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Mutational and phenotypic expansion of ATP1A3-related disorders: Report of nine cases.
Gene. 2020 Jul 30;749:144709. doi: 10.1016/j.gene.2020.144709. Epub 2020 Apr 25.
Gene. 2020.
PMID: 32339621
ATP1A3-related epilepsy: Report of seven cases and literature-based analysis of treatment response.
Gasser M, Boonsimma P, Netbaramee W, Wechapinan T, Srichomthomg C, Ittiwut C, Krenn M, Zimprich F, Milenkovic I, Abicht A, Biskup S, Roser T, Shotelersuk V, Tacke M, Kuersten M, Wagner M, Borggraefe I, Suphapeetiporn K, von Stülpnagel C.
Gasser M, et al. Among authors: netbaramee w.
J Clin Neurosci. 2020 Feb;72:31-38. doi: 10.1016/j.jocn.2020.01.041. Epub 2020 Jan 17.
J Clin Neurosci. 2020.
PMID: 31959558
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Phenytoin toxicity in two-month-old Thai infant with CYP2C9 gene polymorphism--A case report.
Veeravigrom M, Jaroonvanichkul V, Netbaramee W, Phaisarn P, Uyathanarat T.
Veeravigrom M, et al. Among authors: netbaramee w.
Brain Dev. 2016 Jan;38(1):136-8. doi: 10.1016/j.braindev.2015.05.001. Epub 2015 May 18.
Brain Dev. 2016.
PMID: 25998968
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Clinical manifestations, treatment outcomes, and prognostic factors of pediatric anti-NMDAR encephalitis in tertiary care hospitals: A multicenter retrospective/prospective cohort study.
Pruetarat N, Netbaramee W, Pattharathitikul S, Veeravigrom M.
Pruetarat N, et al. Among authors: netbaramee w.
Brain Dev. 2019 May;41(5):436-442. doi: 10.1016/j.braindev.2018.12.009. Epub 2019 Jan 11.
Brain Dev. 2019.
PMID: 30639077
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