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Corrigendum: Prader-Willi syndrome: Symptoms and topiramate response in light of genetics.
Louveau, Cécile; Turtulici, Mimi-Caterina; Consoli, Angèle; Poitou, Christine; Coupaye, Muriel; Krebs, Marie-Odile; Chaumette, Boris; Iftimovici, Anton.
Afiliação
  • Louveau C; Centre de Référence pour les Maladies Rares à expression Psychiatrique, GHU Paris Psychiatrie et Neurosciences, Paris, France.
  • Turtulici MC; Centre de Référence pour les Maladies Rares à expression Psychiatrique, GHU Paris Psychiatrie et Neurosciences, Paris, France.
  • Consoli A; Department of Child and Adolescent Psychiatry, Pitié-Salpêtrière Hospital, Paris, France.
  • Poitou C; GRC-15, Dimensional Approach of Child and Adolescent Psychotic Episodes, Faculté de Médecine, Sorbonne Université, Paris, France.
  • Coupaye M; Nutrition Department, Rare Diseases Center of Reference "Prader-Willi Syndrome and Obesity With Eating Disorders" (PRADORT), Assistance Publique-Hôpitaux de Paris, Pitié-Salpêtrière Hospital, INSERM, Nutriomics, Sorbonne Université, Paris, France.
  • Krebs MO; Nutrition Department, Rare Diseases Center of Reference "Prader-Willi Syndrome and Obesity With Eating Disorders" (PRADORT), Assistance Publique-Hôpitaux de Paris, Pitié-Salpêtrière Hospital, INSERM, Nutriomics, Sorbonne Université, Paris, France.
  • Chaumette B; Centre de Référence pour les Maladies Rares à expression Psychiatrique, GHU Paris Psychiatrie et Neurosciences, Paris, France.
  • Iftimovici A; Institute of Psychiatry and Neuroscience of Paris (IPNP), INSERM U1266, Université Paris Cité, Paris, France.
Front Neurosci ; 17: 1189154, 2023.
Article em En | MEDLINE | ID: mdl-37065914

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article