Christoph Munch
Berlin, BE, Germany
Last Updated: 09/26/2026
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Found 29 publications
Minimum important slowing of disease progression as determined by the ALS functional rating scale - a survey of patient expectations toward disease-modifying drugs in ALS.
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: January 20, 2026
Dextromethorphan/quinidine (DMQ) for reducing bulbar symptoms in amyotrophic lateral sclerosis - assessment of treatment experience in a multicenter study.
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: September 11, 2025
Motor phenotypes and neurofilament light chain in genetic amyotrophic lateral sclerosis-results from a multicenter screening program.
Journal: Journal of neurology
Published: September 03, 2025
Agreement Between the Harmonized and the Self-Explanatory Versions of the Revised ALS Functional Rating Scale in a Clinical Setting.
Journal: Muscle & nerve
Published: July 22, 2025
Response to Fortin-Bédard et al. "User expectations and experiences of an assistive robotic arm in amyotrophic lateral sclerosis: a multicenter observational study".
Journal: Neurological research and practice
Published: June 23, 2025
Self-assessment of amyotrophic lateral sclerosis functional rating scale on the patient's smartphone proves to be non-inferior to clinic data capture.
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: February 22, 2025
Motor phenotypes of amyotrophic lateral sclerosis - a three-determinant anatomical classification based on the region of onset, propagation of motor symptoms, and the degree of upper and lower motor neuron dysfunction.
Journal: Neurological research and practice
Published: January 21, 2025
Shared prognostic information in amyotrophic lateral sclerosis - systematic assessment of the patients' perception of neurofilament light chain and the ALS functional rating scale.
Journal: Neurological research and practice
Published: October 19, 2024
SOD1 gene screening in ALS - frequency of mutations, patients' attitudes to genetic information and transition to tofersen treatment in a multi-center program.
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: September 13, 2024
Provision, cough efficacy and treatment satisfaction of mechanical insufflation-exsufflation in a large multicenter cohort of patients with amyotrophic lateral sclerosis.
Journal: Scientific reports
Published: May 31, 2024
User expectations and experiences of an assistive robotic arm in amyotrophic lateral sclerosis: a multicenter observational study.
Journal: Neurological research and practice
Published: April 14, 2024
Serum neurofilament light chain in distinct phenotypes of amyotrophic lateral sclerosis: A longitudinal, multicenter study.
Journal: European journal of neurology
Published: February 25, 2024
Last Updated: 09/26/2026