All Stories

  1. ASO-enhancement ofTARDBPexitron splicing mitigates TDP-43 proteinopathies
  2. Validation study of the Japanese version of the King's Parkinson's Disease Pain Scale and the King's Parkinson's Disease Pain Questionnaire
  3. Neuronal Intranuclear Inclusion Disease Presenting with Voice Tremor
  4. Brain calcification in a CSF1R mutation carrier precedes white matter degeneration
  5. Cerebral peduncle angle: Unreliable in differentiating progressive supranuclear palsy from other neurodegenerative diseases
  6. Clinical and genetic characterization of adult-onset leukoencephalopathy with axonal spheroids and pigmented glia associated withCSF1Rmutation
  7. Diagnostic Value of Brain Calcifications in Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia
  8. Characteristic microglial features in patients with hereditary diffuse leukoencephalopathy with spheroids
  9. Deep brain stimulation for levodopa-refractory benign tremulous parkinsonism
  10. Hypertrophic olivary degeneration: A clinico-radiologic study
  11. Heterogeneity of cerebral TDP-43 pathology in sporadic amyotrophic lateral sclerosis: Evidence for clinico-pathologic subtypes
  12. Increased cytoplasmicTARDBPmRNA in affected spinal motor neurons in ALS caused by abnormal autoregulation of TDP-43
  13. Autosomal dominant Parkinson's disease caused by SNCA duplications
  14. Familial idiopathic basal ganglia calcification: Histopathologic features of an autopsied patient with anSLC20A2mutation
  15. Variable expression of microglial DAP12 and TREM2 genes in Nasu-Hakola disease
  16. C9ORF72repeat-associated non-ATG-translated polypeptides are distributed independently of TDP-43 in a Japanese patient with c9ALS
  17. A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories
  18. Bunina bodies in motor and non-motor neurons revisited: A pathological study of an ALS patient after long-term survival on a respirator
  19. Haploinsufficiency of CSF-1R and clinicopathologic characterization in patients with HDLS
  20. A Japanese family with idiopathic basal ganglia calcification with novel SLC20A2 mutation presenting with late-onset hallucination and delusion
  21. Japanese amyotrophic lateral sclerosis patients with GGGGCC hexanucleotide repeat expansion in C9ORF72