Published in Prenat Diagn on October 01, 2002
Genetic considerations in the prenatal diagnosis of overgrowth syndromes. Prenat Diagn (2009) 1.38
Sotos syndrome. Orphanet J Rare Dis (2007) 1.12
Sonographic prenatal diagnosis of central nervous system abnormalities. Childs Nerv Syst (2003) 1.08
Assessment of fetal intracranial pathologies first demonstrated late in pregnancy: cell proliferation disorders. Reprod Biol Endocrinol (2003) 0.76
Childhood soft-tissue sarcoma associated with Sotos syndrome. Radiol Case Rep (2015) 0.75
Region-specific changes in brain diffusivity in fetal isolated mild ventriculomegaly. Eur Radiol (2015) 0.75
mTORC1 promotes survival through translational control of Mcl-1. Proc Natl Acad Sci U S A (2008) 2.50
The effect of in-hospital developmental care on neonatal morbidity, growth and development of preterm Taiwanese infants: a randomized controlled trial. Early Hum Dev (2012) 1.98
Targeting histone deacetylase in cancer therapy. Med Res Rev (2006) 1.69
Incidence of the mucopolysaccharidoses in Taiwan, 1984-2004. Am J Med Genet A (2009) 1.67
Efficacy and safety of enzyme replacement therapy with BMN 110 (elosulfase alfa) for Morquio A syndrome (mucopolysaccharidosis IVA): a phase 3 randomised placebo-controlled study. J Inherit Metab Dis (2014) 1.60
The Morquio A Clinical Assessment Program: baseline results illustrating progressive, multisystemic clinical impairments in Morquio A subjects. Mol Genet Metab (2013) 1.57
NEMO gene mutations in Chinese patients with incontinentia pigmenti. J Formos Med Assoc (2010) 1.51
Second-trimester diagnosis of complete trisomy 9 associated with abnormal maternal serum screen results, open sacral spina bifida and congenital diaphragmatic hernia, and review of the literature. Prenat Diagn (2004) 1.46
Carbon monoxide poisoning in children. Pediatr Neonatol (2008) 1.45
Usefulness of magnetic resonance cholangiopancreatography in pancreatobiliary abnormalities in pediatric patients. Pediatr Neonatol (2011) 1.45
Prenatal diagnosis of mosaic distal 5p deletion and review of the literature. Prenat Diagn (2004) 1.44
Kabuki syndrome in a girl with mosaic 45,X/47,XXX and aortic coarctation. Fertil Steril (2007) 1.42
Prevalence of Helicobacter pylori infection in high-school students on Lanyu Island, Taiwan: risk factor analysis and effect on growth. J Formos Med Assoc (2009) 1.42
Clinical characteristics and survival of trisomy 18 in a medical center in Taipei, 1988-2004. Am J Med Genet A (2006) 1.41
Prenatal diagnosis of mosaic trisomy 16 associated with congenital diaphragmatic hernia and elevated maternal serum alpha-fetoprotein and human chorionic gonadotrophin. Prenat Diagn (2004) 1.41
Detection of chromosome aberrations during prenatal genetic testing for single gene disorders. Prenat Diagn (2004) 1.39
A psychometric study of the Bayley Scales of Infant and Toddler Development - 3rd Edition for term and preterm Taiwanese infants. Res Dev Disabil (2013) 1.36
Two new susceptibility loci for Kawasaki disease identified through genome-wide association analysis. Nat Genet (2012) 1.30
Right perinephric abscess: a rare presentation of ruptured retrocecal appendicitis. Pediatr Nephrol (2002) 1.26
Neonatal sepsis in the neonatal intensive care unit: characteristics of early versus late onset. J Microbiol Immunol Infect (2004) 1.23
Clinical features and prognostic factors in childhood pneumococcal meningitis. J Microbiol Immunol Infect (2008) 1.17
Molecular genetic analysis of the TSC genes in two families with prenatally diagnosed rhabdomyomas. Prenat Diagn (2005) 1.15
National survey of invasive pneumococcal diseases in Taiwan under partial PCV7 vaccination in 2007: emergence of serotype 19A with high invasive potential. Vaccine (2009) 1.15
