Rebecca Herzog
8PUBLICATIONS
62CO-AUTHORS
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Publications (8)
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|Jun 24, 2025
Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.Axel Schmidt, Magdalena Danyel, Kathrin Grundmann
|Jul 22, 2024
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.Axel Schmidt, Magdalena Danyel, Kathrin Grundmann
|Aug 26, 2023
Neuronavigated Cerebellar 50 Hz tACS: Attenuation of Stimulation Effects by Motor Sequence Learning.Rebecca Herzog, Christina Bolte, Jan-Ole Radecke
|Feb 12, 2022
De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia.Liedewei Van de Vondel, Jonathan De Winter, Danique Beijer
|Dec 15, 2021
Relationship of Genotype, Phenotype, and Treatment in Dopa-Responsive Dystonia: MDSGene Review.Anne Weissbach, Martje G Pauly, Rebecca Herzog
|Jun 06, 2021
Zonisamide-responsive myoclonus in SEMA6B-associated progressive myoclonic epilepsy.Rebecca Herzog, Yorck Hellenbroich, Norbert Brüggemann
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Frequent Collaborators
5 joint publications
Katja Lohmann
4 joint publications
Martje Pauly
2 joint publications
Norbert Brüggemann
2 joint publications
Alexander Münchau
2 joint publications
Tobias Haack
2 joint publications
Alexej Knaus
2 joint publications
Hannah Klinkhammer
2 joint publications
Hartmut Engels
2 joint publications
Tzung-Chien Hsieh
2 joint publications
Theresa Brunet
