Your browser doesn't support javascript.
loading
Brain 18F-FDG PET/CT findings in a case of genetic Creutzfeldt-Jakob disease due to V203I heterozygous mutation in the PRNP gene.
Cistaro, A; Cassalia, L; Ferrara, C; Atzori, C; Vai, D; Quartuccio, N; Fania, P; Vaudano, G P; Imperiale, D.
Affiliation
  • Cistaro A; Positron Emission Tomography Centre IRMET, S.p.A., Affidea, V. O. Vigliani 89, 10136, Turin, Italy. angelina.cistaro@affidea.it.
  • Cassalia L; Nuclear Medicine Unit, Department of Biomedical Sciences and of Mophologic and Functional Images, University of Messina, Messina, Italy.
  • Ferrara C; Nuclear Medicine Unit Department, P.O. Umberto I, Siracusa, Italy.
  • Atzori C; Neurology Unit and Human TSE Regional Center, ASL TO2 Maria Vittoria Hospital, Turin, Italy.
  • Vai D; Neurology Unit and Human TSE Regional Center, ASL TO2 Maria Vittoria Hospital, Turin, Italy.
  • Quartuccio N; Wolfson Molecular Imaging Centre, The University of Manchester, Manchester, UK.
  • Fania P; Positron Emission Tomography Centre IRMET, S.p.A., Affidea, V. O. Vigliani 89, 10136, Turin, Italy.
  • Vaudano GP; Neuroradiology Unit, ASL TO2 San Giovanni Bosco Hospital, Turin, Italy.
  • Imperiale D; Neurology Unit and Human TSE Regional Center, ASL TO2 Maria Vittoria Hospital, Turin, Italy.
J Neurol ; 264(1): 170-173, 2017 Jan.
Article in En | MEDLINE | ID: mdl-27844164
Subject(s)
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain / Creutzfeldt-Jakob Syndrome / Prion Proteins / Positron Emission Tomography Computed Tomography / Mutation Type of study: Diagnostic_studies Limits: Female / Humans / Middle aged Language: En Journal: J Neurol Year: 2017 Document type: Article
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain / Creutzfeldt-Jakob Syndrome / Prion Proteins / Positron Emission Tomography Computed Tomography / Mutation Type of study: Diagnostic_studies Limits: Female / Humans / Middle aged Language: En Journal: J Neurol Year: 2017 Document type: Article