• A family with Parkinsonism, essential tremor, restless legs syndrome, and depression
• Autophagy precedes apoptosis among at risk cerebellar Purkinje cells in the shaker mutant rat: an ultrastructural study
• Cellular density in the cerebellar molecular layer in essential tremor, spinocerebellar ataxia, and controls
• Cerebellar Atrophy in Cortical Myoclonic Tremor and Not in Hereditary Essential Tremor-a Voxel-Based Morphometry Study
• Clinical and genetic keys to cerebellar ataxia due to FGF14 GAA expansions
• Disease mechanism, biomarker and therapeutics for spinal and bulbar muscular atrophy (SBMA)
• Genetic analysis of ten common degenerative hereditary ataxia loci in patients with essential tremor
• Genetics of movement disorders-rare but important
• I¹²³-FP-CIT (DaTSCAN) SPECT beyond the Most Common Causes of Parkinsonism: A Systematic Review
• Inborn errors of copper metabolism
• Linkage exclusion in Italian families with hereditary essential tremor
• Mitochondrial serine protease HTRA2 p.G399S in a kindred with essential tremor and Parkinson disease
• Neurophysiology of cerebellar ataxias and gait disorders
• Non-Parkinson movement disorders: Five new things
• Specificity of transcranial sonography in parkinson spectrum disorders in comparison to degenerative cognitive syndromes
• SUMO-regulated mitochondrial function in Parkinson's disease
• Ultrasonographic (TCS) and clinical findings in overlapping phenotype of essential tremor and Parkinson's disease (ET-PD)
• Whole genome sequencing and rare variant analysis in essential tremor families