M Linder-Lucht

Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study

Stefan Groeneweg, Ferdy S. van Geest, Ayhan Abacı et al. · The Lancet Diabetes & Endocrinology · 2020 · 107 citations

Disease Characteristics, Disease Mechanism, Genetic Disorder +10

Cortical Neuromodulation by Constraint-Induced Movement Therapy in Congenital Hemiparesis: An fMRI Study

Hendrik Juenger, M Linder-Lucht, Michael Walther et al. · Neuropediatrics · 2007 · 80 citations

Congenital Hemiparesis, Neurological Disorder, Neuromodulation Therapies +21

Validation of the Gross Motor Function Measure for Use in Children and Adolescents With Traumatic Brain Injuries

M Linder-Lucht, Verena Othmer, Michael Walther et al. · PEDIATRICS · 2007 · 74 citations

Effectiveness of antiepileptic therapy in patients with PCDH19 mutations

J Lotte, Thomas Bast, Peter Borusiak et al. · Seizure · 2016 · 74 citations · Full text

Mendelian Disorder, Genetic Disorder, Antiepileptic Therapy +4

Microdeletion 5q14.3 and anomalies of brain development

Alrun Hotz, Yorck Hellenbroich, Jürgen Sperner et al. · American Journal of Medical Genetics Part A · 2013 · 50 citations