Literature DB >> 31621611

A novel developmental encephalopathy with epilepsy and hyperkinetic movement disorders associated with a deletion of the sodium channel gene cluster on chromosome 2q24.3.

Mario Mastrangelo1, Davide Mei2, Serena Cesario1, Francesca Fioriello1, Laura Bernardini3, Mario Brinciotti1, Renzo Guerrini2, Vincenzo Leuzzi4.   

Abstract

Entities:  

Keywords:  Developmental; Developmental delay; Dravet syndrome; Epileptic encephalopathies; Hyperkinetic movement disorders

Year:  2019        PMID： 31621611     DOI： 10.1016/j.parkreldis.2019.09.016

Source DB:  PubMed          Journal:  Parkinsonism Relat Disord        ISSN： 1353-8020            Impact factor:   4.891


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  1 in total

1.  Presenting Patterns of Genetically Determined Developmental Encephalopathies With Epilepsy and Movement Disorders: A Single Tertiary Center Retrospective Cohort Study.

Authors:  Mario Mastrangelo; Serena Galosi; Serena Cesario; Alessia Renzi; Lucilla Campea; Vincenzo Leuzzi
Journal:  Front Neurol       Date:  2022-06-20       Impact factor: 4.086
  1 in total

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