Alessandra Bolino
Milan, 20132, Italy
Last Updated: 09/26/2026
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Found 32 publications
PIK3CA gain-of-function mutation in Schwann cells leads to severe neuropathy and aerobic glycolysis through a non-cell autonomous effect.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: June 24, 2025
Regulation of Schwann Cell-Axon Interactions in Nerve Development: The Role of Slit2 in Axonal Sorting.
Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience
Published: February 27, 2025
Disease Progression in Charcot-Marie-Tooth Disease Type 4B (CMT4B) Associated With Mutations in Myotubularin-Related Proteins 2 and 13.
Journal: European journal of neurology
Published: October 28, 2024
Genotype and phenotype spectrum of Charcot-Marie-Tooth disease due to mutations in SORD.
Journal: Brain : a journal of neurology
Published: June 08, 2024
Correction: Molecular mechanisms and therapeutic strategies for neuromuscular diseases.
Journal: Cellular and molecular life sciences : CMLS
Published: June 03, 2024
Niacin ameliorates Charcot-Marie-Tooth 4B1 neuropathy without interfering with nerve regeneration.
Journal: Brain communications
Published: March 07, 2024
Molecular mechanisms and therapeutic strategies for neuromuscular diseases.
Journal: Cellular and molecular life sciences : CMLS
Published: January 02, 2024
Recent advances in the treatment of Charcot-Marie-Tooth neuropathies.
Journal: Journal of the peripheral nervous system : JPNS
Published: December 28, 2022
Mutations in MYO9B are associated with Charcot-Marie-Tooth disease type 2 neuropathies and isolated optic atrophy.
Journal: European journal of neurology
Published: October 04, 2022
Therapeutic advantages of combined gene/cell therapy strategies in a murine model of GM2 gangliosidosis.
Journal: Molecular therapy. Methods & clinical development
Published: December 27, 2021
Myelin Biology.
Journal: Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics
Published: June 28, 2021
Dysregulation of myelin synthesis and actomyosin function underlies aberrant myelin in CMT4B1 neuropathy.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: March 03, 2021
Last Updated: 09/26/2026