Factors predictive of the presence of a CSF1R mutation in patients with leukoencephalopathy

Ítems similars

• Mutations in the colony stimulating factor 1 receptor (CSF1R) cause hereditary diffuse leukoencephalopathy with spheroids
  per: Rademakers, Rosa, et al.
  Publicat: (2011)
• CSF1R mutations in hereditary diffuse leukoencephalopathy with spheroids are loss of function
  per: Pridans, Clare, et al.
  Publicat: (2013)
• Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutations
  per: Sundal, Christina, et al.
  Publicat: (2013)
• Clinical and genetic characterization of adult‐onset leukoencephalopathy with axonal spheroids and pigmented glia associated with CSF1R mutation
  per: Konno, T., et al.
  Publicat: (2016)
• Diagnostic Criteria for Adult-onset Leukoencephalopathy With Axonal Spheroids and Pigmented Glia Due to CSF1R mutation
  per: Konno, Takuya, et al.
  Publicat: (2017)