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Common and rare susceptibility genetic variants predisposing to Brugada syndrome in Thailand.
Makarawate P, Glinge C, Khongphatthanayothin A, Walsh R, Mauleekoonphairoj J, Amnueypol M, Prechawat S, Wongcharoen W, Krittayaphong R, Anannab A, Lichtner P, Meitinger T, Tjong FVY, Lieve KVV, Amin AS, Sahasatas D, Ngarmukos T, Wichadakul D, Payungporn S, Sutjaporn B, Wandee P, Poovorawan Y, Tfelt-Hansen J, Tanck MWT, Tadros R, Wilde AAM, Bezzina CR, Veerakul G, Nademanee K. Makarawate P, et al. Among authors: wandee p. Heart Rhythm. 2020 Dec;17(12):2145-2153. doi: 10.1016/j.hrthm.2020.06.027. Epub 2020 Jun 30. Heart Rhythm. 2020. PMID: 32619740
Clinical Characteristics of SCN5A p.R965C Carriers: A Common Founder Variant Predisposing to Brugada Syndrome in Thailand.
Chimparlee N, Prechawat S, Khongphatthanayothin A, Mauleekoonphairoj J, Lekchuensakul S, Wongcharoen W, Makarawate P, Sahasatas D, Krittayaphong R, Amnueypol M, Anannab A, Ngarmukos T, Vardhanabhuti S, Sutjaporn B, Wandee P, Veerakul G, Bezzina CR, Poovorawan Y, Nademanee K. Chimparlee N, et al. Among authors: wandee p. Circ Genom Precis Med. 2021 Jun;14(3):e003229. doi: 10.1161/CIRCGEN.120.003229. Epub 2021 Jun 7. Circ Genom Precis Med. 2021. PMID: 34092119 Clinical Trial. No abstract available.
Genotype and clinical characteristics of congenital long QT syndrome in Thailand.
Saprungruang A, Khongphatthanayothin A, Mauleekoonphairoj J, Wandee P, Kanjanauthai S, Bhuiyan ZA, Wilde AAM, Poovorawan Y. Saprungruang A, et al. Among authors: wandee p. Indian Pacing Electrophysiol J. 2018 Sep-Oct;18(5):165-171. doi: 10.1016/j.ipej.2018.07.007. Epub 2018 Jul 20. Indian Pacing Electrophysiol J. 2018. PMID: 30036649 Free PMC article.