Search Results - "JEONG KEE SEO"
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Very early-onset inflammatory bowel disease (IBD) in infancy is a different disease entity from adult-onset IBD; one form of interleukin-10 receptor mutations
Published in Journal of human genetics (01-06-2014)“…Infantile periods may have stronger genetic influences. Recently, studies on genetic defects in the interleukin-10 (IL-10) signaling pathway have provided new…”
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2
Pyrosequencing‐based Molecular Monitoring of the Intestinal Bacterial Colonization in Preterm Infants
Published in Journal of pediatric gastroenterology and nutrition (01-11-2011)“…ABSTRACT Objectives: The aim of the study was to investigate the previously unexplored diversity of neonatal intestinal microbiota and monitor early intestinal…”
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3
Lactobacillus plantarum inhibits epithelial barrier dysfunction and interleukin-8 secretion induced by tumor necrosis factor-α
Published in World journal of gastroenterology : WJG (07-04-2007)“…AIM: To determine whether Lactobacillus plantarum can modify the deleterious effects of tumor necrosis factor-α (TNF-α) on intestinal epithelial cells…”
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4
Hepatic arterial diameter measured with US: adjunct for US diagnosis of biliary atresia
Published in Radiology (01-11-2007)“…To prospectively evaluate the accuracy of hepatic artery diameter and hepatic artery diameter-to-portal vein diameter ratio for ultrasonographic (US) diagnosis…”
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5
Abatacept alleviates severe autoimmune symptoms in a patient carrying a de novo variant in CTLA-4
Published in Journal of allergy and clinical immunology (01-01-2016)“…Notably, there was a recent case report on abatacept treatment in an adult with idiopathic autoimmune enteropathy.7 To investigate the molecular effect of the…”
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6
cagA, vacA, and iceA genotypes of Helicobacter pylori in Korean children
Published in Pediatrics international (01-10-2008)“…Background: Several putative virulence factors for Helicobacter pylori have been identified including cagA, vacA, and iceA. The aims of the present study were…”
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7
The Usefulness of Distal Splenorenal Shunt in Children with Portal Hypertension for the Treatment of Severe Thrombocytopenia and Leukopenia
Published in World journal of surgery (01-03-2008)“…Background In the current era of transplantation and therapeutic endoscopy, the role of the distal splenorenal shunt (DSRS) for portal hypertension (PH) has…”
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8
Small anellovirus infections in Korean children
Published in Emerging infectious diseases (01-05-2007)Get full text
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9
Development of Hepatocellular Carcinoma in Patients with Glycogen Storage Disease: a Single Center Retrospective Study
Published in Journal of Korean medical science (06-01-2020)“…Glycogen storage disease (GSD) is an inherited disorder leading to abnormal glucose metabolism and glycogen accumulation, and is associated with various…”
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10
Independent Introduction of Two Lactase-Persistence Alleles into Human Populations Reflects Different History of Adaptation to Milk Culture
Published in American journal of human genetics (01-01-2008)“…The T −13910 variant located in the enhancer element of the lactase ( LCT) gene correlates perfectly with lactase persistence (LP) in Eurasian populations…”
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11
Diagnosis of Wilson disease in young children: molecular genetic testing and a paradigm shift from the laboratory diagnosis
Published in Pediatric gastroenterology, hepatology & nutrition (01-12-2012)“…Wilson disease (WD) is an autosomal recessive disorder of copper metabolism that results in accumulation of copper primarily in the liver, brain and cornea…”
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12
Clinical and ABCB11 profiles in Korean infants with progressive familial intrahepatic cholestasis
Published in World journal of gastroenterology : WJG (28-05-2016)“…AIM: To investigate clinical profiles and mutations of ABCB11 in Koreans with progressive familial intrahepatic cholestasis 2 and review the differences…”
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13
Review : Intestinal Neuronal Dysplasia
Published in The Korean journal of gastroenterology (30-08-2007)“…Intestinal neuronal dysplasia (IND) type B is a disease of the submucosal plexus of intestine manifesting chronic intestinal obstruction or severe chronic…”
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14
Correlations of Plasma Citrulline Levels With Clinical and Endoscopic Score and Blood Markers According to Small Bowel Involvement in Pediatric Crohn Disease
Published in Journal of pediatric gastroenterology and nutrition (01-11-2013)“…ABSTRACT Objective: Several studies have indicated that plasma citrulline levels reflect the extent of mucosal injury of the small intestine. This study was…”
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15
해설논문(Review Article) : 윌슨병: 진단과 치료의 최근 동향
Published in Clinical and molecular hepatology (25-09-2006)“…Wilson disease (WD) is an autosomal recessive disorder of copper transport that results in accumulation of copper primarily in the liver, the brain and the…”
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16
Overview of rotavirus infections in Korea
Published in Pediatrics international (01-08-2000)“…Rotavirus is the most common cause of acute watery diarrhea in young Korean children. Rotavirus vaccine will soon be available, and information is urgently…”
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Histopathology and expression of Ki-67 and cyclooxygenase-2 in childhood Helicobacter pylori gastritis
Published in Journal of gastroenterology (01-03-2004)“…Helicobacter pylori infection has been implicated in many pathobiologic changes that are linked with the pathogenesis of gastric cancer. The majority of…”
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18
Clinical features of congenital portosystemic shunt in children
Published in European journal of pediatrics (01-02-2012)“…Clinical features, images, complications, treatments, and prognosis of 10 children with congenital portosystemic shunt (CPSS) were reviewed. Nine children were…”
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Helicobacter pylori Stool Antigen (HpSA) Tests in Children Before and After Eradication Therapy: Comparison of Rapid Immunochromatographic Assay and HpSA ELISA
Published in Digestive diseases and sciences (01-08-2008)“…The rapid immunochromatography for Helicobacter pylori ( H. pylori ) stool antigen (rapid HpSA) test is a recently-developed method for detection of H. pylori…”
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20
Germline Mutation Analysis of STK11 Gene Using Direct Sequencing and Multiplex Ligation-Dependent Probe Amplification Assay in Korean Children with Peutz-Jeghers Syndrome
Published in Digestive diseases and sciences (01-12-2010)“…Background and Aims Peutz-Jeghers syndrome is an autosomal, dominantly inherited disease characterized by mucocutaneous hyperpigmentation and hamartomatous…”
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