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Frontiers in Molecular Neuroscience|May 12, 2020
LAMA2 Neuropathies: Human Findings and Pathomechanisms From Mouse ModelsStefano Carlo Previtali, Alberto Andrea Zambon
The Neuroscientist : a Review Journal Bringing Neurobiology, Neurology and Psychiatry|February 18, 2015
How Schwann Cells Sort Axons: New ConceptsM Laura Feltri, Yannick Poitelon, Stefano Carlo Previtali
Brain Sciences|September 28, 2021
Animal Models as a Tool to Design Therapeutical Strategies for CMT-like Hereditary NeuropathiesLuca Bosco, Yuri Matteo Falzone, Stefano Carlo Previtali
Cellular and Molecular Life Sciences : CMLS|April 28, 2024
Molecular mechanisms and therapeutic strategies for neuromuscular diseasesAlberto Andrea Zambon, Yuri Matteo Falzone, Alessandra Bolino, et al.
Brain : a Journal of Neurology|October 23, 2025
Neuromuscular disorders with evidence of both neuropathic and myopathic phenotypeChristian Laurini, Luca Bosco, Alberto Andrea Zambon, et al.
Neurology. Genetics|March 26, 2026
Expanding the AFG3L2 Spectrum: A Link to Axonal NeuropathyAlessandra Rocco, Christian Laurini, Yuri Matteo Falzone, et al.
Neural Regeneration Research|March 27, 2025
Novel therapies for myasthenia gravis: translational research from animal models to clinical applicationBenedetta Sorrenti, Christian Laurini, Luca Bosco, et al.
Clinical and Experimental Rheumatology|November 19, 2021
Dipeptidyl peptidase 4/CD26 expression in human idiopathic inflammatory myopathies reveals skeletal muscle injury and vascular inflammationRebecca De Lorenzo, Antonella Monno, Clara Sciorati, et al.
European Radiology|June 28, 2015
Muscle MRI findings in facioscapulohumeral muscular dystrophySimonetta Gerevini, Marina Scarlato, Lorenzo Maggi, et al.
Neuromuscular Disorders : NMD|February 14, 2017
Vocal cord paralysis in Charcot-Marie-Tooth type 4b1 disease associated with a novel mutation in the myotubularin-related protein 2 gene: A case report and review of the literatureAlberto Andrea Zambon, Maria Grazia Natali Sora, Giovanna Cantarella, et al.
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