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

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Bibliographic Details
Published inJournal of neurology Vol. 264; no. 1; pp. 170 - 173
Main Authors Cistaro, A, Cassalia, L, Ferrara, C, Atzori, C, Vai, D, Quartuccio, N, Fania, P, Vaudano, G P, Imperiale, D
Format Report
LanguageEnglish
Published 01.01.2017
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Bibliography:ObjectType-Case Study-3
ObjectType-Correspondence-1
content type line 59
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ObjectType-Report-2
ISSN:1432-1459
DOI:10.1007/s00415-016-8327-5