Luca Bartesaghi
Stockholm, AB, Sweden
Last Updated: 09/26/2026
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Found 15 publications
Exploring the effect of red and near-infrared light on neurodegenerative disease: A focus on amyotrophic lateral sclerosis, Charcot's devastating disease of the motor system.
Journal: International review of neurobiology
Published: August 18, 2026
Tight Spaces, Tighter Signals: Spatial Constraints as Drivers of Peripheral Myelination.
Journal: Cells
Published: April 30, 2025
Structural insights into Charcot-Marie-Tooth disease-linked mutations in human GDAP1.
Journal: FEBS open bio
Published: February 28, 2022
Erratum to: Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia.
Journal: Brain : a journal of neurology
Published: May 13, 2021
Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia.
Journal: Brain : a journal of neurology
Published: July 24, 2020
Disrupted function of lactate transporter MCT1, but not MCT4, in Schwann cells affects the maintenance of motor end-plate innervation.
Journal: Glia
Published: December 31, 2019
Altered interplay between endoplasmic reticulum and mitochondria in Charcot-Marie-Tooth type 2A neuropathy.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: January 20, 2019
Characterization of molecular mechanisms underlying the axonal Charcot-Marie-Tooth neuropathy caused by MORC2 mutations.
Journal: Human molecular genetics
Published: November 20, 2018
PRDM12 Is Required for Initiation of the Nociceptive Neuron Lineage during Neurogenesis.
Journal: Cell reports
Published: October 12, 2018
Loss of tubulin deglutamylase CCP1 causes infantile-onset neurodegeneration.
Journal: The EMBO journal
Published: August 22, 2018
Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremor.
Journal: Human molecular genetics
Published: May 29, 2015
Last Updated: 09/26/2026