Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Jin-fa Tou"'
Autor:
Si-Si Yang, Wen-Chang Huang, Peng Wang, Fang-Qi Gong, Tai-Xiang Liu, Jin-Fa Tou, Deng-Ming Lai
Publikováno v:
BMC Pediatrics, Vol 23, Iss 1, Pp 1-6 (2023)
Abstract Purpose The purpose of this study was to explore echocardiographic parameters of the left ventricle (LV) in relation to the outcomes of omphalocele neonates with pulmonary hypertension (PH). Methods This retrospective study was conducted amo
Externí odkaz:
https://doaj.org/article/f4e10dc9d47b4a2095f9a28b1c8a8c79
Publikováno v:
World Journal of Clinical Cases
Background Blue rubber bleb naevus syndrome (BRBNS) is a rare disease that usually presents with multiple venous malformations in the skin and gastrointestinal tract. Lesions located in the gastrointestinal tract always result in chronic gastrointest
Autor:
Bin Wang, Wei Gao, Hongqiang Bian, Zhi-Jun Zhu, Chen Yu, Jiexiong Feng, Le Li, Qingyun Gou, Weibing Tang, Hongxia Ren, Jianghua Zhan, Yurui Wu, Yingchao Li, Yang Chen, Jinfu Jia, Jin-fa Tou
Publikováno v:
Pediatric Surgery International. 36:711-718
We evaluated the demographic of biliary atresia (BA) children from twins family and aimed to investigated what it can add to the twins’ literature and our understanding of the disease. This study contains 11 medical centers in mainland China and th
Autor:
Xiang Zou, Jun Lu, Xiao-Jun Yuan, Jin-Fa Tou, Yong-Jun Fang, Ci Pan, Huan-Min Wang, Xiang Liu, Hui Jiang, Ye-Ming Wu, Meng-Jie Tang, Yang Li, Zhang-Lin Li, Keren Zhang, Wei-Song Li
Publikováno v:
Cancer Letters. 375:39-46
The purpose of this study is to report the first nationwide protocol (Wuhan Protocol) developed by Chinese Children's Cancer Group and the results of multidisciplinary effort in treating hepatoblastoma. In this study, we reported the final analysis,
Autor:
Li-Feng Zhang1 zhanglifeng1999@163.com, Jin-Fa Tou1 toujingfa@gmail.com, Xiang Wang1 wangxiang81@gmail.com, Wei-Zhong Gu2 zjuchild@163.com, Xiao-Hui Ma3, Qi Qin1 qinqi771@163.com
Publikováno v:
World Journal of Surgical Oncology. 2014, Vol. 12 Issue 1, p1-10. 10p.
Autor:
Bin Yi, Edwin Kin Wai Chan, Emily H. M. Wong, Pak C. Sham, Xuelai Liu, Juncheng Liu, Liu-ming Huang, Vincent Chi Hang Lui, Stacey S. Cherny, G Cheng, Long Cui, Xuan-Zhao Wu, Man-Ting So, William Wai-Chun Cheng, Paul F. O′Reilly, Kenny Ye, Clara S. Tang, Jiakang Yu, Ivy Hau-Yee Chan, Maria-Mercè Garcia-Barceló, Kenneth K. Y. Wong, Xiao Dong, Ruizhong Zhang, Patrick Ho Yu Chung, Wei Zhong, Hongxia Ren, Paul K.H. Tam, Jin-fa Tou, Elly Sau-Wai Ngan, Xiu Qiu, Bin Wang, Huimin Xia, Xiaoping Miao
Publikováno v:
Journal of Hepatology. 59:1285-1291
Background & Aims Biliary atresia (BA) is a rare and most severe cholestatic disease in neonates, but the pathogenic mechanisms are unknown. Through a previous genome wide association study (GWAS) on Han Chinese, we discovered association of the 10q2