Clinical characteristics and survival of trisomy 13 in a medical center in Taiwan, 1985-2004. Pediatr Int (2007) 1.15
Prenatal diagnosis of pentalogy of Cantrell associated with hypoplasia of the right upper limb and ectrodactyly. Prenat Diagn (2007) 1.12
Infections associated with indwelling ventriculostomy catheters in a teaching hospital. Int J Infect Dis (2009) 1.09
Bronchopulmonary dysplasia predicts adverse developmental and clinical outcomes in very-low-birthweight infants. Dev Med Child Neurol (2008) 1.09
Identification of novel susceptibility Loci for kawasaki disease in a Han chinese population by a genome-wide association study. PLoS One (2011) 1.08
Neonatal Morganella morganii sepsis: a case report and review of the literature. Pediatr Int (2011) 1.07
Concomitant rotavirus and Salmonella infections in children with acute diarrhea. Pediatr Neonatol (2009) 1.06
Mutation spectrum of MMACHC in Chinese patients with combined methylmalonic aciduria and homocystinuria. J Hum Genet (2010) 1.06
Analysis of genes encoding laminin beta2 and related proteins in patients with Galloway-Mowat syndrome. Pediatr Nephrol (2008) 1.02
High cytomegalovirus load and prolonged virus excretion in breast milk increase risk for viral acquisition by very low birth weight infants. Pediatr Infect Dis J (2009) 0.99
Prevalence, detection and treatment of delirium in terminal cancer inpatients: a prospective survey. Jpn J Clin Oncol (2008) 0.98
Subdural empyema in children--20-year experience in a medical center. J Microbiol Immunol Infect (2008) 0.98
Enzyme assay and clinical assessment in subjects with a Chinese hotspot late-onset Fabry mutation (IVS4 + 919G→A). J Inherit Metab Dis (2010) 0.98
Diffuse xanthogranulomatous pyelonephritis in a child with severe complications. Pediatr Nephrol (2004) 0.96
Transmission of cytomegalovirus from mothers to preterm infants by breast milk. Pediatr Infect Dis J (2004) 0.96
Assessment of bone mineral density by dual energy x-ray absorptiometry in patients with mucopolysaccharidoses. Orphanet J Rare Dis (2013) 0.96
Viral etiology of acute lower respiratory tract infections in hospitalized young children in Northern Taiwan. J Microbiol Immunol Infect (2011) 0.95
Outcome of pregnancy in patients with systemic lupus erythematosus. Taiwan J Obstet Gynecol (2006) 0.95
Effects of growth hormone treatment on height, weight, and obesity in Taiwanese patients with Prader-Willi syndrome. J Chin Med Assoc (2008) 0.95
Serum cytokines in differentiating between viral and bacterial enterocolitis. Ann Trop Paediatr (2004) 0.94
Severity of bronchopulmonary dysplasia and increased risk of feeding desaturation and growth delay in very low birth weight preterm infants. Pediatr Pulmonol (2010) 0.93
Ceftriaxone resistance of nontyphoidal Salmonella enterica isolates in Northern Taiwan attributable to production of CTX-M-14 and CMY-2 beta-lactamases. J Clin Microbiol (2005) 0.93
RUNX2 mutations in Taiwanese patients with cleidocranial dysplasia. Genet Mol Biol (2011) 0.93
Case report. CT diagnosis of volvulus of the descending colon with persistent mesocolon. AJR Am J Roentgenol (2003) 0.93
Prenatal diagnosis of the Dandy-Walker malformation and ventriculomegaly associated with partial trisomy 9p and distal 12p deletion. Prenat Diagn (2002) 0.93
Plasma globotriaosylsphingosine (lysoGb3) could be a biomarker for Fabry disease with a Chinese hotspot late-onset mutation (IVS4+919G>A). Clin Chim Acta (2013) 0.92
Factors for poor prognosis of neonatal bacterial meningitis in a medical center in Northern Taiwan. J Microbiol Immunol Infect (2012) 0.92
