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Polymicrogyria with Dysmorphic Neurons in a Patient with SNCA2 Mutation.
Gelot, Antoinette-Bernabe; Courtin, Thomas; Sileo, Chiara; Keren, Boris; Soreze-Smagghue, Yohan; Whalen, Sandra; Represa, Alfonso.
Affiliation
  • Gelot AB; INMED, INSERM, Aix-Marseille University, Marseille, France.
  • Courtin T; Neuropathology, Hôpital Trousseau, Assistance Publique-Hôpitaux Parisiens (AP-HP), Sorbonne Université, Paris, France.
  • Sileo C; Genetic Department, Centre de Référence des Déficiences Intellectuelles de Causes Rares, GRC UPMC, "Déficiences Intellectuelles et Autisme", Hôpital de la Pitié-Salpêtrière, Paris, France.
  • Keren B; Department of Pediatric Imaging, Hôpital Trousseau, Assistance Publique-Hôpitaux Parisiens (AP-HP), Sorbonne Université, Paris, France.
  • Soreze-Smagghue Y; Genetic Department, Centre de Référence des Déficiences Intellectuelles de Causes Rares, GRC UPMC, "Déficiences Intellectuelles et Autisme", Hôpital de la Pitié-Salpêtrière, Paris, France.
  • Whalen S; Paediatric and Neonatal Reanimation, Hôpital Trousseau, Assistance Publique-Hôpitaux Parisiens (AP-HP), Sorbonne Université, Paris, France.
  • Represa A; Genetic Department, Hôpital Trousseau, Assistance Publique-Hôpitaux Parisiens (AP-HP), Sorbonne Université, Paris, France.
J Neuropathol Exp Neurol ; 81(9): 758-761, 2022 08 16.
Article in En | MEDLINE | ID: mdl-35788683
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Malformations of Cortical Development / Polymicrogyria Limits: Humans Language: En Journal: J Neuropathol Exp Neurol Year: 2022 Document type: Article Affiliation country: Country of publication:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Malformations of Cortical Development / Polymicrogyria Limits: Humans Language: En Journal: J Neuropathol Exp Neurol Year: 2022 Document type: Article Affiliation country: Country of publication: