Christoph Kamm

8PUBLICATIONS
67CO-AUTHORS
NeurogeneticsGene expression (incl. microarray and other genome-wide approaches)Gene mappingCell and nuclear divisionNeurology and neuromuscular diseases
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Publications (8)

|Sep 12, 2025
Phenotypic intrafamilial variability of 5q-associated spinal muscular atrophy: A systematic multicentre sibling study.

Benedikt Becker, Isabell Cordts, Jutta Becker

|Sep 17, 2024
Genetic Risk Factors in Isolated Dystonia Escape Genome-Wide Association Studies.

Björn-Hergen Laabs, Katja Lohmann, Eva-Juliane Vollstedt

|Jan 12, 2024
Large-Scale Screening: Phenotypic and Mutational Spectrum in Isolated and Combined Dystonia Genes.

Mirja Thomsen, Katrin Marth, Sebastian Loens

|Apr 07, 2023
Autosomal Recessive Cerebellar Ataxias in Europe: Frequency, Onset, and Severity in 677 Patients.

Andreas Traschütz, Astrid D Adarmes-Gomez, Mathieu Anheim

|Jan 25, 2023
Evolution of Clinical Outcome Measures and Biomarkers in Sporadic Adult-Onset Degenerative Ataxia.

Demet Oender, Jennifer Faber, Carlo Wilke

|Apr 26, 2020
Frequency and risk factors of antibody-induced secondary failure of botulinum neurotoxin therapy.

Uwe Walter, Christopher Mühlenhoff, Reiner Benecke

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