Perampanel as precision therapy in rare genetic epilepsies (vol 64, pg 866, 2023)

A. Nissenkorn,G. Kluger,S. Schubert-Bast,A. Bayat, M. Bobylova,P. Bonanni,B. Ceulemans,A. Coppola,C. Di Bonaventura,M. Feucht, A. Fuchs,G. Groppel,G. Heimer, B. Herdt, S. Kulikova,K. Mukhin, S. Nicassio,A. Orsini, M. Panagiotou,M. Pringsheim, B. Fuest,O. Pylaeva,G. Ramantani, M. Tsekoura,P. Ricciardelli, T. Lerman Sagie, B. Stark,P. Striano,A. van Baalen,M. De Wachter,E. Cerulli Irelli,C. von Stulpnagel,A. Russo

EPILEPSIA（2024）

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摘要

Perampanel demonstrated high safety and efficacy in patients with rare genetic epilepsies, especially in SCN1A, GNAO1, PIGA, PCDH19, SYNGAP1, CDKL5, NEU1 and POLG, suggesting a targeted effect related to glutamate transmission.

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Perampanel,genetic epilepsies,precision therapy

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