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Review

Precision medicine in genetic epilepsies: break of dawn?

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Pages 381-392 | Received 29 Jul 2016, Accepted 11 Oct 2016, Published online: 10 Nov 2016

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Qiang Li, M. Brandon Westover, Rui Zhang & Catherine J. Chu. (2021) Computational Evidence for a Competitive Thalamocortical Model of Spikes and Spindle Activity in Rolandic Epilepsy. Frontiers in Computational Neuroscience 15.
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Laurent M. Willems, Adam Strzelczyk & Felix Rosenow. (2021) Everolimus als krankheitsspezifische Therapieoption bei mit tuberöser Sklerose assoziierter, therapierefraktärer Epilepsie – ein systematischer ÜberblickEverolimus as disease-specific treatment option in tuberous sclerosis complex-associated drug refractory epilepsy—a systematic review. Zeitschrift für Epileptologie 34:2, pages 168-174.
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Anna Portale, Mattia Comella, Giulia Salomone, Alessandra Di Nora, Lidia Marino, Roberta Leonardi, Andrea D. Praticò & Raffaele Falsaperla. (2021) The Spectrum of KCNQ2- and KCNQ3-Related Epilepsy. Journal of Pediatric Neurology.
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D. Chiarello, F. Duranti, A. Lividini, L. Maltoni, C. Spadoni, S. Taormina, D.M. Cordelli, E. Franzoni & A. Parmeggiani. (2020) Clinical characterization of status epilepticus in childhood: a retrospective study in 124 patients. Seizure 78, pages 127-133.
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Pasquale Striano & Berge A. Minassian. (2020) From Genetic Testing to Precision Medicine in Epilepsy. Neurotherapeutics 17:2, pages 609-615.
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Maurits W. C. B. Sanders, Cynthia M. C. Lemmens, Floor E. Jansen, Eva H. Brilstra, Bobby P. C. Koeleman & Kees P. J. Braun. (2019) Implications of genetic diagnostics in epilepsy surgery candidates: A single‐center cohort study. Epilepsia Open 4:4, pages 609-617.
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Piero Perucca & Emilio Perucca. (2019) Identifying mutations in epilepsy genes: Impact on treatment selection. Epilepsy Research 152, pages 18-30.
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Ahsan N. V. Moosa. (2019) Antiepileptic Drug Treatment of Epilepsy in Children. CONTINUUM: Lifelong Learning in Neurology 25:2, pages 381-407.
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Ana Vilan, José Mendes Ribeiro, Pasquale Striano, Sarah Weckhuysen, Lauren C. Weeke, Eva Brilstra, Linda S. de Vries & Maria Roberta Cilio. (2017) A Distinctive Ictal Amplitude-Integrated Electroencephalography Pattern in Newborns with Neonatal Epilepsy Associated with <b><i>KCNQ2</i></b> Mutations. Neonatology 112:4, pages 387-393.
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