Yonggeng Jiao

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Wilson Disease (WD) is an inborn error of copper metabolism inherited in an autosomal recessive manner caused by the mutations in the P-type ATPase gene (ATP7B). In this study, we screen and detect the mutations of the ATP7B gene in unrelated Chinese WD patients. A total of 68 individuals from ten provinces of China with WD were recruited. Of them, 43 were(More)
OBJECTIVE A randomized controlled trial to evaluate the use of fat emulsion and normal saline for bile leakage tests during hepatic resection. METHODS Patients were randomized to undergo intraoperative bile leakage tests with saline then fat emulsion (Group A), or fat emulsion then saline (Group B). All patients received both tests. RESULTS In group A(More)
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