All Stories

  1. Targeted therapy of human glioblastoma via delivery of a toxin through a peptide directed to cell surface nucleolin
  2. Multiple spinal nerve enlargement and SOS1 mutation: Further evidence of overlap between neurofibromatosis type 1 and Noonan phenotype
  3. Impact of lysosomal storage disorders on biology of mesenchymal stem cells: Evidences from in vitro silencing of glucocerebrosidase (GBA) and alpha-galactosidase A (GLA) enzymes
  4. Rasagiline for sleep disorders in patients with Parkinson’s disease: a prospective observational study
  5. A novel diagnostic method to detect truncated neurofibromin in neurofibromatosis 1
  6. Foix-Chavany-Marie syndrome in a 17-year-old female with congenital cytomegalovirus infection
  7. Giant thrombosed intracavernous carotid artery aneurysm presenting as Tolosa–Hunt syndrome in a patient harboring a new pathogenic neurofibromatosis type 1 mutation: a case report and review of the literature