Disease: Pallidopyramidal syndrome
- 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