Literature DB >> 10961647

Calcium channel defects in models of inherited generalized epilepsy.

D L Burgess1, J L Noebels.   

Abstract

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Year:  2000        PMID： 10961647     DOI： 10.1111/j.1528-1157.2000.tb00305.x

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


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  4 in total

1.  Mapping genetic modifiers of survival in a mouse model of Dravet syndrome.

Authors:  A R Miller; N A Hawkins; C E McCollom; J A Kearney
Journal:  Genes Brain Behav       Date:  2013-11-14       Impact factor: 3.449

Review 2.  Identification of epilepsy genes in human and mouse.

Authors:  M H Meisler; J Kearney; R Ottman; A Escayg
Journal:  Annu Rev Genet       Date:  2001       Impact factor: 16.830

Review 3.  WONOEP appraisal: new genetic approaches to study epilepsy.

Authors:  Elsa Rossignol; Katja Kobow; Michele Simonato; Jeffrey A Loeb; Thierry Grisar; Krista L Gilby; Jonathan Vinet; Shilpa D Kadam; Albert J Becker
Journal:  Epilepsia       Date:  2014-06-25       Impact factor: 5.864

Review 4.  The role of T-type calcium channel genes in absence seizures.

Authors:  Yucai Chen; William Davis Parker; Keling Wang
Journal:  Front Neurol       Date:  2014-05-09       Impact factor: 4.003
  4 in total

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