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  1. Correction: Sciacca, F. L., et al. Microduplication of 15q13.3 and Microdeletion of 18q21.32 in a Patient with Moyamoya Syndrome. Int. J. Mol. Sci. 2018, 19, 3675
  2. Microduplication of 15q13.3 and Microdeletion of 18q21.32 in a Patient with Moyamoya Syndrome
  3. Period3 gene in disorder of consciousness: The role of neuroimaging in understanding the relationship between genotype and sleep. A brief communication
  4. Transcriptional role of androgen receptor in the expression of long non-coding RNA Sox2OT in neurogenesis
  5. Autocrine release of angiopoietin-2 mediates cerebrovascular disintegration in Moyamoya disease
  6. Fabry Disease: Recognition, Diagnosis, and Treatment of Neurological Features
  7. The diagnostic challenge of Divry van Bogaert and Sneddon Syndrome: Report of three cases and literature review
  8. Vasculogenic and Angiogenic Pathways in Moyamoya Disease
  9. Research Progresses in Understanding the Pathophysiology of Moyamoya Disease
  10. Per3 gene and disorders of consciousness
  11. Human Adipose-Derived Mesenchymal Stem Cells as a New Model of Spinal and Bulbar Muscular Atrophy
  12. Decellularized silk fibroin scaffold primed with adipose mesenchymal stromal cells improves wound healing in diabetic mice
  13. MEF2C deletions and mutations versus duplications: A clinical comparison
  14. An autoinflammatory neurological disease due to interleukin 6 hypersecretion