Friedrich Erdlenbruch

4PUBLICATIONS
46CO-AUTHORS
Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Gene mapping
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Publications (4)

|Dec 26, 2025
Cerebellar ataxias and functional movement disorders: navigating clinical overlap.

Friedrich Erdlenbruch, Andreas Thieme, Christel Depienne

|Feb 20, 2025
Progression of biological markers in spinocerebellar ataxia type 3: analysis of longitudinal data from the ESMI cohort.

Moritz Berger, Hector Garcia-Moreno, Monica Ferreira

|Sep 03, 2024
Identification and characterisation of pathogenic and non-pathogenic FGF14 repeat expansions.

Lars Mohren, Friedrich Erdlenbruch, Elsa Leitão

|Apr 29, 2024
A GGC-repeat expansion in ZFHX3 encoding polyglycine causes spinocerebellar ataxia type 4 and impairs autophagy.

Karla P Figueroa, Caspar Gross, Elena Buena-Atienza

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