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Molecular signatures for the class Coriobacteriia and its different clades; proposal for division of the class Coriobacteriia into the emended order Coriobacteriales, containing the emended family
The species of the class Coriobacteriia are currently distinguished from other bacteria primarily on the basis of their branching in the 16S rRNA gene trees. No reliable molecular marker is knownExpand
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Comparison of the efficacy of triple versus quadruple therapy on the eradication of Helicobacter pylori and antibiotic resistance
OBJECTIVE:  Our aim was to compare the efficacy and safety of Helicobacter pylori (H. pylori) eradication with pantoprazole‐based 7‐day standard triple therapy (PAC) and 10‐day quadruple therapyExpand
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Hypertriglyceridemic acute pancreatitis in emergency department: Typical clinical features and genetic variants
To investigate the clinical characteristics of patients with hypertriglyceridemic acute pancreatitis (HTGAP), and the molecular foundation contributing to hypertriglyceridemia in such patients.
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Low FT3 is a valuable predictor of severe acute pancreatitis in the emergency department
To investigate the relationship between serum levels of thyroid hormones and disease severity at the early stage of acute pancreatitis (AP).
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Comparison of three scoring systems in predicting clinical outcomes in patients with acute upper gastrointestinal bleeding: a prospective observational study
To compare the performances of the Glasgow‐Blatchford score (GBS), modified GBS (mGBS) and AIMS65 in predicting clinical outcomes in patients with acute upper gastrointestinal bleeding (AUGIB).
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The evaluation of the efficacy of pantoprazole-based triple and quadruple therapy in Helicobacter pylori eradication
Objective Compare the efficacy and safety of pantoprazole-based 7-day standard triple therapy with 10-day quadruple therapy including pantoprazole, bismuth, metronidazole and tetracycline inExpand
Postmortem diagnosis of sitosterolaemia by next-generation sequencing in a patient with severe hypercholesterolaemia and cardiovascular failure
Abstract Background and aims Sitosterolaemia (STSL; OMIN #210250) is a disorder of lipid metabolism and a rare autosomal recessive condition caused by loss-of-function biallelic mutations in theExpand