Deep brain stimulation for status dystonicus in a toddler with SCN2A-related disorder
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s00381-023-06136-3.pdf
Reference8 articles.
1. Nakamura K, Kato M, Osaka H, Yamashita S, Nakagawa E, Haginoya K et al (2013) Clinical spectrum of SCN2A mutations expanding to Ohtahara syndrome. Neurology 81:992–998. https://doi.org/10.1212/WNL.0B013E3182A43E57
2. Beal JC, Cherian K, Moshe SL (2012) Early-onset epileptic encephalopathies: Ohtahara syndrome and early myoclonic encephalopathy. Pediatr Neurol 47:317–323. https://doi.org/10.1016/J.PEDIATRNEUROL.2012.06.002
3. Pavone P, Spalice A, Polizzi A, Parisi P, Ruggieri M (2012) Ohtahara syndrome with emphasis on recent genetic discovery. Brain Dev 34:459–468. https://doi.org/10.1016/J.BRAINDEV.2011.09.004
4. Yamatogi Y, Ohtahara S (2002) Early-infantile epileptic encephalopathy with suppression-bursts, Ohtahara syndrome; its overview referring to our 16 cases. Brain Dev 24:13–23
5. Yan H, Siegel L, Breitbart S, Gorodetsky C, Gonorazky HD, Yau I et al (2021) The child & youth CompreHensIve Longitudinal Database for Deep Brain Stimulation (CHILD-DBS). Childs Nerv Syst 37:607–615. https://doi.org/10.1007/S00381-020-04880-4
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