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Role of a homozygous A(TA)?TAA promoter polymorphism and an exon 1 heterozygous frameshift mutation UGT1A1 in Crigler-Najjar syndrome type II in a Thai neonate. Nilyanimit P, Krasaelap A, Foonoi M, Chongsrisawat V, Poovorawan Y. Genet Mol Res. 2013;12(3):3391-7.
Association between UGT 1A1 Gly71Arg (G71R) polymorphism and neonatal hyperbilirubinemia. Prachukthum S, Gamnarai P, Kangsadalampai S. J Med Assoc Thai. 2012 Jan;95 Suppl 1:S13-7.
Incidence and risk factors of parenteral nutrition-associated liver disease in newborn infants. Koseesirikul P, Chotinaruemol S, Ukarapol N. Pediatr Int. 2012;54(3):434-6.
Early Treatment With Ursodeoxycholic Acid For Total Parenteral Nutrition Associated Cholestasis. In newborn. Intab N, Thantithaveewat T. Thai J Pediatr 2011;50:102-11
Diagnostic evaluation of infantile cholestasis. Wongsawasdi L, Ukarapol N, Visrutaratna P, Singhavejsakul J, Kattipattanapong V. J Med Assoc Thai. 2008 Mar;91(3):345-9.
Neonatal Cholestasis in Thai infants. Aanpreung P, Laohapansang M, Ruangtrakool R, Kimhan J. J Med Assoc Thai 2005; 88(Suppl 8):S9-15.
Relationship between vasoactive intestinal peptide and intrapulmonary vascular dilatation in children with various liver diseases. Chongsrisawat V, Ampai S, Chotivitayatarakorn P, Sirisopikul T, Poovorawan Y. ActaPaediatr. 2003;92(12):1411-4.
Neonatal Cholestasis : Biliary Artesia, the Possible Solution. Kosuwon P, Aremitra S, Sumit S, Tantiyasawasdikul V, Mekanantawat M. Srinagarind Med J 2001; 16(4); 257-63.