All Stories

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