Annekathrin Rodiger
Jena, TH, Germany
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 42 publications
Innate immune signaling as a potential pathomechanistic biomarker for distinct subtypes in amyotrophic lateral sclerosis.
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: June 15, 2026
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
Between guidelines and reality: expert neurologists' perspectives on structural resources for ALS care in Germany.
Journal: Neurological research and practice
Published: December 09, 2025
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
Novel COL4A1 missense variant in a case of juvenile stroke.
Journal: Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association
Published: July 22, 2025
Hyperactivity of the non-canonical inflammasome in SPG11 and SPG48.
Journal: EBioMedicine
Published: July 05, 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
Respiratory function in 192 adult patients with spinal muscular atrophy (SMA) treated with nusinersen - a multicenter observational study.
Journal: Orphanet journal of rare diseases
Published: February 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
RIG-I Mediated Neuron-Specific IFN Type 1 Signaling in FUS-ALS Induces Neurodegeneration and Offers New Biomarker-Driven Individualized Treatment Options for (FUS-)ALS.
Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)
Published: December 18, 2024
Last Updated: 09/26/2026