L-serine treatment in a patient with refractory epilepsy due to a GRIN2A missense mutation
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s13760-024-02616-8.pdf
Reference5 articles.
1. Soto D, Olivella M, Grau C, Armstrong J, Alcon C, Gasull X et al (2019) L-Serine dietary supplementation is associated with clinical improvement of loss-of-function GRIN2B-related pediatric encephalopathy. Sci Signal 12. https://doi.org/10.1126/scisignal.aaw0936
2. Julia-Palacios N, Olivella M, Sigatullina Bondarenko M, Ibanez-Mico S, Munoz-Cabello B, Alonso-Luengo O et al (2024) L-serine treatment in patients with GRIN-related encephalopathy: a phase 2A, non-randomized study. Brain. https://doi.org/10.1093/brain/awae041
3. Krey I, von Spiczak S, Johannesen KM, Hikel C, Kurlemann G, Muhle H et al (2022) L-Serine treatment is Associated with improvements in Behavior, EEG, and seizure frequency in individuals with GRIN-cRelated disorders due to null variants. Neurotherapeutics 19:334–341. https://doi.org/10.1007/s13311-021-01173-9
4. den Hollander B, Rothuizen-Lindenschot M, Geertjens L, Vaz FM, Brands MM, Le HL et al (2023) Effectiveness of L-serine supplementation in children with a GRIN2B loss-of-function mutation: Rationale and protocol for single patient (n-of-1) multiple cross-over trials. Contemp Clin Trials Commun 36:101233. https://doi.org/10.1016/j.conctc.2023.101233
5. Swanger SA, Chen W, Wells G, Burger PB, Tankovic A, Bhattacharya S et al (2016) Mechanistic insight into NMDA receptor dysregulation by rare variants in the GluN2A and GluN2B agonist binding domains. Am J Hum Genet 99:1261–1280. https://doi.org/10.1016/j.ajhg.2016.10.002
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