All Stories

  1. Deletion of P2 promoter of GJB1 gene a cause of Charcot-Marie-Tooth disease
  2. Spinal cord infarction in a sick neonate from predominant haemorrhagic aetiology: a case report
  3. Long-term outcome of paediatric spinal cord injury
  4. A novel MYH2 mutation in family members presenting with congenital myopathy, ophthalmoplegia and facial weakness
  5. Brain Abscesses Due to Citrobacter koseri in a Pair of Twins