Variant nonketotic hyperglycinemia caused by a novel pathogenic mutation in the glrx5 gene
พ.ศ. 2563
Clinical, biochemical and molecular profile of variant galactosemia in children detected by national newborn screening: A pilot study
พ.ศ. 2560
Screening of Glucose-6-Phosphate Dehydrogenase Deficiency in Neonatal Hyperbilirubinaemia at 300-Bedded Pyin Oo Lwin General Hospital
พ.ศ. 2562
Diabetic ketoacidosis at diagnosis of type 1 diabetes mellitus in Malaysian children and adolescents
พ.ศ. 2559
RELATIONSHIP BETWEEN GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY AND UGT1A1 GENOTYPES IN NEONATES WITH HYPERBILIRUBINEMIA
มหาวิทยาลัยขอนแก่น พ.ศ. 2560
Clinical Profiles and Outcomes of the Most Common Inherited Metabolic Diseases in the Philippines: A Review of the National Institutes of Health – Institute of Human Genetics Metabolic Registry
พ.ศ. 2563
Diabetic ketoacidosis in children: an 11-year retrospective in Surabaya, Indonesia
Universitas Airlangga พ.ศ. 2558
Lack of meaningful genotype-phenotype association in SCN1A-related infantile-onset epileptic encephalopathies
พ.ศ. 2560
Cholelithiasis in a Filipino child with chronic neuronopathic Gaucher disease: A case report
พ.ศ. 2560
Assessment of the Quality of Care of Patientswith Diabetic Emergencies Admittedin the Philippine General Hospital