• A novel FBXO7-R345P mutation in a Chinese family with autosomal recessive parkinsonian-pyramidal syndrome
• Advances in the Clinical Differential Diagnosis of Parkinson's Disease
• C19orf12 mutation leads to a pallido-pyramidal syndrome
• Compound heterozygous variants of the FBXO7 gene resulting in infantile-onset Parkinsonian-pyramidal syndrome in siblings of a Chinese family
• Early-onset autosomal-recessive parkinsonian-pyramidal syndrome
• Expanding the Spectrum of Dopa-Responsive Dystonia (DRD) and Proposal for New Definition: DRD, DRD-plus, and DRD Look-alike
• F-box only protein 7 gene in parkinsonian-pyramidal disease
• First Case of Parkinsonian-Pyramidal Syndrome Associated with a TBK1 Mutation
• G51D α-synuclein mutation causes a novel parkinsonian-pyramidal syndrome
• Hypomyelination with Atrophy of the Basal Ganglia and Cerebellum (H-ABC) is a Differential Diagnosis for Pallidopyramidal Syndromes with Thin Corpus Callosum
• Is Pallido-Pyramidal Syndrome Still a Useful Concept? No
• Is Pallido-Pyramidal Syndrome Still a Useful Concept? Yes
• Mechanistic contributions of FBXO7 to Parkinson disease
• Novel compound heterozygous FBXO7 mutations in a family with early onset Parkinson's disease
• Pallidal degenerations and related disorders: an update
• PARK15/FBXO7 is dispensable for PINK1/Parkin mitophagy in iNeurons and HeLa cell systems
• Parkinsonian-Pyramidal syndromes: A systematic review
• Pathophysiological mechanisms linking F-box only protein 7 (FBXO7) and Parkinson's disease (PD)
• Psychiatric Manifestations of <em>ATP13A2</em> Mutations
• The Downregulation of <em>c19orf12</em> Negatively Affects Neuronal and Musculature Development in Zebrafish Embryos
• The pallidopyramidal syndromes: nosology, aetiology and pathogenesis