Ferenci, Peter; Stremmel, Wolfgang; Członkowska, Anna; Szalay, Ferenc; Viveiros, Andre; Stättermayer, Albert Friedrich; Bruha, Radan; Houwen, Roderick; Pop, Tudor; Stauber, Rudolf; Gschwantler, Michael; Pfeiffenberger, Jan; Yurdaydin, Cihan; Aigner, Elmar; Steindl-Munda, Petra; Dienes, Hans-Peter; Zoller, Heinz; Weiss, Karl Heinz
(John Wiley & Sons Inc., 2019-04)
Wilson disease (WD) is an inherited disorder of hepatic copper metabolism with considerable variation in clinical presentations, the most common ones being liver disease and neuropsychiatric disturbances. This study ...