Barth, Magalie; Gueden, Sophie; Desbordes de Cepoy, Patrick; Aeby, Alec; Vilain, Catheline; Hirsch, Edouard; de Saint Martin, Anne; Portes, Vincent des; Lesca, Gaëtan; Riquet, Audrey; Chaton, Laurence; Villeneuve, Nathalie; Villard, Laurent; Cances, Claude; Valton, Luc; Renaldo, Florence; Vermersch, Anne-Isabelle; Altuzarra, Cecilia; Nguyen-Morel, Marie-Ange; Van Gils, Julien; Angelini, Chloé; Biraben, Arnaud; Arnaud, Lionel; Riant, Florence; Van Bogaert, Patrick.
Afiliação
  • Le Roux M; Department of Pediatric Neurology and Neurosurgery, CHU Angers, France. Electronic address: Marie.Le-Roux@chu-angers.fr.
  • Barth M; Department of Medical Genetics, CHU Angers, France.
  • Gueden S; Department of Pediatric Neurology and Neurosurgery, CHU Angers, France.
  • Desbordes de Cepoy P; Department of Pediatric Radiology, CHU Angers, France.
  • Aeby A; Department of Pediatric Neurology, HUDERF, Bruxelles, Belgium.
  • Vilain C; Department of Medical Genetics, Erasme Hospital, Bruxelles, Belgium.
  • Hirsch E; Department of Neurology, CHU Strasbourg, France.
  • de Saint Martin A; Department of Pediatrics, CHU Strasbourg, France.
  • Portes VD; Department of Pediatric Neurology, Hospices civils de Lyon, Bron, France.
  • Lesca G; Department of Genetics, Hospices civils de Lyon, Bron, France.
  • Riquet A; Department of Pediatric Neurology, CHRU Lille, France.
  • Chaton L; Department of Neurophysiology, CHRU Lille, France.
  • Villeneuve N; Department of Pediatric Neurology, Hôpital de La Timone, AP-HM, Marseille, France.
  • Villard L; Department of Medical Genetics, Hôpital de La Timone, AP-HM, Marseille, France; Aix Marseille Univ, Inserm, Marseille Medical Genetics, U1251, Marseille, France.
  • Cances C; Department of Pediatric Neurology, CHU Purpan, Toulouse, France.
  • Valton L; Explorations Neurophysiologiques, CHU Purpan, Toulouse, France; Centre de Recherche Cerveau et Cognition (CerCo), University of Toulouse, Toulouse F, 31300, France.
  • Renaldo F; Department of Pediatric Neurology, Hôpital Trousseau, Assistance publique-Hôpitaux de Paris, France.
  • Vermersch AI; Department of Neurophysiology, Hôpital Trousseau, Assistance publique-Hôpitaux de Paris, France.
  • Altuzarra C; Department of Pediatrics, CHU Besançon, France.
  • Nguyen-Morel MA; Department of Pediatric Neurology, CHU Grenoble Alpes, France.
  • Van Gils J; Department of Medical Genetics, CHU Bordeaux Pellegrin, Bordeaux, France.
  • Angelini C; Department of Medical Genetics, CHU Bordeaux Pellegrin, Bordeaux, France.
  • Biraben A; Department of Neurology, CHU Rennes Pontchaillou, Rennes, France.
  • Arnaud L; Department of Genetics, Hôpital de la Pitie Salpetrière, Assistance publique-Hôpitaux de Paris, France.
  • Riant F; Department of Genetics, Groupe hospitalier Saint Louis-Lariboisière, Assistance publique-Hôpitaux de Paris, France.
  • Van Bogaert P; Department of Pediatric Neurology and Neurosurgery, CHU Angers, France; Laboratoire Angevin de Recherche en Ingénierie des Systèmes (LARIS), Université d'Angers, France.
Eur J Paediatr Neurol ; 33: 75-85, 2021 Jul.
Article em En | MEDLINE | ID: mdl-34102571

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Convulsões / Canais de Cálcio / Epilepsia Tipo de estudo: Diagnostic_studies / Etiology_studies / Risk_factors_studies Limite: Child, preschool / Female / Humans / Male Idioma: En Revista: Eur J Paediatr Neurol Assunto da revista: NEUROLOGIA / PEDIATRIA Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Convulsões / Canais de Cálcio / Epilepsia Tipo de estudo: Diagnostic_studies / Etiology_studies / Risk_factors_studies Limite: Child, preschool / Female / Humans / Male Idioma: En Revista: Eur J Paediatr Neurol Assunto da revista: NEUROLOGIA / PEDIATRIA Ano de publicação: 2021 Tipo de documento: Article