Literature DB >> 16847302

A rare cause of nonalcoholic fatty liver disease.

Sandra Ciesek, Johannes Hadem, Judith Fischer, Michael P Manns, Christian P Strassburg.   

Abstract

Entities:  

Mesh：

Year:  2006        PMID： 16847302     DOI： 10.7326/0003-4819-145-2-200607180-00021

Source DB:  PubMed          Journal:  Ann Intern Med        ISSN： 0003-4819            Impact factor:   25.391


× No keyword cloud information.
  4 in total

Review 1.  CGI-58: Versatile Regulator of Intracellular Lipid Droplet Homeostasis.

Authors:  Liqing Yu; Yi Li; Alison Grisé; Huan Wang
Journal:  Adv Exp Med Biol       Date:  2020       Impact factor: 2.622

2.  Dorfman-Chanarin Syndrome: A Rare Cause of Metabolic Associated Fatty Liver Disease Related to Homozygosity of the Nonsense Mutation c.934C>T (p.R312*).

Authors:  Rita Quelhas da Costa; Francisco Laranjeira; Isaura Duarte Ribeiro; António Filipe Santos; Filipe Nery
Journal:  GE Port J Gastroenterol       Date:  2021-07-07

3.  Deficiency of liver Comparative Gene Identification-58 causes steatohepatitis and fibrosis in mice.

Authors:  Feng Guo; Yinyan Ma; Anil K G Kadegowda; Jenna L Betters; Ping Xie; George Liu; Xiuli Liu; Hongming Miao; Juanjuan Ou; Xiong Su; Zhenlin Zheng; Bingzhong Xue; Hang Shi; Liqing Yu
Journal:  J Lipid Res       Date:  2013-06-03       Impact factor: 5.922

4.  Clinical and genetic characterization of Chanarin-Dorfman syndrome patients: first report of large deletions in the ABHD5 gene.

Authors:  Chiara Redaelli; Rosalind A Coleman; Laura Moro; Catherine Dacou-Voutetakis; Solaf Mohamed Elsayed; Daniele Prati; Agostino Colli; Donatella Mela; Roberto Colombo; Daniela Tavian
Journal:  Orphanet J Rare Dis       Date:  2010-12-01       Impact factor: 4.123
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.