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Oct 21, 2017 (publication date) through Nov 30, 2024
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Publication Name
World Journal of Gastroenterology
ISSN
1007-9327
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Zhou Y, Jiang M, Tang ST, Yang L, Zhang X, Yang DH, Xiong M, Li S, Cao GQ, Wang Y. Laparoscopic finding of a hepatic subcapsular spider-like telangiectasis sign in biliary atresia. World J Gastroenterol 2017; 23(39): 7119-7128 [PMID: 29093620 DOI: 10.3748/wjg.v23.i39.7119] |
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| URL: | https://www.wjgnet.com/1007-9327/full/v23/i39/7119.htm |
| Number | Citing Articles |
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Jing Ye, Dengming Lai, Dan Cao, Linhua Tan, Lei Hu, Hua Zha, Jiezuan Yang, Qiang Shu. Altered T-Cell Receptor β-Chain and Lactate Dehydrogenase Are Associated With the Immune Pathogenesis of Biliary Atresia. Frontiers in Medicine 2021; 8 doi: 10.3389/fmed.2021.778500
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Jianghua Zhan, Shaowen Liu, Yu Meng, Qianhui Yang, Zhiru Wang, Shujian Zhang, Liang Ge, Li Zhao, Xiaodan Xu, Yilin Zhao, Xin Li, Xueting Wang. Systematic review of the mechanism and assessment of liver fibrosis in biliary atresia. Pediatric Surgery International 2024; 40(1) doi: 10.1007/s00383-024-05778-x
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Yibo Li, Liying Rong, Jingfeng Tang, Huizhong Niu, Zhu Jin, Yun Zhou, Guoqing Cao, Xi Zhang, Shuiqing Chi, Shaotao Tang. Re-evaluation of Laparoscopic Hepatic Subcapsular Spider-Like Telangiectasis Sign: A Highly Accurate Method to Diagnose Biliary Atresia in Infants. Frontiers in Pediatrics 2022; 10 doi: 10.3389/fped.2022.850449
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Patrícia Quelhas, Carlos Cerski, Jorge Luiz dos Santos. Update on Etiology and Pathogenesis of Biliary Atresia. Current Pediatric Reviews 2023; 19(1): 48 doi: 10.2174/1573396318666220510130259
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Xiaopan Chang, Shuiqing Chi, Xi Zhang, Xiangyang Li, Cheng Yu, Ying Zhou, Shaotao Tang. Inhibition of Notch3/Hey1 ameliorates peribiliary hypoxia by preventing hypertrophic hepatic arteriopathy in biliary atresia progression. Histochemistry and Cell Biology 2024; 161(6): 461 doi: 10.1007/s00418-024-02278-w
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| 6 |
Vincenzo Carollo, Mariapina Milazzo, Roberto Miraglia. The “hepatic subcapsular flow sign” in early diagnosis of biliary atresia. Abdominal Radiology 2019; 44(9): 3200 doi: 10.1007/s00261-019-02115-y
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Jinfeng Zhao, Xiaodan Xu, Qingyun Gou, Qipeng Zheng, Liang Ge, Lingzhi Chen, Cong Zhang, Hui Ma, Shuxiang Lin, Xiaoli Hu, Jianghua Zhan. TGF-β1-Mediated Leukocyte Cell-Derived Chemotaxin 2 Is Associated With Liver Fibrosis in Biliary Atresia. Frontiers in Pediatrics 2022; 10 doi: 10.3389/fped.2022.901888
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Mengxin Zhang, Guoqing Cao, Xiangyang Li, Xi Zhang, Yibo Li, Shuiqing Chi, Liying Rong, Shao-tao Tang. Robotic-assisted Kasai portoenterostomy for biliary atresia. Surgical Endoscopy 2023; 37(5): 3540 doi: 10.1007/s00464-022-09855-x
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Patricia Quelhas, Joana Jacinto, Carlos Cerski, Rui Oliveira, Jorge Oliveira, Elisa Carvalho, Jorge dos Santos. Protocols of Investigation of Neonatal Cholestasis—A Critical Appraisal. Healthcare 2022; 10(10): 2012 doi: 10.3390/healthcare10102012
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| 10 |
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Patrícia Quelhas, Michele Claire Breton, Rui Caetano Oliveira, Maria Augusta Cipriano, Paulo Teixeira, Carlos Thadeu Cerski, Pranavkumar Shivakumar, Sandra Maria Gonçalves Vieira, Carlos Oscar Kieling, Ignacio Verde, Jorge Luiz dos Santos. HIF-1alpha-pathway activation in cholangiocytes of patients with biliary atresia: An immunohistochemical/molecular exploratory study. Journal of Pediatric Surgery 2023; 58(3): 587 doi: 10.1016/j.jpedsurg.2022.08.020
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| 12 |
Shuiqing Chi, Peipei Xu, Pu Yu, Guoqing Cao, Haibin Wang, Yongqin Ye, Shuai Li, Yun Zhou, Xiangyang Li, Ying Zhou, Xi Zhang, Huizhong Niu, Lei Xu, Pengcheng Cai, Shaotao Tang. Dynamic analysis of serum MMP-7 and its relationship with disease progression in biliary atresia: a multicenter prospective study. Hepatology International 2022; 16(4): 954 doi: 10.1007/s12072-022-10322-x
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| 13 |
Kaizhi Zhang, Yan Tang, Rui Liu, Zebing Zheng, Chengyan Tang, Yuanmei Liu, Zhu Jin. Intraoperative hepatic subcapsular spider-like telangiectasia sign for the definitive diagnosis of biliary atresia. BMC Pediatrics 2023; 23(1) doi: 10.1186/s12887-022-03831-z
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