Marina Scarlato
Milan, Italy
Last Updated: 09/26/2026
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Found 39 publications
Immune-mediated necrotizing myopathies: clinico-serological features and treatment outcomes of a large Italian cohort of patients.
Journal: Journal of neurology
Published: May 04, 2026
Correction to: Daytime sleepiness and sleep quality in Charcot-Marie-Tooth disease.
Journal: Journal of neurology
Published: September 21, 2023
Overcoming therapeutic challenges: Successful management of a supposedly triple seronegative, refractory generalized myasthenia gravis patient with efgartigimod.
Journal: European journal of neurology
Published: August 25, 2023
Physical activity practiced at a young age is associated with a less severe subsequent clinical presentation in facioscapulohumeral muscular dystrophy.
Journal: BMC musculoskeletal disorders
Published: May 15, 2023
Daytime sleepiness and sleep quality in Charcot-Marie-Tooth disease.
Journal: Journal of neurology
Published: April 21, 2023
A smart tablet application to quantitatively assess the dominant hand dexterity.
Journal: Computer methods and programs in biomedicine
Published: April 03, 2023
Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxias.
Journal: American journal of human genetics
Published: March 26, 2023
Validation of a graphic test to quantitatively assess the dominant hand dexterity.
Journal: PloS one
Published: February 10, 2022
Clinical-Genetic Features Influencing Disability in Spastic Paraplegia Type 4: A Cross-sectional Study by the Italian DAISY Network.
Journal: Neurology. Genetics
Published: October 13, 2021
Loss of function MPZ mutation causes milder CMT1B neuropathy.
Journal: Journal of the peripheral nervous system : JPNS
Published: April 14, 2021
Out-of-Frame Mutations in ACTN2 Last Exon Cause a Dominant Distal Myopathy With Facial Weakness.
Journal: Neurology. Genetics
Published: March 15, 2021
Last Updated: 09/26/2026