Published in Pediatr Res on October 01, 2002
Link between colorectal cancer and polymorphisms in the uridine-diphosphoglucuronosyltransferase 1A7 and 1A1 genes. World J Gastroenterol (2005) 0.98
Association of Neonatal Hyperbilirubinemia with UGT1A1 Gene Polymorphisms: A Meta-Analysis. Med Sci Monit (2015) 0.87
UGT1A1 sequence variants and bilirubin levels in early postnatal life: a quantitative approach. BMC Med Genet (2011) 0.86
Relation between Neonatal Icter and Gilbert Syndrome in Gloucose-6-Phosphate Dehydrogenase Deficient Subjects. J Clin Diagn Res (2014) 0.83
Polymorphisms of uridine-diphosphoglucuronosyltransferase 1A7 gene in Taiwan Chinese. World J Gastroenterol (2005) 0.80
Multiple Genetic Modifiers of Bilirubin Metabolism Involvement in Significant Neonatal Hyperbilirubinemia in Patients of Chinese Descent. PLoS One (2015) 0.78
Crigler-Najjar syndrome type II in a Chinese boy resulting from three mutations in the bilirubin uridine 5'-diphosphate-glucuronosyltransferase (UGT1A1) gene and a family genetic analysis. BMC Pediatr (2014) 0.76
Association of UGT1A1 variants and hyperbilirubinemia in breast-fed full-term Chinese infants. PLoS One (2014) 0.76
Neonatal indirect hyperbilirubinemia and glucose-6-phosphate dehydrogenase deficiency. Korean J Pediatr (2017) 0.75
Effects of variant UDP-glucuronosyltransferase 1A1 gene, glucose-6-phosphate dehydrogenase deficiency and thalassemia on cholelithiasis. World J Gastroenterol (2005) 0.75
Multiple variants in UGT1A1 gene are factors to develop indirect hyper-bilirubinemia. Hepatobiliary Surg Nutr (2014) 0.75
Risk assessment of gene variants for neonatal hyperbilirubinemia in Taiwan. BMC Pediatr (2016) 0.75
The Association between Prolonged Jaundice and UGT1A1 Gene Polymorphism (G71R) in Gilbert's Syndrome. J Clin Diagn Res (2016) 0.75
Hepatic expression of transcription factors affecting developmental regulation of UGT1A1 in the Han Chinese population. Eur J Clin Pharmacol (2016) 0.75
A common variant in the PNPLA3 gene is a risk factor for non-alcoholic fatty liver disease in obese Taiwanese children. J Pediatr (2010) 1.60
Determination of brain death in children--a medicial center experience. Acta Paediatr Taiwan (2005) 1.43
Handwashing program for the prevention of nosocomial infections in a neonatal intensive care unit. Infect Control Hosp Epidemiol (2004) 1.08
Genetic variants in GCKR and PNPLA3 confer susceptibility to nonalcoholic fatty liver disease in obese individuals. Am J Clin Nutr (2014) 1.06
Genetic factors related to unconjugated hyperbilirubinemia amongst adults. Pharmacogenet Genomics (2005) 1.04
Glucose-6-phosphate dehydrogenase deficiency, the UDP-glucuronosyl transferase 1A1 gene, and neonatal hyperbilirubinemia. Gastroenterology (2002) 1.01
Relationship between spontaneous kicking and age of walking attainment in preterm infants with very low birth weight and full-term infants. Phys Ther (2004) 0.98
Brief report: Taiwanese infants' mental and motor development--6-24 months. J Pediatr Psychol (2007) 0.94
Congenital midline nasal mass: cases series and review of the literature. Turk J Pediatr (2011) 0.93
Risk factors for liver steatosis in obese children and adolescents. Pediatr Neonatol (2010) 0.92
Variants in the UGT1A1 gene and the risk of pediatric nonalcoholic fatty liver disease. Pediatrics (2009) 0.90
Necrotizing enterocolitis complicated with perforation in extremely low birth-weight premature infants. Acta Paediatr Taiwan (2002) 0.89
Distribution of HLA-DQB1 alleles in patients with Kleine-Levin syndrome. J Clin Neurosci (2012) 0.87
Preeclampsia and the risk of bronchopulmonary dysplasia in VLBW infants: a population based study. PLoS One (2013) 0.86
A common variant in the peroxisome proliferator-activated receptor-γ coactivator-1α gene is associated with nonalcoholic fatty liver disease in obese children. Am J Clin Nutr (2012) 0.86
Predictive value of clinical features in differentiating group A beta-hemolytic streptococcal pharyngitis in children. J Microbiol Immunol Infect (2003) 0.85
Delivery before 32 weeks of gestation for maternal pre-eclampsia: neonatal outcome and 2-year developmental outcome. Early Hum Dev (2004) 0.85
