Publications by authors named "Eva Hebert"

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Novel GCH1 Compound Heterozygosity Mutation in Infancy-Onset Generalized Dystonia.
Marina Flotats-Bastardas, Eva Hebert, Miquel Raspall-Chaure, Francina Munell, Alfons Macaya

Neuropediatrics· August 2018

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The expression of the MSC-marker CD73 and of NF2/Merlin are correlated in meningiomas.
Elmar Kirches, Tabea Steffen, Natalie Waldt, Eva Hebert, Doreen Pachow

J Neurooncol· June 2018

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Functional Characterization of Rare RAB12 Variants and Their Role in Musician's and Other Dystonias.
Eva Hebert, Friederike Borngräber, Alexander Schmidt, Aleksandar Rakovic, Ingrid Brænne

Genes (Basel)· October 2017

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In-depth Characterization of the Homodimerization Domain of the Transcription Factor THAP1 and Dystonia-Causing Mutations Therein.
Alev Richter, Ronja Hollstein, Eva Hebert, Franca Vulinovic, Juliane Eckhold

J Mol Neurosci· May 2017

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Novel GNB1 mutations disrupt assembly and function of G protein heterotrimers and cause global developmental delay in humans.
Katja Lohmann, Ikuo Masuho, Dipak N Patil, Hauke Baumann, Eva Hebert

Hum Mol Genet· March 2017

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