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Whole exome sequencing revealed mutations in FBXL4, UNC80, and ADK in Thai patients with severe intellectual disabilities.
Gene. 2019 May 15;696:21-27. doi: 10.1016/j.gene.2019.01.049. Epub 2019 Feb 14.
Gene. 2019.
PMID: 30771478
Mutational and phenotypic expansion of ATP1A3-related disorders: Report of nine cases.
Boonsimma P, Michael Gasser M, Netbaramee W, Wechapinan T, Srichomthong C, Ittiwut C, Wagner M, Krenn M, Zimprich F, Abicht A, Biskup S, Roser T, Borggraefe I, Suphapeetiporn K, Shotelersuk V.
Boonsimma P, et al. Among authors: wechapinan t.
Gene. 2020 Jul 30;749:144709. doi: 10.1016/j.gene.2020.144709. Epub 2020 Apr 25.
Gene. 2020.
PMID: 32339621
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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: wechapinan t.
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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Quality of life in adolescent absence epilepsy at Queen Sirikit National Institute of Child Health.
Suwannachote S, Wechapinan T, Sriudomkajorn S.
Suwannachote S, et al. Among authors: wechapinan t.
J Med Assoc Thai. 2014 Jun;97 Suppl 6:S120-5.
J Med Assoc Thai. 2014.
PMID: 25391183
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Rare epileptic syndrome of ring chromosome 20 with epileptic encephalopathy: a case report.
Wechapinan T, Sri-Udomkajorn S, Suwannachote S.
Wechapinan T, et al.
J Med Assoc Thai. 2014 Jun;97 Suppl 6:S239-42.
J Med Assoc Thai. 2014.
PMID: 25391199
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Heterogenous treatment for anti-NMDAR encephalitis in children leads to different outcomes 6-12 months after diagnosis.
Sakpichaisakul K, Patibat L, Wechapinan T, Sri-Udomkajrorn S, Apiwattanakul M, Suwannachote S.
Sakpichaisakul K, et al. Among authors: wechapinan t.
J Neuroimmunol. 2018 Nov 15;324:119-125. doi: 10.1016/j.jneuroim.2018.09.007. Epub 2018 Sep 19.
J Neuroimmunol. 2018.
PMID: 30269038
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Successful Treatment of Schwartz-Jampel Syndrome with Botulinum Toxin Type A.
Suphatsathienkul P, Sakpichaisakul K, Wechapinan T, Trachoo O, Virawan S, Wanitphakdeedecha R.
Suphatsathienkul P, et al. Among authors: wechapinan t.
Dermatol Ther (Heidelb). 2024 Feb;14(2):545-556. doi: 10.1007/s13555-023-01088-7. Epub 2024 Jan 28.
Dermatol Ther (Heidelb). 2024.
PMID: 38285320
Free PMC article.
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