Crigler-Najjar syndrome type 2. J Formos Med Assoc (2006) 0.85
Coinheritance of variant UDP-glucuronosyl transferase 1A1 gene and glucose-6-phosphate dehydrogenase deficiency in adults with hyperbilirubinemia. Pharmacogenetics (2002) 0.84
Variations in the UDP-glucuronosyltransferase 1A1 gene for the development of unconjugated hyperbilirubinemia in Taiwanese. Pharmacogenomics (2008) 0.84
UDP-glucuronosyltransferase 1A7 polymorphisms are associated with liver cirrhosis. Biochem Biophys Res Commun (2007) 0.83
When a problem-based learning tutor decides to intervene. Acad Med (2009) 0.83
Unambiguous molecular detections with multiple genetic approach for the complicated chromosome 22q11 deletion syndrome. BMC Med Genet (2009) 0.82
Developmental function of very-low-birth-weight infants and full-term infants in early childhood. J Formos Med Assoc (2004) 0.81
Relationship between perinatal and neonatal indices and intelligence quotient in very low birth weight infants at the age of 6 or 8 years. Pediatr Neonatol (2008) 0.80
Epidemiological and clinical features of group A Streptococcus pharyngitis in children. Acta Paediatr Taiwan (2004) 0.80
Auditory event-related potentials in children with attention deficit hyperactivity disorder. Pediatr Neonatol (2012) 0.79
Esophageal atresia associated with tracheal stenosis and right lung agenesis: report of one case. Acta Paediatr Taiwan (2003) 0.79
Spontaneous spinal epidural hematoma in a 5-year-old girl. Acta Paediatr Taiwan (2003) 0.78
Age-changed normative auditory event-related potential value in children in Taiwan. J Formos Med Assoc (2012) 0.78
Variations of movement disorders in anti-N-methyl-D-aspartate receptor encephalitis: A nationwide study in Taiwan. Medicine (Baltimore) (2016) 0.77
The thrombopoietin level in the cord blood in premature infants born to mothers with pregnancy-induced hypertension. Biol Neonate (2002) 0.77
Longitudinal follow-up of lymphocyte subsets during the first year of life. Asian Pac J Allergy Immunol (2002) 0.77
A vitronectin M381T polymorphism increases risk of hemangioblastoma in patients with VHL gene defect. J Mol Med (Berl) (2009) 0.76
Analysis of double-stranded DNA by microchip capillary electrophoresis using polymer solutions containing gold nanoparticles. J Chromatogr A (2003) 0.76
Pallister-Killian syndrome: report of one case. Acta Paediatr Taiwan (2006) 0.76
Vagus nerve stimulation therapy in pediatric epilepsy: current understanding and future directions. Pediatr Neonatol (2012) 0.75
Effects of variant UDP-glucuronosyltransferase 1A1 gene, glucose-6-phosphate dehydrogenase deficiency and thalassemia on cholelithiasis. World J Gastroenterol (2005) 0.75
Bilateral central retinal vein occlusion with multiple intracerebral hemorrhage in a neonate. Pediatr Neurol (2003) 0.75
Umbilical vein catheter malposition: report of one case. Acta Paediatr Taiwan (2003) 0.75
Bilirubin concentrations in thalassemia heterozygotes in university students. Eur J Haematol (2011) 0.75
A patient with PHACE syndrome with marked ipsilateral cerebral atrophy. Pediatr Neonatol (2010) 0.75
Prolonged Hyperbilirubinemia in a Neonate with a Novel Mutation in the UDP-glucuronosyltransferase 1A1 Gene. Neonatology (2016) 0.75
Cognitive development at age 8 years in very low birth weight children in Taiwan. J Formos Med Assoc (2008) 0.75
Mortality, disability, and intensive care in patients with mitochondrial 3243A>G mutation. Intensive Care Med (2015) 0.75
Is medical students' moral orientation changeable after preclinical medical education? J Med Ethics (2011) 0.75
Group B streptococcus infection in infancy: 21-year experience. Acta Paediatr Taiwan (2003) 0.75
Outcome of very low birth weight infants with sonographic enlarged occipital horn. Pediatr Neurol (2004) 0.75
Novel human pathological mutations. Gene symbol: NF1. Disease: neurofibromatosis 1. Hum Genet (2007) 0.75
Neonatal outcome of infants born after in vitro fertilization at National Taiwan University Hospital. J Formos Med Assoc (2002) 0.75
Gastric Anatomic Type Is Associated with Obesity and Gender. Obes Facts (2016) 0.75