Cerebral hemodynamic change and intraventricular hemorrhage in very low birth weight infants with patent ductus arteriosus. Ultrasound Med Biol (2005) 0.91
Generalized arterial calcification of infancy: different clinical courses in two affected siblings. Am J Med Genet A (2005) 0.91
Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy. Taiwan J Obstet Gynecol (2011) 0.91
Clinical features of Ehlers-Danlos syndrome. J Formos Med Assoc (2006) 0.91
Congenital cystic adenomatoid malformation in twin-twin transfusion syndrome: fetal MR imaging. Pediatr Radiol (2007) 0.91
Prenatal sonographic findings of Klippel-Trénaunay-Weber syndrome. J Clin Ultrasound (2007) 0.91
Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction. Taiwan J Obstet Gynecol (2011) 0.90
Typical body wall defect associated with craniofacial anomalies and amniotic bands diagnosed in early pregnancy. Taiwan J Obstet Gynecol (2007) 0.90
Scrub typhus in children in a teaching hospital in eastern Taiwan, 2000-2005. Southeast Asian J Trop Med Public Health (2009) 0.90
Unbalanced reciprocal translocations at amniocentesis. Taiwan J Obstet Gynecol (2011) 0.90
Characteristics of primary osteomyelitis among children in a medical center in Taipei, 1984-2002. J Formos Med Assoc (2005) 0.90
Chromosome 17p13.3 deletion syndrome: aCGH characterization, prenatal findings and diagnosis, and literature review. Gene (2013) 0.90
Fetal cystic lung lesions: evaluation with magnetic resonance imaging. Pediatr Pulmonol (2010) 0.90
Polysomnographic characteristics in patients with mucopolysaccharidoses. Pediatr Pulmonol (2010) 0.90
Contribution of ultrafast magnetic resonance imaging in prenatal diagnosis of sonographically undetected cerebral tuberous sclerosis associated with cardiac rhabdomyomas. Prenat Diagn (2005) 0.89
Concomitant exencephaly and limb defects associated with pentalogy of Cantrell. Taiwan J Obstet Gynecol (2008) 0.89
Rapid progressive course of later-onset Pompe disease in Chinese patients. Mol Genet Metab (2011) 0.89
Congenital lobar emphysema: appearance on fetal MRI. Pediatr Radiol (2008) 0.89
Clinical manifestations, laboratory findings and complications of pediatric scrub typhus in eastern Taiwan. Pediatr Neonatol (2009) 0.88
Enzyme replacement therapy for mucopolysaccharidosis VI--experience in Taiwan. J Inherit Metab Dis (2010) 0.88
Comparison of the characteristics of culture-negative versus culture-positive septic arthritis in children. J Microbiol Immunol Infect (2005) 0.88
Infected cephalohematoma of newborns: experience in a medical center in Taiwan. Pediatr Int (2005) 0.88
Osteogenesis imperfecta type IV: prenatal molecular diagnosis and genetic counseling in a pregnancy carried to full term with favorable outcome. Taiwan J Obstet Gynecol (2012) 0.88
Renal sonographic findings of type I glycogen storage disease in infancy and early childhood. Pediatr Radiol (2005) 0.87
Pulmonary venous aneurysm mimicking a right infrahilar tumour. Eur J Cardiothorac Surg (2012) 0.87
Prenatal diagnosis of concomitant alobar holoprosencephaly and caudal regression syndrome associated with maternal diabetes. Prenat Diagn (2005) 0.87
Characterization of a de novo unbalanced Y;autosome translocation in a 45,X mentally retarded male and literature review. Fertil Steril (2008) 0.87
Molecular diagnosis of a novel heterozygous 268C-->T (R90C) mutation in TGIF gene in a fetus with holoprosencephaly and premaxillary agenesis. Prenat Diagn (2002) 0.87
Short rib-polydactyly syndrome type II (Majewski): prenatal diagnosis, perinatal imaging findings and molecular analysis of the NEK1 gene. Taiwan J Obstet Gynecol (2012) 0.87
Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome. Ann Hum Genet (2009) 0.87