Literature DB >> 21395569

Proposed genetic classification of the "benign" familial neonatal and infantile epilepsies.

John C Mulley1, Sarah E Heron, Leanne M Dibbens.   

Abstract

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Year:  2011        PMID： 21395569     DOI： 10.1111/j.1528-1167.2010.02953.x

Source DB:  PubMed          Journal:  Epilepsia        ISSN： 0013-9580            Impact factor:   5.864


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  4 in total

1.  PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome.

Authors:  Sarah E Heron; Bronwyn E Grinton; Sara Kivity; Zaid Afawi; Sameer M Zuberi; James N Hughes; Clair Pridmore; Bree L Hodgson; Xenia Iona; Lynette G Sadleir; James Pelekanos; Eric Herlenius; Hadassa Goldberg-Stern; Haim Bassan; Eric Haan; Amos D Korczyn; Alison E Gardner; Mark A Corbett; Jozef Gécz; Paul Q Thomas; John C Mulley; Samuel F Berkovic; Ingrid E Scheffer; Leanne M Dibbens
Journal:  Am J Hum Genet       Date:  2012-01-13       Impact factor: 11.025

2.  Genetic variations and associated pathophysiology in the management of epilepsy.

Authors:  John C Mulley; Leanne M Dibbens
Journal:  Appl Clin Genet       Date:  2011-08-08

Review 3.  Epilepsy syndromes during the first year of life and the usefulness of an epilepsy gene panel.

Authors:  Eun Hye Lee
Journal:  Korean J Pediatr       Date:  2018-04-23

Review 4.  Epilepsy Syndromes in the First Year of Life and Usefulness of Genetic Testing for Precision Therapy.

Authors:  Allan Bayat; Michael Bayat; Guido Rubboli; Rikke S Møller
Journal:  Genes (Basel)       Date:  2021-07-08       Impact factor: 4.096
  4 in total

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