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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2004 1
2006 1
2007 6
2008 9
2009 5
2010 4
2011 7
2012 8
2013 11
2014 10
2015 12
2016 10
2017 10
2018 15
2019 16
2020 17
2021 4
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125 results
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Page 1
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: suphapeetiporn k. 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: suphapeetiporn k. 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
Whole exome sequencing for diagnosis of hereditary thrombocytopenia.
Mekchay P, Ittiwut C, Ittiwut R, Akkawat B, Le Grand SM, Leela-Adisorn N, Muanpetch S, Khovidhunkit W, Sosothikul D, Shotelersuk V, Suphapeetiporn K, Rojnuckarin P. Mekchay P, et al. Among authors: suphapeetiporn k. Medicine (Baltimore). 2020 Nov 20;99(47):e23275. doi: 10.1097/MD.0000000000023275. Medicine (Baltimore). 2020. PMID: 33217855 Free PMC article.
Expanding phenotypic and mutational spectra of mitochondrial HMG-CoA synthase deficiency.
Rojnueangnit K, Maneechai P, Thaweekul P, Piriyanon P, Khositseth S, Ittiwut C, Chetruengchai W, Kamolvisit W, Theerapanon T, Suphapeetiporn K, Porntaveetus T, Shotelersuk V. Rojnueangnit K, et al. Among authors: suphapeetiporn k. Eur J Med Genet. 2020 Dec;63(12):104086. doi: 10.1016/j.ejmg.2020.104086. Epub 2020 Oct 9. Eur J Med Genet. 2020. PMID: 33045405
Rapid Low-Cost Microarray-Based Genotyping for Genetic Screening in Primary Immunodeficiency.
Suratannon N, van Wijck RTA, Broer L, Xue L, van Meurs JBJ, Barendregt BH, van der Burg M, Dik WA, Chatchatee P, Langerak AW, Swagemakers SMA, Goos JAC, Mathijssen IMJ, Dalm VASH, Suphapeetiporn K, Heezen KC, Drabwell J, Uitterlinden AG, van der Spek PJ, van Hagen PM; South East Asia Primary Immunodeficiencies (SEAPID) Consortium. Suratannon N, et al. Among authors: suphapeetiporn k. Front Immunol. 2020 Apr 15;11:614. doi: 10.3389/fimmu.2020.00614. eCollection 2020. Front Immunol. 2020. PMID: 32373116 Free PMC article.
A Novel GNAS Mutation Causing Isolated Infantile Cushing's Syndrome.
Dejkhamron P, Ittiwut C, TangNgam H, Sunkonkit K, Natesirinilkul R, Suphapeetiporn K, Shotelersuk V. Dejkhamron P, et al. Among authors: suphapeetiporn k. Horm Res Paediatr. 2019;92(3):196-202. doi: 10.1159/000501169. Epub 2019 Jul 30. Horm Res Paediatr. 2019. PMID: 31362300
Founder effect of the TTTCA repeat insertions in SAMD12 causing BAFME1.
Yeetong P, Chunharas C, Pongpanich M, Bennett MF, Srichomthong C, Pasutharnchat N, Suphapeetiporn K, Bahlo M, Shotelersuk V. Yeetong P, et al. Among authors: suphapeetiporn k. Eur J Hum Genet. 2021 Feb;29(2):343-348. doi: 10.1038/s41431-020-00729-1. Epub 2020 Sep 24. Eur J Hum Genet. 2021. PMID: 32973343
Association of IKZF1 SNPs in cold medicine-related Stevens-Johnson syndrome in Thailand.
Chantaren P, Jongkhajornpong P, Ueta M, Puangsricharern V, Lekhanont K, Pisuchpen P, Prabhasawat P, Suphapeetiporn K, Kinoshita S. Chantaren P, et al. Among authors: suphapeetiporn k. Clin Transl Allergy. 2019 Nov 22;9:61. doi: 10.1186/s13601-019-0300-9. eCollection 2019. Clin Transl Allergy. 2019. PMID: 31768251 Free PMC article.
125 results
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