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Gabriella Silvestri

The Catholic University of America

4

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53

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Dysregulation of Circular RNAs in Myotonic Dystrophy Type 1

2019 International Journal of Molecular Sciences
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Severe 5,10-methylenetetrahydrofolate reductase deficiency: A rare, treatable cause of complicated hereditary spastic paraplegia

2018 European Journal of Neurology
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Hereditary spastic paraplegia: a novel mutation and expansion of the phenotype variability in SPG10

2015 Journal of Neurology, Neurosurgery, and Psychiatry
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Prevalence of spinocerebellar ataxia type 2 mutation among Italian Parkinsonian patients

2007 Movement Disorders
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