Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis
Michèl A.A.P. Willemsen(Radboud University Nijmegen), Ron A. Wevers(Radboud University Nijmegen), Jan Smeıtınk(Khondrion (Netherlands)), Monique M. Ryan(Royal Children's Hospital), Alec Aeby(Université Libre de Bruxelles), Nenad Blau(University Children's Hospital Zurich), André Mégarbané(University Medical Center Groningen), Maria Alice Donati(University of Florence), Alessandro P. Burlina(Santa Maria Nuova Hospital), Vincenzo Leuzzi(Sapienza University of Rome), Frits A. Wijburg(Emma Kinderziekenhuis), J. B. de Klerk(Erasmus MC - Sophia Children’s Hospital), Jürgen Seeger(Deutsche Klinik für Diagnostik), Dimitrios Zafeiriou(Aristotle University of Thessaloniki), Fernando Kok(Universidade de São Paulo), Marjo S. van der Knaap(Amsterdam Neuroscience), W.O. Renier(Canisius-Wilhelmina Ziekenhuis), Pierre Rondot(Bicêtre Hospital), Maximilian Haeussler(University of California, Santa Cruz), J.F. de Rijk-van Andel(Amphia Ziekenhuis), Bridget Wilcken(Children's Hospital at Westmead), Bernhard Weschke(Charité - Universitätsmedizin Berlin), Hae Hyuk Jung(University Hospital of Zurich), Pascale de Lonlay(Université Paris Cité), Padraic J. Grattan‐Smith(Sydney Children's Hospital), Erik‐Jan Kamsteeg(Radboud University Nijmegen), Evangeline Wassmer(Birmingham Children's Hospital), Gerry C. H. Steenbergen‐Spanjers(Radboud University Nijmegen), B. Geurtz(Radboud University Nijmegen), G. F. Hoffmann(Heidelberg University), H. Monaghan(Children's Health Ireland at Crumlin), Marcel M. Verbeek(Radboud University Nijmegen)
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