Author

E. Mercuri

3 papers indexed here

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Open access Sep 2026

Circulating extracellular vesicle lipidomics identifies distinct signatures of amyotrophic lateral sclerosis and spinal muscular atrophy

Amyotrophic lateral sclerosis (ALS) is a heterogeneous neurodegenerative disorder lacking established biomarkers of underlying disease biology. Here, we identify lipidomic signatures of circulating extracellular vesicles (EVs) that distinguish ALS from neurologically healthy controls and related neuromuscular diseases....

V. Ricotti, A. Fogel, M. van den Bosch et al. · medRxiv · 0 citations

Review Open access Sep 2026

Adrenal insufficiency in individuals with Duchenne muscular dystrophy treated with glucocorticoids: Insights from the past, current challenges, and future directions

Duchenne muscular dystrophy (DMD) is an X-linked recessive dystrophinopathy characterized by progressive loss of muscle strength, respiratory insufficiency, cardiac dysfunction, and premature death. Despite a rapidly evolving therapeutic landscape that now includes multiple disease modifying treatments including exon s...

D. Weber, Alexandra Ahmet, K. Kinnett et al. · Journal of Neuromuscular Dis... · 0 citations

Open access Jul 2026

Emotional and Behavioral Profiles in Neurodevelopmental and Neuromuscular Disorders: A Comparative Study Using the Child Behavior Checklist

Children with ADHD showed the highest overall emotional–behavioral burden, whereas ASD and SLD were characterized by greater internalizing difficulties and DMD by a distinct emotional–behavioral profile, using the same standardized CBCL/6–18 assessment.

D. P. Chieffo, Federica Moriconi, Valentina Delle Donne et al. · Children · 0 citations