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Fighting Neurodegeneration: Targeting our Fight or Flight Response as a Therapeutic Model for Amyotrophic Lateral Sclerosis - Nikki Boon

Emory University
2026
ALS
amyotrophic lateral sclerosis
neurodegeneration
Sympathetic Nervous System
Fight or Flight Response
Motor Neurons
Muscle Biology
Neuromuscular Disease
neuroscience
neurobiology
Muscle Degeneration
biomarkers
early diagnosis
disease progression
neuroprotection
Immunofluorescence
Immunohistochemistry
Protein Assays
HPLC
Gene Transcription
receptors
cell signalling
Muscle Physiology
mitochondria
neurodegenerative disease
translational medicine
biomedical research
clinical neuroscience
therapeutic targets
precision medicine
nervous system
Muscle Health
neurophysiology
molecular biology
cell biology
Neuroimmune Interactions
ALS Research
biomedical science
neurology
disease mechanisms

This research shows that the sympathetic nervous system is disrupted at the earliest stages of ALS, despite sympathetic neurons themselves remaining intact. Early loss of signalling receptors may contribute to muscle degeneration and disease progression, identifying new opportunities for earlier diagnosis and therapies that preserve muscle function and improve patient outcomes.

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