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Major or Mild Neurocognitive Disorder Due to Prion Disease

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References

Brown K, Mastrianni JA: The prion diseases. J Geriatr Psychiatry Neurol 23(4):277–298, 2010
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Chohan G, Pennington C, Mackenzie JM, et al: The role of cerebrospinal fluid 14-3-3 and other proteins in the diagnosis of sporadic Creutzfeldt-Jakob disease in the UK: a 10-year review. J Neurol Neurosurg Psychiatry 81(11):1243–1248, 2010
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Heath CA, Cooper SA, Murray K, et al: Validation of diagnostic criteria for variant Creutzfeldt-Jakob disease. Ann Neurol 67(6):761–770, 2010
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Ironside JW: Variant Creutzfeldt-Jakob disease: an update. Folia Neuropathol 50(1):50–56, 2012
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Ladogana A, Puopolo M, Croes EA, et al: Mortality from Creutzfeldt-Jakob disease and related disorders in Europe, Australia, and Canada. Neurology 64(9):1586–1591, 2005
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Prions: A model of conformational disease? Pathol Biol (Paris) 2014;():.doi:10.1016/j.patbio.2014.02.003.
 
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