Literature DB >> 15096393

Molecular basis of inherited epilepsy.

Alfred L George1.   

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Year:  2004        PMID： 15096393     DOI： 10.1001/archneur.61.4.473

Source DB:  PubMed          Journal:  Arch Neurol        ISSN： 0003-9942


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  3 in total

1.  The GABAA receptor alpha1 subunit epilepsy mutation A322D inhibits transmembrane helix formation and causes proteasomal degradation.

Authors:  Martin J Gallagher; Li Ding; Ankit Maheshwari; Robert L Macdonald
Journal:  Proc Natl Acad Sci U S A       Date:  2007-08-01       Impact factor: 11.205

2.  Prax330 reduces persistent and resurgent sodium channel currents and neuronal hyperexcitability of subiculum neurons in a mouse model of SCN8A epileptic encephalopathy.

Authors:  Eric R Wengert; Anusha U Saga; Payal S Panchal; Bryan S Barker; Manoj K Patel
Journal:  Neuropharmacology       Date:  2019-07-03       Impact factor: 5.250

3.  Whole-Exome Sequencing in Searching for New Variants Associated With the Development of Parkinson's Disease.

Authors:  Marina V Shulskaya; Anelya Kh Alieva; Ivan N Vlasov; Vladimir V Zyrin; Ekaterina Yu Fedotova; Natalia Yu Abramycheva; Tatiana S Usenko; Andrei F Yakimovsky; Anton K Emelyanov; Sofya N Pchelina; Sergei N Illarioshkin; Petr A Slominsky; Maria I Shadrina
Journal:  Front Aging Neurosci       Date:  2018-05-15       Impact factor: 5.750
  3 in total

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