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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 20, 2022
Cognitive profiles in pediatric unilobar vs. multilobar epilepsyFrederik Jan Moorhouse, Sonia Cornell, Lucia Gerstl, et al.
Seizure|August 27, 2025
ADAM23 haploinsufficiency as a putative oligogenic contributor in an individual with focal epilepsyMartin Krenn, Karl-Heinz Nenning, Susanne Aull-Watschinger, et al.
Scientific Reports|June 26, 2021
Recanalization strategies in childhood stroke in GermanyMartin Olivieri, Anna-Lisa Sorg, Raphael Weinberger, et al.
Brain : a Journal of Neurology|September 30, 2021
Blood DNA methylation provides an accurate biomarker of KMT2B-related dystonia and predicts onsetNazanin Mirza-Schreiber, Michael Zech, Rory Wilson, et al.
Journal of Neurology|August 25, 2019
Arterial ischemic stroke in infants, children, and adolescents: results of a Germany-wide surveillance study 2015-2017Lucia Gerstl, Raphael Weinberger, Florian Heinen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 3, 2009
Muscle biopsy substantiates long-term MRI alterations one year after a single dose of botulinum toxin injected into the lateral gastrocnemius muscle of healthy volunteersA Sebastian Schroeder, Birgit Ertl-Wagner, Stefanie Britsch, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 27, 2018
Risk factors in childhood arterial ischaemic stroke: Findings from a population-based study in GermanyLucia Gerstl, Raphael Weinberger, Ruediger von Kries, et al.
Gene|November 9, 2020
Locus heterogeneity in two siblings presenting with developmental delay, intellectual disability and autism spectrum disorderMelanie Brugger, Theresa Brunet, Matias Wagner, et al.
Annals of Clinical and Translational Neurology|May 27, 2026
Prominent Movement Disorders in RNU2-2-Related SpliceosomopathyMagdalena Krygier, Ugo Sorrentino, Matias Wagner, et al.
Neuropediatrics|September 11, 2018
A De Novo Missense Variant in POU3F2 Identified in a Child with Global Developmental DelayDominik Sebastian Westphal, Korbinian Maria Riedhammer, Reka Kovacs-Nagy, et al.
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