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Molecular analysis of the iduronate-2-sulfatase gene in Thai patients with Hunter syndrome.
Keeratichamroen S, Cairns JR, Wattanasirichaigoon D, Wasant P, Ngiwsara L, Suwannarat P, Pangkanon S, Kuptanon J, Tanpaiboon P, Rujirawat T, Liammongkolkul S, Svasti J. Keeratichamroen S, et al. Among authors: ngiwsara l. J Inherit Metab Dis. 2008 Dec;31 Suppl 2:S303-11. doi: 10.1007/s10545-008-0876-z. Epub 2008 May 20. J Inherit Metab Dis. 2008. PMID: 18500569
The molecular basis of mucopolysaccharidosis type I in two Thai patients.
Ketudat Cairns JR, Keeratichamroen S, Sukcharoen S, Champattanachai V, Ngiwsara L, Lirdprapamongkol K, Liammongkolkul S, Srisomsap C, Surarit R, Wasant P, Svasti J. Ketudat Cairns JR, et al. Among authors: ngiwsara l. Southeast Asian J Trop Med Public Health. 2005 Sep;36(5):1308-12. Southeast Asian J Trop Med Public Health. 2005. PMID: 16438163
Clinical and molecular characterization of an extended family with Fabry disease.
Wattanasirichaigoon D, Svasti J, Cairns JR, Tangnararatchakit K, Visudtibhan A, Keeratichamroen S, Ngiwsara L, Khowsathit P, Onkoksoong T, Lekskul A, Mongkolsiri D, Jariengprasert C, Thawil C, Ruencharoen S. Wattanasirichaigoon D, et al. Among authors: ngiwsara l. J Med Assoc Thai. 2006 Sep;89(9):1528-35. J Med Assoc Thai. 2006. PMID: 17100396
32 results