PubRank

Sung Won Park

Author PubWeight™ 33.63‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Macrovesicular hepatic steatosis in living liver donors: use of CT for quantitative and qualitative assessment. Radiology 2006 3.02
2 Differentiation of extrahepatic bile duct cholangiocarcinoma from benign stricture: findings at MRCP versus ERCP. Radiology 2004 1.74
3 Serum cystatin C for estimation of residual renal function in children on peritoneal dialysis. Pediatr Nephrol 2010 1.49
4 Gastrointestinal metastasis from primary lung cancer: CT findings and clinicopathologic features. AJR Am J Roentgenol 2009 1.42
5 [The incidence and clinical features of Clostridium difficile infection; single center study]. Korean J Gastroenterol 2010 1.39
6 Another possible underlying mechanism for the positive association between celiac disease and systemic lupus erythematosus: the role of interleukin 21. J Rheumatol 2013 1.09
7 Bloodborne metastatic tumors to the gastrointestinal tract: CT findings with clinicopathologic correlation. AJR Am J Roentgenol 2006 0.99
8 Differential diagnosis of benign and malignant intraductal papillary mucinous tumors of the pancreas: MR cholangiopancreatography and MR angiography. Korean J Radiol 2003 0.98
9 Phase I/II clinical trial of enzyme replacement therapy with idursulfase beta in patients with mucopolysaccharidosis II (Hunter syndrome). Orphanet J Rare Dis 2013 0.93
10 Visceral adipose tissue is significantly associated with hearing thresholds in adult women. Clin Endocrinol (Oxf) 2013 0.91
11 Caveolin-1 and integrin β1 regulate embryonic stem cell proliferation via p38 MAPK and FAK in high glucose. J Cell Physiol 2011 0.87
12 Primary malignant melanoma of the rectum: CT findings in eight patients. Radiology 2004 0.87
13 Familial Xp22.33-Xp22.12 deletion delineated by chromosomal microarray analysis causes proportionate short stature. Am J Med Genet A 2012 0.86
14 Retrospective analysis of the clinical manifestations and survival of Korean patients with mucopolysaccharidosis type II: emphasis on the cardiovascular complication and mortality cases. Am J Med Genet A 2011 0.85
15 Mutations of ACADS gene associated with short-chain acyl-coenzyme A dehydrogenase deficiency. Ann Clin Lab Sci 2011 0.85
16 Clinical, biochemical, and genetic analysis of two korean patients with trichorhinophalangeal syndrome type I and growth hormone deficiency. Ann Clin Lab Sci 2012 0.84
17 Identification of signal peptide domain SOST mutations in autosomal dominant craniodiaphyseal dysplasia. Hum Genet 2011 0.84
18 A mother and daughter with the p.R443X mutation of mucopolysaccharidosis type II: Genotype and phenotype analysis. Am J Med Genet A 2010 0.83
19 High prevalence of carpal tunnel syndrome in children with mucopolysaccharidosis type II (Hunter syndrome). Am J Med Genet A 2011 0.83
20 Clinical, biochemical, and genetic analysis of korean patients with pseudohypoparathyroidism type Ia. Ann Clin Lab Sci 2010 0.82
21 Continuous renal replacement therapy in neonates weighing less than 3 kg. Korean J Pediatr 2012 0.81
22 Identification and in vivo functional characterization of novel compound heterozygous BMP1 variants in osteogenesis imperfecta. Hum Mutat 2015 0.80
23 Five novel mutations of GALNS in Korean patients with mucopolysaccharidosis IVA. Am J Med Genet A 2013 0.80
24 Two novel insulin receptor gene mutations in a patient with Rabson-Mendenhall syndrome: the first Korean case confirmed by biochemical, and molecular evidence. J Korean Med Sci 2012 0.80
25 Correlation of adiponectin receptor expression with cytokines and insulin sensitivity in growth hormone (GH)-treated children with Prader-Willi syndrome and in non-GH-treated obese children. J Clin Endocrinol Metab 2010 0.79
26 Auditory characteristics and therapeutic effects of enzyme replacement in mouse model of the mucopolysaccharidosis (MPS) II. Am J Med Genet A 2012 0.78
27 Enzyme replacement therapy improves joint motion and outcome of the 12-min walk test in a mucopolysaccharidosis type VI patient previously treated with bone marrow transplantation. Am J Med Genet A 2012 0.78
28 The metabolic syndrome and body composition in childhood cancer survivors. Korean J Pediatr 2011 0.77
29 A study of the relationship between clinical phenotypes and plasma iduronate-2-sulfatase enzyme activities in Hunter syndrome patients. Korean J Pediatr 2012 0.77
30 Two novel PEX1 mutations in a patient with Zellweger syndrome: the first Korean case confirmed by biochemical, and molecular evidence. Ann Clin Lab Sci 2011 0.77
31 A Korean patient with Morquio B disease with a novel c.13_14insA mutation in the GLB1 gene. Ann Clin Lab Sci 2012 0.77
32 Genotyping of CYP21A2 for congenital adrenal hyperplasia screening using allele-specific primer extension followed by bead array hybridization. Mol Diagn Ther 2009 0.76
33 Chronic peritoneal dialysis in a 4-year-old boy with Lesch-Nyhan disease. Pediatr Nephrol 2008 0.76
34 Diagnosis and constitutional and laboratory features of Korean girls referred for precocious puberty. Korean J Pediatr 2012 0.75
35 Delayed response of amylin levels after an oral glucose challenge in children with Prader-Willi syndrome. Yonsei Med J 2011 0.75
36 [A case of intraductal papillary mucinous neoplasm of the pancreas arising from pancreas divisum without ventral pancreatic duct of Wirsung]. Korean J Gastroenterol 2006 0.75
37 Risk factors of missed colorectal lesions after colonoscopy. Medicine (Baltimore) 2017 0.75
38 Extracorporeal Shockwave Therapy in Patients with Morton's Neuroma A Randomized, Placebo-Controlled Trial. J Am Podiatr Med Assoc 2016 0.75