Roberto Massa
Rome, 00133, Italy
Last Updated: 09/26/2026
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Found 80 publications
Correction to: Italian recommendations for the diagnosis and treatment of myasthenia gravis.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: May 08, 2026
Italian recommendations for the diagnosis and treatment of myasthenia gravis.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: December 26, 2025
The novel (TCTG)n motif in CNBP expanded alleles: composition, dynamics and genotype-phenotype correlation in Myotonic dystrophy type 2 (DM2).
Journal: Human genomics
Published: December 22, 2025
Landscape Analysis of COL6A1, COL6A2, and COL6A3 Pathogenic Variants in a Large Italian Cohort Presenting with Collagen VI-Related Myopathies: A Nationwide Report.
Journal: Biomolecules
Published: July 14, 2025
Clinical, Histopathologic, and Genetic Features of Patients With Myofibrillary and Distal Myopathies: Experience From the Italian Network.
Journal: Neurology
Published: August 05, 2024
Changes in body composition revealed by bioelectrical impedance analysis reflect strength and motor performance in myotonic dystrophy type 2.
Journal: Frontiers in neurology
Published: June 19, 2024
Integrating D4Z4 methylation analysis into clinical practice: improvement of FSHD molecular diagnosis through distinct thresholds for 4qA/4qA and 4qA/4qB patients.
Journal: Clinical epigenetics
Published: June 18, 2024
Trimetazidine Improves Mitochondrial Dysfunction in SOD1G93A Cellular Models of Amyotrophic Lateral Sclerosis through Autophagy Activation.
Journal: International journal of molecular sciences
Published: January 24, 2024
Comprehensive Cardiovascular Management of Myotonic Dystrophy Type 1 Patients: A Report from the Italian Neuro-Cardiology Network.
Journal: Journal of cardiovascular development and disease
Published: January 01, 2024
In Cis Effect of DMPK Expanded Alleles in Myotonic Dystrophy Type 1 Patients Carrying Variant Repeats at 5' and 3' Ends of the CTG Array.
Journal: International journal of molecular sciences
Published: April 17, 2023
Using Cluster Analysis to Overcome the Limits of Traditional Phenotype-Genotype Correlations: The Example of RYR1-Related Myopathies.
Journal: Genes
Published: November 25, 2022
NEFL-Related Charcot-Marie Tooth Disease due to P440L Mutation in Two Italian Families: Expanding the Phenotype and Defining Modulating Factors.
Journal: European neurology
Published: October 13, 2022
Last Updated: 09/26/2026