Inclusion And Diversity Committee
The Inclusion and Diversity Committee will approve and recommend efforts to promote involvement and expand access to leadership opportunities across diverse populations of the AASLD membership.
The Inclusion and Diversity Committee will approve and recommend efforts to promote involvement and expand access to leadership opportunities across diverse populations of the AASLD membership.
The Individual Fundraising Committee supports and supplements the fundraising efforts of the AASLD Foundation.
The Industry Advancement Committee coordinates corporate fundraising activities.
The Journals Publications committee defines, manages, and oversees the publication activities of AASLD and to provide quality publications based on member needs.
Use of the American Association for the Study of Liver Disease’s ("AASLD") World Wide Web pages (“AASLD website”) is subject to the terms and conditions (“Terms of Use”) set forth below.
Michel A. Struwe, Bernd Clement, Axel Scheidig – 12 May 2022
Kelly L. Hayward, Vikas Bansal, Patricia C. Valery, Katharine M. Irvine, Penny L. Wright, Caroline J. Tallis, Katherine A. Stuart, W. Neil Cottrell, Jennifer H. Martin, Elizabeth E. Powell – 12 May 2022
Jasmohan S. Bajaj, Marcela Peňa Rodriguez, Andrew Fagan, Sara McGeorge, Richard K. Sterling, Hannah Lee, Velimir Luketic, Michael Fuchs, Brian C. Davis, Masoumeh Sikaroodi, Patrick M. Gillevet – 12 May 2022
Nidhi P. Goyal, Sara B. Rosenthal, Chanod Nasamran, Cynthia A. Behling, Jorge E. Angeles, Mark H. Fishbein, Kathryn E. Harlow, Ajay K. Jain, Jean P. Molleston, Kimberly P. Newton, Patricia Ugalde‐Nicalo, Stavra A. Xanthankos, Katherine Yates, Nicholas J. Schork, Kathleen M. Fisch, Jeffrey B. Schwimmer, for the NASH Clinical Research Network – 12 May 2022
Xiaoxiao Wang, Xiaohe Li, Rui Jin, Jia Yang, Rui Huang, Lai Wei, Feng Liu, Huiying Rao – 12 May 2022 – Metabolic‐associated fatty liver disease (MAFLD) is a series of liver diseases based on liver steatosis and metabolic disorders. Steatosis, as the core factor in MAFLD diagnosis, and fibrosis, as the major determinant of adverse outcomes of MAFLD, need to be assessed simply and accurately. In this study, we explored the significance of mid‐upper arm circumference (MUAC) in evaluating liver steatosis and fibrosis in patients with MAFLD.