Gilbert Wunderlich

7PUBLICATIONS
80CO-AUTHORS
Gene mappingCell and nuclear divisionMechanobiologyNeurology and neuromuscular diseases
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Publications (7)

|Feb 14, 2026
Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia.

Benita Menden, Rana D Incebacak Eltemur, German Demidov

|Dec 20, 2024
Updated Structure of CNBP Repeat Expansions in Patients With Myotonic Dystrophy Type 2 and Its Implication for Standard Diagnostics.

Martin Wendlandt, Hannes Erdmann, Simone Rost

|Aug 13, 2024
Tissue Doppler ultrasound of arm muscles to assess myotonia in myotonic dystrophies: An exploratory study.

Martin K R Svačina, Alina Sprenger-Svačina, Felix Kohle

|Mar 30, 2024
Genetic forms of tauopathies: inherited causes and implications of Alzheimer's disease-like TAU pathology in primary and secondary tauopathies.

Felix Langerscheidt, Tamara Wied, Mohamed Aghyad Al Kabbani

|Mar 11, 2023
Subclinical motor involvement in nonsystemic vasculitic neuropathy determined by the motor unit number estimation method MScanFit.

Christian Schneider, Meike K Wassermann, Martin K R Svačina

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Frequent Collaborators

1 joint publications

Christian Schneider

1 joint publications

Felix Langerscheidt

1 joint publications

Tamara Wied

1 joint publications

Mohamed Aghyad Al Kabbani