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Autor:
Hana Ayoob, Judith McCaffrey, Andrea Zatkova, Christa van Kan, Carin Junestrand, Jonathan C. Jarvis, Andrew T. Hughes, Kim-Hanh Le Quan Sang, Helen Bygott, Gordon A. Ross, Lakshminarayan R. Ranganath, Richard Imrich, Anthony K Hall, Dinny Laan, Trevor Cox, Peter Christensen, Mattias Rudebeck, James A. Gallagher, Nicolas Sireau, Torbjörn Kullenberg, Lennart Svensson, Eftychia E. Psarelli, Birgitta Olsson, Daniela Braconi, Federica Genovese, Richard Fitzgerald, Oliver Timmis, Jozef Rovensky, Martina Nemethova, Anna M. Milan, Arvid Cronlund, Annalisa Santucci, Johan Szamosi, John Dutton, M. C. Briggs
Publikováno v:
Annals of the rheumatic diseases. 75(2)
Background Alkaptonuria (AKU) is a serious genetic disease characterised by premature spondyloarthropathy. Homogentisate-lowering therapy is being investigated for AKU. Nitisinone decreases homogentisic acid (HGA) in AKU but the dose-response relatio