Heterogenous treatment for anti-NMDAR encephalitis in children leads to different outcomes 6–12 months after diagnosis
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Published in Journal of neuroimmunology (15.11.2018)
Published in Journal of neuroimmunology (15.11.2018)
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Whole exome sequencing revealed mutations in FBXL4, UNC80, and ADK in Thai patients with severe intellectual disabilities
Kuptanon, Chulaluck, Srichomthong, Chalurmpon, Ittiwut, Chupong, Wechapinan, Thanin, Sri-Udomkajorn, Somjit, Iamopas, Orawan, Phokaew, Chureerat, Suphapeetiporn, Kanya, Shotelersuk, Vorasuk
Published in Gene (15.05.2019)
Published in Gene (15.05.2019)
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Mutational and phenotypic expansion of ATP1A3-related disorders: Report of nine cases
Boonsimma, Ponghatai, Michael Gasser, Marius, Netbaramee, Wiracha, Wechapinan, Thanin, Srichomthong, Chalurmpon, Ittiwut, Chupong, Wagner, Matias, Krenn, Martin, Zimprich, Fritz, Abicht, Angela, Biskup, Saskia, Roser, Timo, Borggraefe, Ingo, Suphapeetiporn, Kanya, Shotelersuk, Vorasuk
Published in Gene (30.07.2020)
Published in Gene (30.07.2020)
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ATP1A3-related epilepsy: Report of seven cases and literature-based analysis of treatment response
Gasser, Marius, Boonsimma, Ponghatai, Netbaramee, Wiracha, Wechapinan, Thanin, Srichomthomg, Chalurmpon, Ittiwut, Chupong, Krenn, Martin, Zimprich, Fritz, Milenkovic, Ivan, Abicht, Angela, Biskup, Saskia, Roser, Timo, Shotelersuk, Vorasuk, Tacke, Moritz, Kuersten, Marianne, Wagner, Matias, Borggraefe, Ingo, Suphapeetiporn, Kanya, von Stülpnagel, Celina
Published in Journal of clinical neuroscience (01.02.2020)
Published in Journal of clinical neuroscience (01.02.2020)
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