Patients with Allan‐Herndon‐Dudley Syndrome (<scp>MCT8</scp> Deficiency) Display Symptoms of Parkinsonism in Childhood and Respond to Levodopa/Carbidopa Treatment
Nina‐Maria Wilpert(Humboldt-Universität zu Berlin), Markus Schuelke(Humboldt-Universität zu Berlin), Roser Pons(National and Kapodistrian University of Athens), Andrea Dell’Orco(Charité - Universitätsmedizin Berlin), M. Bauer(Max Planck Institute for Plasma Physics), Thomas Opladen(Heidelberg University), Christiane Grolik(Kliniken der Stadt Köln), Angela Hewitt(University of Rochester Medicine), Knut Brockmann(Universitätsmedizin Göttingen), Catharina Lange(Humboldt-Universität zu Berlin), Annika Zink(Düsseldorf University Hospital), Angela M. Kaindl(German Centre for Cardiovascular Research), Heiko Krude(Humboldt-Universität zu Berlin), Christian Furth(Humboldt-Universität zu Berlin), Sabine Jung‐Klawitter(Paul Ehrlich Institut), Christina Reinauer(Düsseldorf University Hospital), Anna Tietze(Humboldt-Universität zu Berlin), Monika Wahle(Humboldt-Universität zu Berlin), Stine Christ(Heidelberg University), Alessandro Prigione(Düsseldorf University Hospital), Stephan Menz(Bayer (Germany)), Marie‐Thérèse Henke(Humboldt-Universität zu Berlin)
Cited by 4
Related Papers
Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans
|Nature Genetics|1998|1.7k
Brain energy rescue: an emerging therapeutic concept for neurodegenerative disorders of ageing
|Nature Reviews Drug Discovery|2020|982
Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation
|The Lancet|2004|707
The Senescence-Related Mitochondrial/Oxidative Stress Pathway is Repressed in Human Induced Pluripotent Stem Cells
|Stem Cells|2010|607
European Society for Paediatric Endocrinology Consensus Guidelines on Screening, Diagnosis, and Management of Congenital Hypothyroidism
|The Journal of Clinical Endocrinology & Metabolism|2014|569