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Article CommentaryBrain

Imaging of the 6-OPRI Mutation Prion Disease: An Entity Distinct from Typical Creutzfeldt-Jakob Disease?

A.J. Degnan and L.M. Levy
American Journal of Neuroradiology September 2013, 34 (9) 1731-1732; DOI: https://doi.org/10.3174/ajnr.A3490
A.J. Degnan
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L.M. Levy
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REFERENCES

  1. 1.↵
    1. De Vita E,
    2. Ridgway G,
    3. Scahill R,
    4. et al
    . Multi-parameter MRI in the 6-OPRI variant of inherited prion disease. AJNR Am J Neuroradiol 2013;34:1723–30
    Abstract/FREE Full Text
  2. 2.↵
    1. Lee H,
    2. Hoffman C,
    3. Kingsley PB,
    4. et al
    . Enhanced detection of diffusion reductions in Creutzfeldt-Jakob disease at a higher B factor. AJNR Am J Neuroradiol 2010;31:49–54
    Abstract/FREE Full Text
  3. 3.↵
    1. Breithaupt M,
    2. Romero C,
    3. Kallenberg K,
    4. et al
    . Magnetic resonance imaging in E200K and V210I mutations of the prion protein gene. Alzheimer Dis Assoc Disord 2013;27:87–90
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  4. 4.↵
    1. Zerr I,
    2. Kallenberg K,
    3. Summers DM,
    4. et al
    . Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease. Brain 2009;132:2659–68
    Abstract/FREE Full Text
  5. 5.↵
    1. Alner K,
    2. Hyare H,
    3. Mead S,
    4. et al
    . Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutation. J Neurol Neurosurg Psychiatry 2012;83:109–14
    Abstract/FREE Full Text
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American Journal of Neuroradiology: 34 (9)
American Journal of Neuroradiology
Vol. 34, Issue 9
1 Sep 2013
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Imaging of the 6-OPRI Mutation Prion Disease: An Entity Distinct from Typical Creutzfeldt-Jakob Disease?
A.J. Degnan, L.M. Levy
American Journal of Neuroradiology Sep 2013, 34 (9) 1731-1732; DOI: 10.3174/ajnr.A3490

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Imaging of the 6-OPRI Mutation Prion Disease: An Entity Distinct from Typical Creutzfeldt-Jakob Disease?
A.J. Degnan, L.M. Levy
American Journal of Neuroradiology Sep 2013, 34 (9) 1731-1732; DOI: 10.3174/ajnr.A3490
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