Published in Acta Paediatr Taiwan on October 20, 2004
Extracorporeal membrane oxygenation rescue for cardiopulmonary resuscitation in pediatric patients. Crit Care Med (2008) 2.13
Anomalous brachiocephalic vein: CT, embryology, and clinical implications. AJR Am J Roentgenol (2005) 2.04
Eleven years of experience with extracorporeal cardiopulmonary resuscitation for paediatric patients with in-hospital cardiac arrest. Resuscitation (2012) 1.73
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
Genetic syndromes and outcome after surgical repair of pulmonary atresia and ventricular septal defect. Ann Thorac Surg (2012) 1.50
Kabuki syndrome in a girl with mosaic 45,X/47,XXX and aortic coarctation. Fertil Steril (2007) 1.42
Clinical implication of blood levels of B-type natriuretic peptide in pediatric patients on mechanical circulatory support. Ann Thorac Surg (2006) 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
Deletion of the C4-CYP21 repeat module leading to the formation of a chimeric CYP21P/CYP21 gene in a 9.3-kb fragment as a cause of steroid 21-hydroxylase deficiency. Clin Chem (2003) 1.41
Cholelithiasis in Down syndrome. Acta Paediatr Taiwan (2005) 1.39
Detection of chromosome aberrations during prenatal genetic testing for single gene disorders. Prenat Diagn (2004) 1.39
Scimitar syndrome: incidence, treatment, and prognosis. Eur J Pediatr (2007) 1.34
Two new susceptibility loci for Kawasaki disease identified through genome-wide association analysis. Nat Genet (2012) 1.30
Transcatheter arterial embolization of acute upper gastrointestinal tract bleeding with N-butyl-2-cyanoacrylate. J Vasc Interv Radiol (2007) 1.30
Unilateral lung agenesis--detrimental roles of surrounding vessels. Pediatr Pulmonol (2007) 1.16
Molecular genetic analysis of the TSC genes in two families with prenatally diagnosed rhabdomyomas. Prenat Diagn (2005) 1.15
Clinical characteristics and survival of trisomy 13 in a medical center in Taiwan, 1985-2004. Pediatr Int (2007) 1.15
Wolfram (DIDMOAD) syndrome: report of two patients. J Pediatr Endocrinol Metab (2004) 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
Mycotic aortic aneurysm presenting initially as an aortic intramural air pocket. AJR Am J Roentgenol (2005) 1.06
Mutation spectrum of MMACHC in Chinese patients with combined methylmalonic aciduria and homocystinuria. J Hum Genet (2010) 1.06
PCR-based detection of the CYP21 deletion and TNXA/TNXB hybrid in the RCCX module. Genomics (2004) 1.03
Analysis of genes encoding laminin beta2 and related proteins in patients with Galloway-Mowat syndrome. Pediatr Nephrol (2008) 1.02
Glomus tumor of the stomach: MRI findings. AJR Am J Roentgenol (2005) 1.02
A study of grid artifacts formation and elimination in computed radiographic images. J Digit Imaging (2006) 1.02
What is the correct depth of chest compression for infants and children? A radiological study. Pediatrics (2009) 1.00
Left pulmonary artery sling complex: computed tomography and hypothesis of embryogenesis. Ann Thorac Surg (2007) 0.99
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
Crossed pulmonary arteries: report of two cases with emphasis on three-dimensional helical computed tomographic imaging. J Formos Med Assoc (2008) 0.98
Stroke treatment in rats with tail temperature increase by 40-min moxibustion. Neurosci Lett (2011) 0.97
Double bubble sign. Emerg Med J (2011) 0.97
Characterization of pulmonary function impairments in patients with mucopolysaccharidoses--changes with age and treatment. Pediatr Pulmonol (2013) 0.97
Assessment of bone mineral density by dual energy x-ray absorptiometry in patients with mucopolysaccharidoses. Orphanet J Rare Dis (2013) 0.96
Long-term survival and unnatural deaths of patients with repaired tetralogy of Fallot in an Asian cohort. Circ Cardiovasc Qual Outcomes (2012) 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
CTLA-4 gene and susceptibility to human papillomavirus-16-associated cervical squamous cell carcinoma in Taiwanese women. Carcinogenesis (2007) 0.94
RUNX2 mutations in Taiwanese patients with cleidocranial dysplasia. Genet Mol Biol (2011) 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
Tumor necrosis factor-alpha promoter polymorphism is associated with susceptibility to oral squamous cell carcinoma. J Oral Pathol Med (2005) 0.92
Cerebral hemodynamic change and intraventricular hemorrhage in very low birth weight infants with patent ductus arteriosus. Ultrasound Med Biol (2005) 0.91
