Need for the clarification of data in a recent meta‐analysis about cytokine gene polymorphisms and acute liver graft rejection
Fei Liu, Yonggang Wei, Bo Li, Lvnan Yan – 28 June 2011
It is time to look inward
Robert M. Merion – 28 June 2011
Telaprevir, boceprevir, cytochrome P450 and immunosuppressive agents — A potentially lethal cocktail
Michael Charlton – 26 June 2011
Liver cancer: Still a long way to go
Jordi Bruix – 26 June 2011
A glimpse at the future of hepatitis C therapy: The INFORM trial
Lei Y. Lim, Paul Y. Kwo – 26 June 2011
Copper toxicity in Wilson disease explained in a new way
Uta Merle, Wolfgang Stremmel – 26 June 2011
Anti‐chemokine therapy for the treatment of hepatic fibrosis: An attractive approach
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Grant A. Ramm – 26 June 2011
Model for end‐stage liver disease exceptions in the context of the french model for end‐stage liver disease score–based liver allocation system
Claire Francoz, Jacques Belghiti, Denis Castaing, Olivier Chazouillères, Jean‐Charles Duclos‐Vallée, Christophe Duvoux, Jan Lerut, Yves‐Patrice Le Treut, Richard Moreau, Ameet Mandot, Georges Pageaux, Didier Samuel, Dominique Thabut, Dominique Valla, François Durand – 21 June 2011 – Model for End‐Stage Liver Disease (MELD) score–based allocation systems have been adopted by most countries in Europe and North America. Indeed, the MELD score is a robust marker of early mortality for patients with cirrhosis.
Milan criteria in liver transplantation for hepatocellular carcinoma: An evidence‐based analysis of 15 years of experience
Vincenzo Mazzaferro, Sherrie Bhoori, Carlo Sposito, Marco Bongini, Martin Langer, Rosalba Miceli, Luigi Mariani – 21 June 2011
Optimization of the dosing regimen of mycophenolate mofetil in pediatric liver transplant recipients
Caroline Barau, Aurélie Barrail‐Tran, Bogdan Hemerziu, Dalila Habes, Anne‐Marie Taburet, Dominique Debray, Valérie Furlan – 21 June 2011 – Mycophenolate mofetil (MMF) is now commonly used in pediatric liver transplant recipients, but no clear recommendations about the dosing regimen have been made for this population. The aim of this study was to determine the MMF dosage required for pediatric liver transplant recipients to achieve an area under the plasma concentration–time curve from 0 to 12 hours (AUC0‐12) for mycophenolic acid (MPA) greater than 30 mg hour/L.