Risk of HBV reactivation during therapies for HCC: A systematic review
Margarita Papatheodoridi, Maria Tampaki, Anna S. Lok, George V. Papatheodoridis – 12 November 2021
Margarita Papatheodoridi, Maria Tampaki, Anna S. Lok, George V. Papatheodoridis – 12 November 2021
Thomas Damgaard Sandahl, Lars C. Gormsen, Kristoffer Kjærgaard, Mikkel Holm Vendelbo, Ditte Emilie Munk, Ole Lajord Munk, Dirk Bender, Susanne Keiding, Karina H. Vase, Kim Frisch, Hendrik Vilstrup, Peter Ott – 12 November 2021
Ezhilarasan Devaraj, Elumalai Perumal, Raghunandhakumar Subramaniyan, Najimi Mustapha – 12 November 2021
Julieta Politi, Juan‐Miguel Guerras, Marta Donat, María J. Belza, Elena Ronda, Gregorio Barrio, Enrique Regidor – 11 November 2021
Yana Davidov, Keren Tsaraf, Oranit Cohen‐Ezra, Mariya Likhter, Gil Ben Yakov, Itzchak Levy, Einav G. Levin, Yaniv Lustig, Orna Mor, Galia Rahav, Ziv Ben Ari – 11 November 2021 – The BNT162b2 messenger RNA (mRNA) vaccine against severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) has been shown to be safe and effective in immunocompetent patients. The safety and efficacy of this vaccine in liver transplantation (LT) recipients is still under evaluation. The objective of this study was to assess the safety and efficacy of the BNT162b2 vaccine among transplant recipients.
Juan Yang, Jianming Ye, Tengfei Ma, Fangfang Tang, Li Huang, Zhen Liu, Song Tian, Xu Cheng, Li Zhang, Zhenli Guo, Fuping Tu, Miao He, Xueming Xu, Xiaojuan Lu, Yanyang Wu, Xiaoli Zeng, Jiahua Zou, Xiangcai Wang, Weijie Peng, Peng Zhang – 11 November 2021
Eun Ran Kim, Jeong Su Park, Jin Hee Kim, Ji Young Oh, In Jeong Oh, Da Hyun Choi, Yu seol Lee, I. Seul Park, SeungWon Kim, Da Hyun Lee, Jae Hee Cheon, Jin‐Woo Bae, Minyoung Lee, Jin Won Cho, In Bok An, Eun Joo Nam, Sang‐In Yang, Myung‐Shik Lee, Soo Han Bae, Yong‐ho Lee – 11 November 2021
Lu Tian, Luqing Zhao, Karen Man‐Fong Sze, Charles Shing Kam, Vanessa Sheung‐In Ming, Xia Wang, Vanilla Xin Zhang, Daniel Wai‐Hung Ho, Tan‐To Cheung, Lo‐Kong Chan, Irene Oi‐Lin Ng – 11 November 2021
Complex multi-directional interactions occur between the gut microbiota and the liver. A disturbance of this delicate homeostasis can contribute to liver disease. Effects of untargeted microbiota therapies including antibiotics, probiotics and fecal microbiota transplantation, have been assessed in clinical trials. Precision and targeted modifications such as engineered bacteria, postbiotics and phages, can precisely edit the microbiota and modify liver disease progression.
This program combines didactic lectures and lively debate to examine controversies in the screening and prevention of clinically significant portal hypertension. Talks cover groundbreaking advances in basic, translational, outcomes, and clinical research in portal hypertension that may be incorporated into clinical practice, along with new pharmacologic interventions to prevent disease progression in these patients.