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Perampanel as precision therapy in rare genetic epilepsies.
Epilepsia. 2023 Apr;64(4):866-874. doi: 10.1111/epi.17530. Epub 2023 Feb 20.
Epilepsia. 2023.
PMID: 36734057
Unusual variability of PRRT2 linked phenotypes within a family.
Brueckner F, Kohl B, Puest B, Gassner S, Osseforth J, Lindenau M, Stodieck S, Biskup S, Lohmann E.
Brueckner F, et al. Among authors: puest b.
Eur J Paediatr Neurol. 2014 Jul;18(4):540-2. doi: 10.1016/j.ejpn.2014.03.012. Epub 2014 Apr 8.
Eur J Paediatr Neurol. 2014.
PMID: 24755245
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