Brain 18F-FDG PET/CT findings in a case of genetic Creutzfeldt-Jakob disease due to V203I heterozygous mutation in the PRNP gene

J Neurol. 2017 Jan;264(1):170-173. doi: 10.1007/s00415-016-8327-5. Epub 2016 Nov 14.

¹ Positron Emission Tomography Centre IRMET, S.p.A., Affidea, V. O. Vigliani 89, 10136, Turin, Italy. [email protected].
² Nuclear Medicine Unit, Department of Biomedical Sciences and of Mophologic and Functional Images, University of Messina, Messina, Italy.
³ Nuclear Medicine Unit Department, P.O. Umberto I, Siracusa, Italy.
⁴ Neurology Unit and Human TSE Regional Center, ASL TO2 Maria Vittoria Hospital, Turin, Italy.
⁵ Wolfson Molecular Imaging Centre, The University of Manchester, Manchester, UK.
⁶ Positron Emission Tomography Centre IRMET, S.p.A., Affidea, V. O. Vigliani 89, 10136, Turin, Italy.
⁷ Neuroradiology Unit, ASL TO2 San Giovanni Bosco Hospital, Turin, Italy.

No abstract available

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