← Evidence map

ArticleJournal of neurology2017

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

A Cistaro et al.PubMed ↗Publisher ↗

No numbers read from the abstract.

5 papers cite it

2017
2018
2019
2020
2021
2022
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 27844164