Alessandra Govoni
Milan, Italy
Last Updated: 09/26/2026
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Found 36 publications
Characterization of Phenotypic Variability in Becker Muscular Dystrophy for Clinical Practice and Towards Trial Readiness: A Two-Years Follow up Study.
Journal: Journal of neuromuscular diseases
Published: January 08, 2024
Respiratory function in a large cohort of treatment-naïve adult spinal muscular atrophy patients: a cross-sectional study.
Journal: Neuromuscular disorders : NMD
Published: September 03, 2023
Proposal of a new clinical protocol for evaluating fatigability in adult SMA patients.
Journal: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology
Published: August 22, 2023
Multi-omics profiling of CSF from spinal muscular atrophy type 3 patients after nusinersen treatment: a 2-year follow-up multicenter retrospective study.
Journal: Cellular and molecular life sciences : CMLS
Published: April 02, 2023
Phenotypic characterization of c.379A > G GJB1 mutation in a Charcot-Marie-Tooth female patient.
Journal: Acta neurologica Belgica
Published: May 15, 2022
Bridging the Gap: Gene Therapy in a Patient With Spinal Muscular Atrophy Type 1.
Journal: Neurology
Published: April 24, 2022
Adults with spinal muscular atrophy: a large-scale natural history study shows gender effect on disease.
Journal: Journal of neurology, neurosurgery, and psychiatry
Published: March 25, 2022
CACNA1S mutation associated with a case of juvenile-onset congenital myopathy.
Journal: Journal of the neurological sciences
Published: August 27, 2021
Molecular analysis of SMARD1 patient-derived cells demonstrates that nonsense-mediated mRNA decay is impaired.
Journal: Journal of neurology, neurosurgery, and psychiatry
Published: February 17, 2021
Early Findings in Neonatal Cases of RYR1-Related Congenital Myopathies.
Journal: Frontiers in neurology
Published: February 05, 2021
Last Updated: 09/26/2026