Autor:
Zhixin Li, Hualong Wang, Paul Kwang-Hang Tam, Peng Li, Hong Liu, Xuehan Zhuang, Zhen-wei Yuan, Bin Yi, Michelle Yu, Maria-Mercè Garcia-Barceló, Xuelai Liu, Pak C. Sham, Elly Sau-Wai Ngan, Frank Pui-Ling Lai, Clara S. Tang, Kevin Y. Yip, Xi Zhang, Kathryn S. E. Cheah, Ngoc Diem Ngo, Qiji Liu, Furen Zhang, Sin-Ting Lau, Xiao-bing Sun, Xiaoping Miao, Shao-tao Tang, Ruizhong Zhang, Alexander Xi Fu, Liu-ming Huang, Kathy Nga-Chu Lui, Wanling Yang, Man-Ting So, Jin-fa Tou, Xiao Dong
Publikováno v:
Gastroenterology. 155:1908-1922.e5
Background & Aims Hirschsprung disease, or congenital aganglionosis, is believed to be oligogenic—that is, caused by multiple genetic factors. We performed whole-genome sequence analyses of patients with Hirschsprung disease to identify genetic fac
Autor:
Maria-Mercè, Garcia-Barceló, Ming-Yiu, Yeung, Xiao-Ping, Miao, Clara Sze-Man, Tang, Guo, Cheng, Guo, Chen, Man-Ting, So, Elly Sau-Wai, Ngan, Vincent Chi-Hang, Lui, Yan, Chen, Xue-Lai, Liu, Kenneth-Jeremy W S, Hui, Long, Li, Wei-Hong, Guo, Xiao-Bin, Sun, Jin-Fa, Tou, Kin-Wai, Chan, Xuan-Zhao, Wu, You-Qiang, Song, Danny, Chan, Kenneth, Cheung, Patrick Ho-Yu, Chung, Kenneth Kak-Yuen, Wong, Pak-Chung, Sham, Stacey S, Cherny, Paul Kwong-Hang, Tam
Publikováno v:
Human Molecular Genetics. 19:2917-2925
Biliary atresia (BA) is characterized by the progressive fibrosclerosing obliteration of the extrahepatic biliary system during the first few weeks of life. Despite early diagnosis and prompt surgical intervention, the disease progresses to cirrhosis
Autor:
Xiaoli Shu, Ling-Rong Yang, Haifang Cai, Jin-Fa Tou, Xi Yang, Zheng Shen, Ting Zhang, Weizhong Gu, Mizu Jiang
Publikováno v:
World Journal of Surgical Oncology, Vol 10, Iss 1, p 219 (2012)
World Journal of Surgical Oncology
World Journal of Surgical Oncology
Background Dysfunction of the 5-hydroxytryptamine (5-HT) signaling pathway can lead to gastrointestinal motility and secretion abnormalities and to visceral hypersensitivity. The aim of this study is to investigate the role of 5-HT in reflux-induced
Autor:
Stacey S. Cherny, Elly Sau-Wai Ngan, Feng-Qin Liu, Cathy K.Y. Shum, Wei-hong Guo, Ming-Yiu Yeung, Kenneth K. Y. Wong, You-Qiang Song, Zhen-wei Yuan, Paul K.H. Tam, Kenneth M.C. Cheung, Xiaoping Miao, Yan Chen, Lei Liu, Pak C. Sham, Jin-fa Tou, Man-Ting So, Vincent Chi Hang Lui, Thomas Y.Y. Leon, Clara S. Tang, Xiao-bing Sun, Maria-Mercè Garcia-Barceló, Liu-ming Huang, Daniel W. Chan
Hirschsprung's disease (HSCR), or aganglionic megacolon, is a congenital disorder characterized by the absence of enteric ganglia in variable portions of the distal intestine. RET is a well-established susceptibility locus, although existing evidence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23fccdbc5f5350dc392d4b807adde4b8
http://hdl.handle.net/10722/92121
http://hdl.handle.net/10722/92121