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Epileptogenic Brain Malformations and Mutations in Tubulin Genes: A Case Report and Review of the Literature.
Mencarelli, Annalisa; Prontera, Paolo; Stangoni, Gabriela; Mencaroni, Elisabetta; Principi, Nicola; Esposito, Susanna.
Affiliation
  • Mencarelli A; Pediatric Clinic, Department of Surgical and Biomedical Sciences, Università degli Studi di Perugia, 06123 Perugia, Italy. almiomedico@gmail.com.
  • Prontera P; Medical Genetics Unit, S. Maria della Misericordia Hospital, and University of Perugia, 06123 Perugia, Italy. paolo.prontera@ospedale.perugia.it.
  • Stangoni G; Medical Genetics Unit, S. Maria della Misericordia Hospital, and University of Perugia, 06123 Perugia, Italy. gabriela.stangoni@ospedale.perugia.it.
  • Mencaroni E; Pediatric Clinic, Department of Surgical and Biomedical Sciences, Università degli Studi di Perugia, 06123 Perugia, Italy. elisabetta.mencaroni@ospedale.perugia.it.
  • Principi N; Pediatric Highly Intensive Care Unit, Università degli Studi di Milano, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, 20122 Milano, Italy. nicola.principi@unimi.it.
  • Esposito S; Pediatric Clinic, Department of Surgical and Biomedical Sciences, Università degli Studi di Perugia, 06123 Perugia, Italy. susanna.esposito@unimi.it.
Int J Mol Sci ; 18(11)2017 Oct 29.
Article in En | MEDLINE | ID: mdl-29109381
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tubulin / Mutation, Missense / Epilepsy / Malformations of Cortical Development Type of study: Diagnostic_studies Limits: Child / Female / Humans Language: En Journal: Int J Mol Sci Year: 2017 Document type: Article Affiliation country:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tubulin / Mutation, Missense / Epilepsy / Malformations of Cortical Development Type of study: Diagnostic_studies Limits: Child / Female / Humans Language: En Journal: Int J Mol Sci Year: 2017 Document type: Article Affiliation country: