All Stories

  1. Clinical and neurophysiological features of familial cortical myoclonic tremor with epilepsy
  2. Genetic analysis of the CHCHD2 gene in a cohort of Chinese patients with Parkinson disease
  3. Rational search for genes in familial cortical myoclonic tremor with epilepsy, clues from recent advances
  4. Depression in Parkinson's disease
  5. A pedigree of FCMTE1 in China
  6. Further evidence supports a fourth phenotype of PLA2G6-associated neurodegeneration
  7. BSCL2 S90L mutation in a Chinese family with Silver syndrome with a review of the literature
  8. Genetic analysis of SPG4 and SPG3A genes in a cohort of Chinese patients with hereditary spastic paraplegia
  9. First report of infantile ascending hereditary spastic paralysis in China
  10. chorea of the ears in Huntington's Disease
  11. Two cases of dural arteriovenous fistula presenting with parkinsonism and progressive cognitive dysfunction
  12. Cervical spinal cord compression caused by X-linked hypophosphatemic rickets with a novel PHEX mutation