@article{IR,
      author = {Alrohaibani, Alaaeddin and Woltjer, Randall},
      url = {http://digitalcollections.ohsu.edu/record/8346},
      title = {Sporadic fatal insomnia: a case report},
      publisher = {Oregon Health and Science University},
      abstract = {The most common prion disease is Creutzfeldt-Jacob disease  (CJD), usually sporadic (sCJD), but in up to 15% familial  due to mutations in the prion gene. CJD presents with  myoclonis, ataxia, and rapidly progressive dementia with an  average age of onset of 67 years. Fatal Familial Insomnia  (FFI) is a related uniformly fatal prion disease, with mean  onset of dysautonomia and insomnia at 56 years and mean  duration of 13 months.},
      number = {IR},
      doi = {https://doi.org/10.6083/gb19f633j},
      recid = {8346},
      address = {2020},
}