Clinical, neuroimaging and genetic findings in children with hereditary ataxia: single center study
Article in Molecular Biology Reports (December 2022)
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Ataxia with oculomotor apraxia type 2 caused by a novel homozygous mutation in SETX gene, and literature review
Article in Frontiers in Molecular Neuroscience (November 2022)
Biological networks and complexity in early-onset motor neuron diseases
Article in Frontiers in Neurology (October 2022)