Compound heterozygosity of a silent beta-thalassemia mutation at the 3′-untranslated region (HBB: c.*132 C>T) and beta-zero thalassemia results in thalassemia intermedia
A Novel GNAS Mutation Causing Isolated Infantile Cushing's Syndrome
Accuracy of the Bilicare™ transcutaneous bilirubinometer as the predischarge screening tool for significant hyperbilirubinemia in healthy term and late preterm neonates
Use and Outcomes of Antiretroviral Monotherapy and Treatment Interruption in Adolescents With Perinatal HIV Infection in Asia
Complementary feeding: Attitudes, knowledge and practices of urban families in northern Thailand.
Hyperuricemia, urine uric excretion, and associated complications in thalassemia patients.
FLT3, a prognostic biomarker for acute myeloid leukemia (AML): Quantitative monitoring with a simple anti-FLT3 interaction and flow cytometric method.
Novel mutations in SPTA1 and SPTB identified by whole exome sequencing in eight Thai families with hereditary pyropoikilocytosis presenting with severe fetal and neonatal anaemia.
Disease- and treatment-related morbidity in adolescents with perinatal HIV infection in Asia.