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William F. Balistreri
Researcher at University of Cincinnati Academic Health Center
Publications - 99
Citations - 4122
William F. Balistreri is an academic researcher from University of Cincinnati Academic Health Center. The author has contributed to research in topics: Liver disease & Liver transplantation. The author has an hindex of 34, co-authored 99 publications receiving 3982 citations. Previous affiliations of William F. Balistreri include Hospital Research Foundation & Foundation Center.
Papers
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Journal ArticleDOI
High‐fructose, medium chain trans fat diet induces liver fibrosis and elevates plasma coenzyme Q9 in a novel murine model of obesity and nonalcoholic steatohepatitis
Rohit Kohli,Michelle Kirby,Stavra A. Xanthakos,Samir Softic,Ariel E. Feldstein,Vijay Saxena,Peter H. Tang,Lili Miles,Michael V. Miles,William F. Balistreri,Stephen C. Woods,Randy J. Seeley +11 more
TL;DR: It is demonstrated that nongenetically modified mice maintained on an HFHC diet in addition to developing obesity have increased hepatic ROS and a NASH‐like phenotype with significant fibrosis.
Journal ArticleDOI
Biliary atresia: Current concepts and research directions. Summary of a symposium
William F. Balistreri,Richard J. Grand,J H Hoofnagle,Frederick J. Suchy,Frederick C. Ryckman,David H. Perlmutter,Ronald J. Sokol +6 more
TL;DR: An increased awareness to ensure early diagnosis and development of methods to prevent progressive fibrosis are needed are needed, and considerations are dependent on detailed studies of the pathogenesis of BA.
Book
Liver Disease in Children
TL;DR: Part 1 Pathophysiology of paediatric liver disease: structural and functional development of the liver mechanisms and morphology of cholestasis the cholangiopathies fulminant hepatic failure in children portal hypertension and other conditions and issues in paediatric hepatology.
Journal ArticleDOI
Biliary Atresia and Reovirus Type 3 Infection
TL;DR: Interest in reovirus type 3 (reo-3) as a potential cause of biliary atresia was stimulated by the observations of Stanley et al.
Journal ArticleDOI
Physiologic cholestasis: Elevation of the primary serum bile acid concentrations in normal infants
Frederick J. Suchy,Frederick J. Suchy,William F. Balistreri,William F. Balistreri,James E. Heubi,James E. Heubi,John E. Searcy,John E. Searcy,Ron S. Levin,Ron S. Levin +9 more
TL;DR: Serum concentrations of the primary bile acids in normal infants were determined to define age-related changes and there was a striking rise in serum cholylglycine and conjugates of chenodeoxycholate during the first few days of life over levels detected in cord sera.