Author

Wolfgang Brück

Universitätsmedizin GöttingenORCID 0000-0002-6881-4479Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 3

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Assay:imaging· 2 Research Focus:spatial domain detection· 1

Frequent Co-Authors

Christine StadelmanniD· 3 shared Cristina GranzieraiD· 2 shared Erik BahniD· 2 shared Ludwig KapposiD· 2 shared Matthias WeigeliD· 2 shared Peter DechentiD· 2 shared Po‐Jui LuiD· 2 shared Riccardo GalbuseraiD· 2 shared

Activity by Year

2019-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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3 shared papersNeuroscience

Christine StadelmannORCID

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3 papers

Recent·Most cited

NeurosciencebioRxivPreprintApr 18, 2024

Cerebellar Ex Vivo Magnetic Resonance Imaging at its Feasibility Limit: Up to 77-Microns Isotropic Resolution using Low-Bandwidth Balanced Steady State Free Precession (LoBa-bSSFP) Sequences and 3T Standard Equipment

Matthias Weigel, Peter Dechent, Riccardo Galbusera…·Cristina Granziera

This paper demonstrates a new MRI technique, LoBa-bSSFP, achieving 77-micron isotropic resolution for ex vivo cerebellar imaging using standard 3T equipment.

DOI 10.1101/2024.04.18.589707

imagingexperimental assay

𝕏 PostBluesky

NeuroscienceScientific ReportsPeer-reviewedJul 29, 2021

Imaging Multiple Sclerosis Pathology at 160μm Isotropic Resolution by Human Whole-Brain Ex Vivo Magnetic Resonance Imaging at 3T

Matthias Weigel, Peter Dechent, Riccardo Galbusera…·Cristina Granziera

This paper develops a 3T MRI method for high-resolution human whole-brain imaging and applies it to study multiple sclerosis pathology.

10 citations

𝕏 PostBluesky

NeuroscienceExperimental NeurologyPeer-reviewedMay 24, 2019

Homozygous NMNAT2 mutation in sisters with polyneuropathy and erythromelalgia

Peter Huppke, Eike Wegener, Jonathan Gilley…·Michael P. Coleman

The paper identifies a homozygous NMNAT2 mutation causing polyneuropathy and erythromelalgia in two sisters, linking it to axon degeneration and supporting the role of the Wallerian pathway in human disease.

67 citationstop 3%

𝕏 PostBluesky