Clinical features of Ehlers-Danlos syndrome. J Formos Med Assoc (2006) 0.91
Prenatal sonographic findings of Klippel-Trénaunay-Weber syndrome. J Clin Ultrasound (2007) 0.91
Generalized arterial calcification of infancy: different clinical courses in two affected siblings. Am J Med Genet A (2005) 0.91
A systematic classification of the congenital bronchopulmonary vascular malformations: dysmorphogeneses of the primitive foregut system and the primitive aortic arch system. Yonsei Med J (2008) 0.91
Clinical and laboratory characteristics of type 1 diabetes in children and adolescents: experience from a medical center. Acta Paediatr Taiwan (2007) 0.90
Quality of life in adults with congenital heart disease: biopsychosocial determinants and sex-related differences. Heart (2010) 0.90
Characteristics of primary osteomyelitis among children in a medical center in Taipei, 1984-2002. J Formos Med Assoc (2005) 0.90
Polysomnographic characteristics in patients with mucopolysaccharidoses. Pediatr Pulmonol (2010) 0.90
HLA-DRB1 alleles and cervical squamous cell carcinoma: experimental study and meta-analysis. Hum Immunol (2006) 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
Rapid progressive course of later-onset Pompe disease in Chinese patients. Mol Genet Metab (2011) 0.89
Aortic valve prolapse associated with outlet-type ventricular septal defect. Ann Thorac Surg (2005) 0.88
Occlusion of an aberrant artery to an intralobar pulmonary sequestration using an Amplatzer Vascular Plug. Pediatr Pulmonol (2008) 0.88
Systemic anaphylaxis after the ingestion of pancake contaminated with the storage mite Blomia freemani. Ann Allergy Asthma Immunol (2005) 0.88
Pulmonary artery myxoma as a rare cause of dyspnea for a young female patient. J Thorac Cardiovasc Surg (2006) 0.88
Impact of glycemic control, disease duration, and exercise on heart rate variability in children with type 1 diabetes mellitus. J Formos Med Assoc (2007) 0.88
Enzyme replacement therapy for mucopolysaccharidosis VI--experience in Taiwan. J Inherit Metab Dis (2010) 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
Circulating matrix metalloproteinase-2 and -9 enzyme activities in the children with ventricular septal defect. Int J Biol Sci (2013) 0.87
Usefulness of three-dimensional electron beam computed tomography for evaluating tracheobronchial anomalies in children with congenital heart disease. Am J Cardiol (2003) 0.87
Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome. Ann Hum Genet (2009) 0.87
Congenital stridor and wheezing as harbingers of the del22q11.2 syndrome presenting cardiovascular malformations of right aortic arch, aberrant left subclavian artery, Kommerell's diverticulum, and left ligamentum arteriosum. Cardiovasc Pathol (2010) 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
Capturing phenotypic heterogeneity in MPS I: results of an international consensus procedure. Orphanet J Rare Dis (2012) 0.86
6p21.2-p12.3 deletion detected by aCGH in an 8-year-old girl with cleidocranial dysplasia and developmental delay. Gene (2013) 0.86
Perinatal imaging findings of inherited Sotos syndrome. Prenat Diagn (2002) 0.86
Experience with extracorporeal life support in pediatric patients after cardiac surgery. ASAIO J (2005) 0.86
ITPKC gene SNP rs28493229 and Kawasaki disease in Taiwanese children. Hum Mol Genet (2010) 0.86
Repair of complex tracheobronchial stenosis with left pulmonary artery sling and bridging bronchus. Ann Thorac Surg (2010) 0.85
Giant congenital left atrial aneurysm in an 11-year-old boy. Circulation (2012) 0.85
Disseminated Bacille Calmette-Guérin disease as the initial presentation of X-linked severe combined immunodeficiency--a case report. Asian Pac J Allergy Immunol (2005) 0.85
Circulating biomarkers of collagen type I metabolism mark the right ventricular fibrosis and adverse markers of clinical outcome in adults with repaired tetralogy of Fallot. Int J Cardiol (2012) 0.85
Magnetic resonance imaging of seminal vesicle cyst associated with ipsilateral urinary anomalies. J Formos Med Assoc (2006) 0.85
Array-CGH detection of a de novo 2.8 Mb deletion in 2q24.2-->q24.3 in a girl with autistic features and developmental delay. Eur J Med Genet (2010) 0.85
Interference and blood sample preparation for a pyruvate enzymatic assay. Clin Biochem (2005) 0.85
Outcomes in neonates with pulmonary atresia and intact ventricular septum underwent pulmonary valvulotomy and valvuloplasty using a flexible 2-French radiofrequency catheter. Yonsei Med J (2009) 0.85