Literature DB >> 24090771

Clarifying the role of the 22q11.2 microdeletion in juvenile myoclonic epilepsy.

Ingo Helbig1, Corinna Hartmann, Heather C Mefford.   

Abstract

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Year:  2013        PMID: 24090771     DOI: 10.1016/j.yebeh.2013.08.032

Source DB:  PubMed          Journal:  Epilepsy Behav        ISSN: 1525-5050            Impact factor:   2.937


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  2 in total

1.  Generalized Epilepsy and Myoclonic Seizures in 22q11.2 Deletion Syndrome.

Authors:  Vincent Strehlow; Marielle E M Swinkels; Rhys H Thomas; Nora Rapps; Steffen Syrbe; Thomas Dorn; Johannes R Lemke
Journal:  Mol Syndromol       Date:  2016-08-24

2.  Abnormal hippocampal structure and function in juvenile myoclonic epilepsy and unaffected siblings.

Authors:  Lorenzo Caciagli; Britta Wandschneider; Fenglai Xiao; Christian Vollmar; Maria Centeno; Sjoerd B Vos; Karin Trimmel; Meneka K Sidhu; Pamela J Thompson; Gavin P Winston; John S Duncan; Matthias J Koepp
Journal:  Brain       Date:  2019-09-01       Impact factor: 13.501

  2 in total

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